Zazzle Shop

Screen printing
Showing posts with label Genetic Engineering. Show all posts
Showing posts with label Genetic Engineering. Show all posts

Friday, June 10, 2011

Chinese GM Cows Make Human Breast Milk

Holly Williams, Beijing correspondent

Dairy cows

Chinese scientists say human breast milk produced by cows is more nutritious than normal milk. Picture: AFP


Chinese scientists have genetically modified dairy cows to produce human breast milk, and hope to be selling it in supermarkets within three years.



The milk produced by the transgenic cows is identical to the human variety and has the same immune-boosting and antibacterial qualities as breast milk, scientists at China's Agricultural University in Beijing say.

The transgenic herd of 300 was bred by inserting human genes into cloned cow embryos which were then implanted into surrogate cows.

The technology was similar to that used to produce Dolly the sheep.

The milk is still undergoing safety tests but with government permission it will be sold to consumers as a more nutritious dairy drink than cow's milk.

Workers at the university's dairy farm have already tasted the milk, and say it is sweeter and stronger than the usual bovine variety.

There are 1.5 billion people in the world who don't get enough to eat. It's our duty to develop science and technology, not to hold it back. We need to feed people first, before we consider ideals and convictions.

Professor Li Ning, director of the research project

"It's good," said worker Jiang Yao. "It's better for you because it's genetically modified."

The scientists have also produced animals that are resistant to mad cow disease, as well as beef cattle that are genetically modified to produce more nutritious meat.

The director of the research project, Professor Li Ning, says Western concerns about the ethics of genetic modification are misplaced.

"There are 1.5 billion people in the world who don't get enough to eat," he said. "It's our duty to develop science and technology, not to hold it back.

"We need to feed people first, before we consider ideals and convictions."

In contrast to Europe, China has eagerly embraced genetically modified food.

GM cooking oil, papayas, tomatoes and potatoes are already widely available.

Insect-resistant rice and corn modified to help pigs absorb more nutrients were both recently approved by the government.

Monday, April 4, 2011

Genetically modified cows produce 'human' milk

From: http://www.telegraph.co.uk/

Scientists have created genetically modified cattle that produce "human" milk in a bid to make cows' milk more nutritious.

Scientists have created genetically modified cattle that produce human milk in a bid to make cows' milk more nutritious.
Researchers say they are able to create cows that produce milk containing a human protein called lysozyme Photo: PA

The scientists have successfully introduced human genes into 300 dairy cows to produce milk with the same properties as human breast milk.

Human milk contains high quantities of key nutrients that can help to boost the immune system of babies and reduce the risk of infections.

The scientists behind the research believe milk from herds of genetically modified cows could provide an alternative to human breast milk and formula milk for babies, which is often criticised as being an inferior substitute.

They hope genetically modified dairy products from herds of similar cows could be sold in supermarkets. The research has the backing of a major biotechnology company.

The work is likely to inflame opposition to GM foods. Critics of the technology and animal welfare groups reacted angrily to the research, questioning the safety of milk from genetically modified animals and its effect on the cattle's health.

But Professor Ning Li, the scientist who led the research and director of the State Key Laboratories for AgroBiotechnology at the China Agricultural University insisted that the GM milk would be as safe to drink as milk from ordinary dairy cows.

He said: "The milk tastes stronger than normal milk.

“We aim to commercialize some research in this area in coming three years. For the “human-like milk”, 10 years or maybe more time will be required to finally pour this enhanced milk into the consumer’s cup.”

China is now leading the way in research on genetically modified food and the rules on the technology are more relaxed than those in place in Europe.

The researchers used cloning technology to introduce human genes into the DNA of Holstein dairy cows before the genetically modified embryos were implanted into surrogate cows.

Writing in the scientific peer-reviewed journal Public Library of Science One, the researchers said they were able to create cows that produced milk containing a human protein called lysozyme,

Lysozyme is an antimicrobial protein naturally found in large quantities in human breast milk. It helps to protect infants from bacterial infections during their early days of life.

They created cows that produce another protein from human milk called lactoferrin, which helps to boost the numbers of immune cells in babies. A third human milk protein called alpha-lactalbumin was also produced by the cows.

The scientists also revealed at an exhibition at the China Agricultural University that they have boosted milk fat content by around 20 per cent and have also changed the levels of milk solids, making it closer to the composition of human milk as well as having the same immune-boosting properties.

Professor Li and his colleagues, who have been working with the Beijing GenProtein Biotechnology Company, said their work has shown it was possible to "humanise" cows milk.

In all, the scientists said they have produced a herd of around 300 cows that are able to produce human-like milk.

The transgenic animals are physically identical to ordinary cows.

Writing in the journal, Professor Li said: "Our study describes transgenic cattle whose milk offers the similar nutritional benefits as human milk.

"The modified bovine milk is a possible substitute for human milk. It fulfilled the conception of humanising the bovine milk."

Speaking to The Sunday Telegraph, he added the “human-like milk” would provide “much higher nutritional content”. He said they had managed to produce three generations of GM cows but for commercial production there would need to be large numbers of cows produced.

He said: “Human milk contains the ‘just right’ proportions of protein, carbohydrates, fats, minerals, and vitamins for an infant’s optimal growth and development.

“As our daily food, the cow’s milk provided us the basic source of nutrition. But the digestion and absorption problems made it not the perfect food for human being."

The researchers also insist having antimicrobial proteins in the cows milk can also be good for the animals by helping to reduce infections of their udders.

Genetically modified food has become a highly controversial subject and currently they can only be sold in the UK and Europe if they have passed extensive safety testing.

The consumer response to GM food has also been highly negative, resulting in many supermarkets seeking to source products that are GM free.

Campaigners claim GM technology poses a threat to the environment as genes from modified plants can get into wild plant populations and weeds, while they also believe there are doubts about the safety of such foods.

Scientists insist genetically modified foods are unlikely to pose a threat to food safety and in the United States consumers have been eating genetically modified foods for more decades.

However, during two experiments by the Chinese researchers, which resulted in 42 transgenic calves being born, just 26 of the animals survived after ten died shortly after birth, most with gastrointestinal disease, and a further six died within six months of birth.

Researchers accept that the cloning technology used in genetic modification can affect the development and survival of cloned animals, although the reason why is not well understood.

A spokesman for the Royal Society for the Protection of Animals said the organisation was "extremely concerned" about how the GM cows had been produced.

She said: "Offspring of cloned animals often suffer health and welfare problems, so this would be a grave concern.

"Why do we need this milk – what is it giving us that we haven't already got."

Helen Wallace, director of biotechnology monitoring group GeneWatch UK, said: "We have major concerns about this research to genetically modify cows with human genes.

"There are major welfare issues with genetically modified animals as you get high numbers of still births.

"There is a question about whether milk from these cows is going to be safe from humans and it is really hard to tell that unless you do large clinical trials like you would a drug, so there will be uncertainty about whether it could be harmful to some people.

"Ethically there are issues about mass producing animals in this way."

Professor Keith Campbell, a biologist at the University of Nottingham works with transgenic animals, said: "Genetically modified animals and plants are not going to be harmful unless you deliberately put in a gene that is going to be poisonous. Why would anyone do that in a food?

"Genetically modified food, if done correctly, can provide huge benefit for consumers in terms of producing better products."

Thursday, December 23, 2010

'Singing Mouse' Made With Genetic Modification

From: http://news.discovery.com/

The tweeting mouse, created by triggering mutations, could help shed light on how language evolved.

Content provided by AFP

tweeting mouse
Japanese scientists said they have produced a mouse that tweets like a bird in a genetically engineered "evolution." Click to enlarge this image.

Osaka University

Japanese scientists said Tuesday they had produced a mouse that tweets like a bird in a genetically engineered "evolution" which they hope will shed light on the origins of human language.
A team of researchers at the University of Osaka created the animal in their "Evolved Mouse Project," in which they use genetically modified mice that are prone to miscopying DNA and thus to mutations.
"Mutations are the driving force of evolution. We have cross-bred the genetically modified mice for generations to see what would happen," lead researcher Arikuni Uchimura said.
"We checked the newly born mice one by one... One day we found a mouse that was singing like a bird," he said, noting that the "singing mouse" was born by chance but that the trait will be passed on to future generations.
Click here to see and hear the singing mouse.
"I was surprised because I had been expecting mice that are different in physical shape," he said by telephone, adding that in fact the project had also produced "a mouse with short limbs and a tail like a dachshund."
The laboratory, directed by professor Takeshi Yagi at the Osaka University's Graduate School of Frontier Biosciences in western Japan, now has more than 100 "singing mice" for further research.

The team hopes they will provide clues on how human language evolved, just as researchers in other countries study songbirds such as finches to help them understand the origins of human language.

Scientists have found that birds use different sound elements, put them together into chunks like words in human languages and then make strings of them to sing "songs," that are subject to certain linguistic rules.
"Mice are better than birds to study because they are mammals and much closer to humans in their brain structures and other biological aspects," Uchimura said.

"We are watching how a mouse that emits new sounds would affect ordinary mice in the same group... in other words if it has social connotations," he said, adding that ordinary mice squeak mainly under stress.
Considering that mutant mice tweet louder when put in different environments or when males are put together with females, Uchimura said their chirps "may be some sort of expressions of their emotions or bodily conditions."

The team has found that ordinary mice that grew up with singing mice emitted fewer ultrasounds than others, which could indicate that communication methods can spread in the same group like a dialect.
Uchimura dreams of further "evolution" of mice through genetic engineering.
"I know it's a long shot and people would say it's 'too absurd'... but I'm doing this with hopes of making a Mickey Mouse some day," he said.

Wednesday, June 16, 2010

Israel plows new ground in exotic crops

A tomato breeder has created a crop worth more than its weight in gold. The seeds for the yellow cherry tomato, a fruit researchers feared might turn off consumers, now sell for $160,000 a pound.

By Edmund Sanders,
From: Los Angeles Times

  • Edmund Sanders, Los Angeles Times

Reporting from Berurim, Israel — —

If Willy Wonka had a farm, it would fit right in here in Israel.

Want a lemon-scented tomato or a chocolate-colored persimmon? How about some miniaturized garlic cloves for the home chef who doesn't have time to chop, or a purple potato that tastes buttery when cooked?

There are no chocolate rivers or edible teacup flowers on Israeli farms, but you will find carrots shaped like potatoes, strawberries shaped like carrots, star-shaped zucchini and "watermelon" tomatoes — dark green on the outside with a juicy red flesh.

There are also specially bred red peppers with three times the usual amount of vitamins, and black chickpeas with extra antioxidants. Not to mention worm-shaped berries and blue bananas.

Though some mock such colorful crops as "frankenfruit," an Israeli tomato breeder, Hazera Genetics, has created a boutique crop worth more than its weight in gold.

The former kibbutz supplier developed a yellow cherry tomato that its own researchers feared might turn off consumers. Instead, the hybrid became a hit in Europe, where the seeds sell for about $160,000 a pound.

Bolstered by Hazera's success, a growing number of Israeli farmers, agricultural companies and government-funded research institutions are jumping into the market for freaky fruits and designer veggies, hoping to stumble upon the next big thing.

"It's fun, it's interesting and it brings in the customers," said Uri Rabinowitz, a Tel Aviv-area farmer who has developed a national following for his strange-looking crops, including elongated strawberries and round carrots. "You can charge twice as much."

Rabinowitz and other Israeli farmers grow exotic fruits and vegetables from imported seeds, including the chocolaty persimmon from Latin America (which makes a tasty ice cream) and the buttery potato from the Netherlands.

Some are trying to create new foods in the lab. A team of Israeli and U.S. scientists created the lemon-scented tomato by splicing genes from lemon basil into tomatoes, producing an aroma and taste of lemons and roses.

Efraim Lewinsohn, who has helped lead the project to develop the lemon tomato at Israel's Volcani Agricultural Research Institute, said the goal was to inject a little spice into tomatoes that had become bland from years of mass production.

"People complain that tomatoes don't taste like they used to," Lewinsohn said. "That's the driving force behind this project: attempting to restore the flavor of the past."

Tuesday, June 15, 2010

Amazed Boffins Probe Ozzy's Genetic Code

Elizabeth Scott,
Sky News Online

Scientists are to map Ozzy Osbourne's genetic code in a bid to find out how he is still alive after decades of drug and alcohol abuse.

Ozzy Osbourne

Hard-living Ozzy Osbourne has admitted abusing drink and drugs for 40 years

The former Black Sabbath frontman is only one of a few people in the world to have his full genome analysed.

It is hoped the results from the £27,000 test, which takes three months, will provide information on how drugs are absorbed in the body.

Ozzy, 61, has lived a life that would presumably kill any ordinary person.

Even the singer himself cannot understand how he has survived this long, recently describing himself as a "medical miracle" after going on a "bender" for "40 years".

He has admitted drinking four bottles of cognac a day at one point, "blacking out, coming to again and carrying on".

Ozzy and Sharon Osbourne

Ozzy Osbourne with wife Sharon, who he once tried to strangle

Ozzy famously bit the head off a rat while performing with Black Sabbath and in 2003 broke his neck in a quad bike accident.

He also has a genetic disorder similar to Parkinson's disease and on at least one occasion has been committed to a mental institution.

Despite all his excesses, he is still with wife Sharon, who he once tried to strangle, and the couple have three grown-up children.

Now he may get some answers from US company Knome, which will use a blood sample to map his genome.

Nathan Pearson, director of research at the firm, said: "Sequencing and analysing individuals with extreme medical histories provides the greatest potential scientific value."

The results will hopefully help scientists understand why the bodies of hard-living rockers such as Ozzy, Keith Richards, Ronnie Wood and Iggy Pop are able to take more substance abuse than the average person.

Wednesday, June 2, 2010

Scientists breed goats that produce spider silk

by Lisa Zyga
from: http://www.physorg.com/

goat  silk

Enlarge

Goats that produce spider silk protein in their milk could enable researchers to collect large quantities of the silk. Image credit: National Science Foundation.

(PhysOrg.com) -- Researchers from the University of Wyoming have developed a way to incorporate spiders' silk-spinning genes into goats, allowing the researchers to harvest the silk protein from the goats’ milk for a variety of applications. For instance, due to its strength and elasticity, spider silk fiber could have several medical uses, such as for making artificial ligaments and tendons, for eye sutures, and for jaw repair. The silk could also have applications in bulletproof vests and improved car airbags.

Normally, getting enough for these applications requires large numbers of spiders. However, spiders tend to be territorial, so when the researchers tried to set up spider farms, the spiders killed each other.

To solve this problem, Randy Lewis, a professor of at the University of Wyoming, and other researchers decided to put the spiders’ dragline silk gene into goats in such a way that the goats would only make the in their milk. Like any other genetic factor, only a certain percentage of the goats end up with the gene. For instance, of seven goat kids born in February 2010, three have tested positive for having the silk protein gene. When these transgenic goats have kids and start lactating, the researchers will collect the milk and purify the spider silk protein into “much, much higher quantities,” Lewis said.

Other than their ability to produce the silk protein, the goats do not seem to have any other differences in health, appearance, or behavior compared to goats without the gene, the researchers said.

In the future, the scientists plan to incorporate the silk into alfalfa plants, which they say could produce even larger quantities of silk. They explain that not only is alfalfa widely distributed, it also has a high (20-25%) protein content, making it an ideal crop to produce silk protein.

More information: via: National Science Foundation

© 2010 PhysOrg.com

Wednesday, March 17, 2010

Humans could regrow body parts like some amphibians

Regrowing amputated limbs, broken backs and even damaged brains could one day be a reality after scientists discovered a gene that is key to the almost magical ability.

Researchers have found that the gene p21 appears to block the healing power still enjoyed by some creatures including amphibians but lost through evolution to all other animals.

By turning off p21, the process can be miraculously switched back on.

Academics from The Wistar Institute in Philadelphia found that mice lacking the p21 gene gain the ability to regenerate lost or damaged tissue.

Unlike typical mammals, which heal wounds by forming a scar, these mice begin by forming a blastema, a structure associated with rapid cell growth.

According to the Wistar researchers, the loss of p21 causes the cells of these mice to behave more like regenerating embryonic stem cells rather than adult mammalian cells. This means they act as if they creating rather thane mending the body.

Their findings, published in the Proceedings of the National Academy of Sciences, provide solid evidence to link tissue regeneration to the control of cell division.

They turned off the gene in mice which had damaged ears and they regrew them. While they say it is early days, there is nothing theoretically different about applying the same process to humans.

Professor Ellen Heber-Katz, the lead scientist, said: "Much like a newt that has lost a limb, these mice will replace missing or damaged tissue with healthy tissue that lacks any sign of scarring.

"While we are just beginning to understand the repercussions of these findings, perhaps, one day we'll be able to accelerate healing in humans by temporarily inactivating the p21 gene.

"In normal cells, p21 acts like a brake to block cell cycle progression in the event of DNA damage, preventing the cells from dividing and potentially becoming cancerous.

"We propose that any future therapy would involve turning off p21 transiently during the healing process and only locally at the wound site. This might be done through locally applied drugs. This should minimise any side effects."

Wednesday, September 23, 2009

7 Intriguing Genetically Modified Fruits & VeggiesS

By Ecoist

montagefruitvegg-copy

Genetically modified food is one of great controversies of our time. Supporters point to wonderful possibilities of nutrient-packed food and solving world hunger, while critics fear unknown effects on human health. But whatever one’s opinion the matter, one thing is clear: some genetically modified fruits and vegetables are awfully intriguing! Here are 7 of the most interesting examples:

Graisins

graisin

(Image via Elanso)

The graisin (or giant raisin) is a raisin which has been genetically re-programmed to grow far beyond its normal size. It was produced by Japan’s National Institute of Genetics, which is unsurprising given that nation’s love for large fruits of all kinds. And while they taste exactly the same as small raisins, graisins are sure to make dinner guests stare in awe!

Grapples

grapple

(Image via Wikipedia)

Originally funded by UNICEF and created for Third World aid efforts, a grapple is simply a genetic cross between a grape and an apple. The fruit keeps the size and shape of the apple, the texture of the grape, and the flavor of both while providing a potent, high-strength dose of vitamin C.

Pluots

pluot

(Image via Palomar.edu)

Plums and apricots are delicious fruits in their own right, but combined, they form the genetically modified treat known as the pluot. Described by WiseGeek as “an intensely flavored fruit”, pluots are heavily fortified with vitamin C and have no sodium or cholesterol.

Tangelo

tangelo

(Image via TeamSugar)

“Should I have a tangerine or a grapefruit?” No longer need this question be asked! Lovers of each fruit can now get the best of both worlds with this sweet hybrid, which boasts a ton of fiber, vitamin C, and a slightly tart taste!

Colorful carrots

carrots

(Image via MSNBC)

Could colorful, genetically-modified carrots like those pictured here be the secret to absorbing more calcium? Two Texas researchers say yes – and they’ve created a carrot they claim allows people to absorb 40% more calcium than normal carrots to back up their claims!

Diabetes-fighting lettuce

lettuce

(Image via FloridaTrend)

Diabetes is one of the most frustrating and life-threatening illnesses out there. Living with it (at minimum) means daily, sometimes painful insulin injections – until now. University of Central Florida professor Henry Daniell has created a genetically modified strain of lettuce (pictured above) that carries the insulin gene. The lettuce cells protect the insulin on its journey through the digestive tract, and when the insulin reaches the intestines, the body’s natural insulin-producing response is triggered.

Lematos

lemato

(Image via FreeWebs)

Okay, so a lemon and a tomato aren’t the most natural of pairs, but that didn’t stop Israeli researchers from bringing us the Lemato! Unlike other genetically altered fruits and veggies (which were created primarily for health reasons), it appears that the lemato was solely an experiment to determine if it was possible to make tomatos give off the scent of lemons. Mission accomplished!

Monday, August 24, 2009

US doctor offers British couples chance to choose sex of child

Jeffrey Steinberg, a US doctor, is offering British couples the chance to choose the sex of their child at his New York clinic.

Dr Steinberg provoked anger earlier this year when he said his fertility clinic could allow parents to produce "designer babies" - choosing eye, hair, skin colour and gender.

Under American law, he is allowed to use pre-implentation genetic diagnosis (PGD) to reveal an embryo's sex. In Britain, it can only be used in screening for genetic diseases.

Half of the embryos undergoing tests in Dr Steinberg's laboratory reportedly belong to British couples while four more will be tested next month.

"Britain is far more conservative than it used to be. They were the innovators but now they've got handcuffs on," Dr Steinberg said.

"From a business standpoint, it's the best thing going. From a medical standpoint, it's a travesty."

America has allowed sex selection - known by its supporters as "family balancing" - since 2001, but US pro-life groups have criticised the destruction of embryos deemed undesirable. Earlier this year, the Pope attacked the "obsessive search for the perfect child" and said a "new mentality is creeping in that tends to justify a different consideration of life and personal dignity".

In Britain, officials have warned parents who go overseas for treatment - often after spotting advertisements on the internet - that they should understand the relevant laws and the impact of the selection on any child who is subsequently born.

Other American medical centres have reported receiving interest from British couples, including the Genetics and IVF Institute in Virginia.

The institute said that up to 15 per cent of the 400 PGD cases it handles a year come from abroad. It said it counsels parents before the procedure.

Gary Harton, its PGD scientific director, told The Times that he tells British patients: "You're no different to any other patient. You're here to get what you want. To get a baby."

Tuesday, August 4, 2009

Science Fail – Freak Pig Shocks Chinese Village

By Jeff Wysaski

piglet-monkey-1

For a species that is universally equated with ugliness, a little piglet born in the small Chinese village of Fengzhang makes Miss Piggy look like Megan Fox.

I’m completely horrified by the photo above, and yet, I…can’t…look…away. As owner Feng Changlin suggests, the little pig’s face – thin lips, bulbous nose, big eyes – looks exactly like a monkey. (Side note: Feng Changlin is a fucking awesome name and should be given to Marvel’s next comic book super villain ASAP.)

Any resemblance to a primate quickly shifts below the neck, however. Though parts of the thing are 100 percent pig, the beast’s back legs are longer than the front legs. Such a disadvantage (advantage?) means the little piglet hops around like a kangaroo.

I don’t know about you, but that fact right there freaks my shit out. I just keep picturing the little thing leaping off the ground and biting my face off.

As expected, the farmer and his wife are completely horrified by the thing. Obviously, they can’t sell the thing because it’s too hideous. And though they want to get rid of it, it appears Feng Changlin’s son won’t let him. Apparently, the young Changlin has taken quite a shine to the little guy. He plays with it and feeds it milk. Is that cute? Or revolting? (Answer: revolting).

Monday, July 20, 2009

How Human Cloning Will Work

Introduction to How Human Cloning Will Work

Cloning Image Gallery

TIME cloning issue
Time & Life Pictures/­Getty Images
Hello, Dolly! After Dolly was cloned in 1997, people worried that humans would be next. See more cloning pictures.

­On July 5, 1997, the most famous sheep in modern history was born. Ian Wilmut and a group of Scottish scientists announced that they had successfully cloned a sheep named Dolly.

If you stood Dolly beside a "naturally" conceived sheep, you wouldn't notice any differences between the two. In fact, to pinpoint the only major distinguishing factor between the two, you'd have to go back to the time of conception because Dolly's embryo developed without the presence of sperm. Instead, Dolly began as a cell from another sheep that was fused via electricity with a donor egg. Just one sheep -- no hanky-panky involved.

While Dolly's birth marked an incredible scientific breakthrough, it also set off questions in the scientific and global community about what -- or who -- might be next to be "duplicated." Cloning sheep and other nonhuman animals seemed more ethically benign to some than potentially cloning people. In response to such concerns in the United States, President Clinton signed a five-year moratorium on federal funding for human cloning the same year of Dolly's arrival [source: Lamb].


­Today, after more than a decade since Dolly, human cloning remains in its infancy. Although cloning technology has improved, the process still has a slim success rate of 1 to 4 percent [source: ­Burton]. That being said, science is headed in that direction -- pending governmental restraints.

Scientists have cloned a variety of animals, including mice, sheep, pigs, cows and dogs. In 2006, scientists cloned the first primate embryos of a rhesus monkey. Then, in early 2­008, the FDA officially deemed milk and meat products from cloned animals and their offspring safe to eat.

But what would human cloning involve, and how could you take sperm out of the reproductive ­equation?

Creating a Human Clone

In January 2001, a small consortium of scientists led by Panayiotis Zavos, a former University of Kentucky professor, and Italian researcher Severino Antinori said that they planned to clone a human in two years [source: Kirby]. At about the same time, news surfaced about an American couple who planned to pay $500,000 to Las Vegas-based company Clonaid for a clone of their deceased infant daughter [source: Clonaid]. Neither venture produced documented success.

cloning
A breakdown of how cloning works.

Then, in 2004, South Korean scientist Hwang Woo-suk announced that he and his research team had cloned 11 human embryos for the purpose of extracting stem cells. However, after reviewing his work, a panel at Seoul National University concluded tha­t his findings were false. There ­hasn't been any confirmed human clone created to date. When discussing cloning in the sense of doing so to make a duplicate of an organism, we refer to it as reproductive cloning

Cloning Corner

­If human reproductive cloning proceeds, the primary method scientists will likely use is somatic ce­ll nuclear transfer (SCNT), which is the same procedure that was used to create Dolly the sheep. Somatic cell nuclear transfer begins when doctors take the egg from a female donor and remove its nucleus, creating an enucleated egg. A cell, which contains DNA, is taken from the person who is being cloned. Then the enucleated egg is fused together with the cloning subject's cell using electricity. This creates an embryo, which is implanted into a surrogate mother through in vitro fertilization.

If the procedure is successful, then the surrogate mother will give birth to a baby that's a clone of the cloning subject at the end of a normal gestation period. As mentioned before, the success rate for this type of procedure is small, working in only one or two out of every 100 embryos. After all, Dolly was the result of 277 previously failed attempts.

­On the surface, human cloning may evoke a similar reaction to the space program's race to the moon -- groundbreaking accomplishment, but what could we actually glean from it? Re-engineering the human reproductive process has made many people nervous that cloning crosses the ethical boundaries of science. But we can't fully evaluate the moral dilemma without first addressing the potential benefits of human cloning.

Cloning Uses

­At the outset of the clone craze, some scientists and companies focused on exploiting the science-fiction aspects of the technology. For instance, Zavos and Antinori, mentioned earlier, aimed to develop cloning to aid infertile couples -- to the tune of approximately $50,000 for the service. The group said that the procedure would involve injecting cells from an infertile male into an egg, which would be inserted into the female's uterus. This child would look the same as his or her father. Then there's the possibility of bringing deceased relatives back to life. A now-defunct company called Genetics Savings & Clone performed this type of cloning for a woman's dead cat, Little Nicky, in 2004.

Cloning on Film

Human reproductive cloning probably won't be a reality any time soon, but you can indulge your curiosity with a few cloning film selections.

  • The Island: Set in 2019, wealthy people keep clones of themselves on an island so if they ever get hurt, they can just snag a body part from their clone by murdering him or her.
  • The Boys from Brazil: If you like Gregory Peck, you may want to steer clear to preserve his old-school, dreamboat image. However, if you like movies about neo-Nazi cloning projects, get the popcorn ready!
  • Multiplicity: Doug Kinney has no time for anything, so he clones himself without telling his family -- let the hilarity ensue.

­Therapeutic cloning holds the most promise of valuable medical advancement. Therapeutic cloning is the process by which a person's DNA is used to grow an embryonic clone. However, instead of inserting this embryo into a surrogate mother, its cells are used to grow stem cells. These stem cells could become the basis for customized human repair kits. They can grow replacement organs, such as hearts, livers and skin. They can also be used to grow neurons to cure those who suffer from Alzheimer's, Parkinson's or Rett syndrome. And since the stem cells would come from embryo clones using your own cell's DNA, your body would readily accept them. For more detailed information on stem cells, you can read How Stem Cells Work.

Here's how therapeutic cloning works:

  • DNA is extracted from a sick person.
  • The DNA is then inserted into an enucleated donor egg.
  • The egg then divides like a typical fertilized egg and forms an embryo.
  • Stem cells are removed from the embryo.
  • Any kind of tissue or organ can be grown from these stem cells to treat various ailments and diseases.

To clone human embryos, however, you need eggs. If therapeutic cloning were to begin in earnest, it could increase the demand for such eggs and potentially create additional moral questions regarding the donors [source: Lamb]. Speaking of ethics, there's plenty of related debate to go around when it comes to human cloning.

Human Cloning Ethics

Surveys have shown that few Americans approve of cloning for reproductive purposes, although more are open to therapeutic cloning [source: Burton]. The U.S. government has established strategic roadblocks related to human cloning, although no federal ban exists. First, the government won't fund research focused on human cloning for reproduction. Also, the FDA, which regulates public cloning research, requires anyone in the United States attempting to clone humans to first get its permission. President George W. Bush's appointed Council on Bioethics unanimously opposed cloning for reproductive purposes.

twins at a table
Symphonie/Getty Images
Human reproductive cloning is banned in more than 50 countries.

Certain countries abroad have stricter standards, and more than 50 have legally banned research efforts on reproductive human cloning [source: Medical Devices & Surgical Technology]. In Japan, human cloning is a crime punishable by up to 10 years in prison. England has allowed cloning human embryos for therapeutic use only. Many individual states have also passed laws restricting cloning.

While legal restrictions are one deterrent to pursuing human cloning at this time, some scientists believe today's technology just isn't ready to be tested on humans. Ian Wilmut, one of Dolly's co-creators, has even said that human cloning projects would be irresponsible. Cloning technology is still in its early stages, and nearly 98 percent of cloning efforts end in failure. The embryos are either not suitable for implanting into the uterus, or die some time during gestation or shortly after birth.

Those clones that do survive suffer from genetic abnormalities. Clone cells may age more rapidly, shortening their lifespan, similar to what happened with Dolly. Some clones have been born with defective hearts, lung problems, diabetes, blood vessel complications and malfunctioning immune systems. One of the more famous cases involved a cloned sheep that was born but suffered from chronic hyperventilation caused by malformed arteries leading to the lungs.

­Opponents of cloning point out that while we can euthanize defective clones of other animals, it's morally problematic if this happens during the human cloning process. Advocates of cloning respond that it's now easier to pick out defective embryos before they're implanted into the mother. In 2005, the United Nations attempted to pass a global ban on human cloning, but was unsuccessful due to disagreements over whether therapeutic cloning should be included. For now, human cloning remains in a stalemate from both a scientific and public policy perspective -- the future of human cloning will likely depend on which side gives in first.

Sources

  • Burton, Kelli Whitlock. "Cloning in America." GeneWatch. November/December 2005.
  • Clonaid Web site.
    http://ww­w.clonaid.com/
  • "Cloning Fact Sheet." Human Genome Project Information. Updated July 23, 2008. (Sept. 3, 2008)
    http://www.ornl.gov/sci/techresources/Human_Genome/elsi/cloning.shtml#policy
  • "Human clones: New U.N. analysis lays out world's choices." Medical Devices & Surgical Technology Week. Dec. 2, 2007.
  • Javitt, Gail H.; Suthers, Kristen; and Hudson Kathy. "Cloning: A Policy Analysis." Genetics & Public Policy Center. May 23, 2005. (Sept. 3, 2008)
    http://www.pewtrusts.org/uploadedFiles/wwwpewtrustsorg/Reports/Genetics_and_Public_Policy/GPPC_Cloning_0505.pdf
  • Kirby, Alex. "Cloned human planned 'by 2003.'" BBC News. Jan. 30, 2001.
    http://news.bbc.co.uk/2/hi/science/nature/1144694.stm
  • Lamb, Gregory M. "How Cloning Stacks Up." Christian Science Monitor. July 13, 2006. (Sept. 3, 2008)
    http://www.csmonitor.com/2006/0713/p13s01-stgn.html
  • "Use of Cloning Technology to Clone a Human Being." FDA. Updated Dec. 27, 2002. (Sept. 3, 2008)
    http://www.fda.gov/CBER/genetherapy/clone.htm

Monday, June 8, 2009

The First GM Human Embryo Could Dramatically Alter the Future

Human_embryo “The advance of genetic engineering makes it quite conceivable that we will begin to design our own evolutionary progress.”

~Isaac Asimov, famous thinker and sci-fi writer

Cornell University researchers in New York revealed that they had produced what is believed to be the world’s first genetically altered human embryo—an ironic twist considering all the criticism the US has heaped on South Korea over the past several years for going “too far” with its genetic research programs. The Cornell team, led by Nikica Zaninovic, used a virus to add a green fluorescent protein gene, to a human embryo left over from an in vitro fertilization procedure. The research was presented at a meeting of the American Society of Reproductive Medicine last year, but details have emerged only after new controversy has emerged over the ethics and science of genetically modifying humans.

Zaninovic has pointed out that in order to be sure that the new gene had been inserted and the embryo had been genetically modified, scientists would ideally want to keep growing the embryo and carry out further tests. However, the Cornell team did not get permission to keep the embryo alive. The GM embryos created could theoretically have become the world’s first genetically altered man or woman, but it was destroyed after five days.

British regulators form the Human Fertilization and Embryology Authority (HFEA), have warned that such controversial experiments cause “large ethical and public interest issues”.

Much of the debate stems from the fact that the effects of genetically altering an embryo would be generational and permanent. In other words, if we create a mutant baby and it grows up to have children of it’s own—they’ll all be mutant gene carriers too. Genes injected into embryos and reproductive cells, such as sperm, affect every cells in the body and would be passed on to future generations. Critics say current humans don’t have the right to tamper with the gene pool of future generations.

On the other hand, proponents of such technology say that this science could potentially erase diseases such as cystic fibrosis, hemophilia and even cancer. In theory, any “good” gene could be added to embryos to offset any “bad” genes they are currently carrying. That could potentially mean the difference between life and death for many children.

John Harris, the Sir David Alliance Professor of Bioethics at Manchester University, takes it a step further. He believes that as parents, citizens, and scientists, we are morally obliged to do whatever we can genetically to make life better and longer for our children and ourselves. Society currently devotes so much energy and resources towards saving lives, which, in reality, is simply postponing death, he notes. If it is right to save life, Harris reasons, then it should also be right to postpone death by stemming the flow of diseases that carry us to the grave.

For Harris, having the ability to improve our species lot in life but refusing to do so, makes little sense. He has a difficult time understanding why some people are so insistent that we shouldn’t try to improve upon human evolution.

“Can you imagine our ape ancestors getting together and saying, ‘this is pretty good, guys. Let’s stop it right here!’. That’s the equivalent of what people say today.”

Ethicists, however, warn that genetically modifying embryos will lead to designer babies preloaded with socially desirable traits involving height, intelligence and coloring.

Dr David King, director of Human Genetics Alert, warns, “This is the first step on the road that will lead to the nightmare of designer babies and a new eugenics.”

Harris, however, doesn’t support that argument. He says it’s not about “beauty” it’s about health, and what parent wouldn’t want a healthy child, he asks.

“Certainly, sometimes we want competitive advantage [for our children], but for the enhancements I talk about, the competitive advantage is not the prime motive. I didn’t give my son a good diet in the hope that others eat a bad diet and die prematurely. I’m happy if everyone has a good diet. The moral imperative should be that enhancements are generally available because they are good for everyone.”

The only other route to equality, he says, is to level down so that everyone is as uneducated, unhealthy and unenhanced as the lowest in society – which would be much more unethical in his opinion. Even though we can’t offer a liver transplant to all who need them, he says, we still carry them out for the lucky few. “Much better to try to raise the baseline, even if some are left behind.”

The Human Fertilization and Embryology Bill in currently under consideration in Britain will likely make it legal to create GM embryos in that country, but only for research—implantation in the womb will still be banned—at least for now. However, ethicists believe that the legislation could easily be relaxed even further in the future.

People who believe that genetically modified humans is something way into the future might want to consider that many experts are worried that some forms of it are already happening in the sports world.

Faster, bigger, better, stronger—in theory, the single most effective way to radically alter your physical capacities is to manipulate your genes. Athletes are beginning to take notice. Now that we’ve mapped out the human genome and identified exactly which genes make you buff, tough and rough—experts are concerned about the future of genetic doping.

Gene doping could spawn athletes capable of out-running, out-jumping and out-cycling even the world’s greatest champions. However, researchers at the University of Florida are attempting to prevent that from happening by detecting the first cases of gene doping in professional athletes before the practice becomes mainstream.

Montreal-based World Anti-Doping Agency (WADA), responsible for monitoring the conduct of athletes, is working with investigators around the globe to develop testing to identify competitors who have injected themselves with genetic material that is capable of enhancing muscle mass or heightening endurance.

“If an athlete injects himself in the muscle with DNA, would we be able to detect that?” asked one of France’s leading gene therapy researchers, Philippe Moullier, M.D., Ph.D., director of the Gene Therapy Laboratory at the Universite de Nantes in France.

Right now, he says the answer is clearly “no”. But that may soon change. The UF scientists are among several groups collaborating with national and global anti-doping organizations to develop a test that can detect evidence of “doped” DNA.

“WADA has had a research program in place for some years now, to try to develop tests for gene-based doping,” said Theodore Friedmann, M.D., head of the agency’s panel on genetic doping and director of the gene therapy program at the University of California, San Diego.

Nearly every day now we are inundated with new genetic discoveries. Scientists can now pinpoint many specific genes including being lean, living a long life, improved self-healing, thrill seeking behavior, and having an improved memory among many other incredible traits. Many believe that these genes can be manipulated in ordinary humans, in effect creating Super-Mutants.

Theoretically, options are nearly limitless. Even a gene that exists in another species could be brought over to a human cell. Imagine some of the incredible traits of the animal kingdom that some humans don’t possess such as night vision, amazing agility, or the ability to breath underwater. The precedence for these types of radical changes is already in place. Experimental mice, for example, were successfully given the human ability to see in color. If animals can be engineered to have human traits, then humans can certainly be mutated to have desirable animal traits.

It is even thought possible to so drastically alter human genomes that a type of superhuman species could emerge. The fear with germline engineering is that since it is inheritable, offspring and all succeeding generations would carry the modified traits. This is one reason why this type of engineering is currently banned- it could lead to irreversible alteration of the entire human species.

Ethics, not scientific limitations, is the real brick wall. Most scientists believe manipulating genes in order to make an individual healthy is a noble and worthwhile pursuit. Some are against even that notion, arguing that historically amazing individuals have sometimes been plagued by genetic mental and physical disorders, which inadvertently shaped the greatness of their lives. Should we rob the human race of character shaping frailty? Very few scientists would dare to publicly endorse the idea of using genetic engineering to make a normal, healthy individuals somehow superior to the rest of the human race.

“The push to redesign human beings, animals and plants to meet the commercial goals of a limited number of individuals is fundamentally at odds with the principle of respect for nature,”
said Brent Blackwelder, President of Friends of the Earth in his testimony before the Senate Appropriations Committee.

However, would it be so bad if the human race were slightly improved? What if a relatively simple procedure could make an individual and his or her offspring resistant to cancer? After all, Nature isn’t always right. Nature has naturally selected many people to carry the burden of uncomfortable and often lethal genetic disorders. If nature knows best, then shouldn’t we quit trying to “improve” upon nature by “curing” people of genetic conditions we consider inferior? Many say we shouldn’t change human genetics, UNLESS it’s the RIGHT thing to do. Who gets to decide where the line is between righteous endeavor and the corruption of nature? These are the questions facing our generation.

Posted by Rebecca Sato

Thursday, May 28, 2009

Glowing Monkeys Make More Glowing Monkeys the Old-Fashioned Way

monkey_1

The first genetically modified primates that can pass their modifications to their offpsring have been created by Japanese scientists.

The marmosets, pictured above, express a green fluorescent protein in their skin. The gene for producing the glow was delivered to the first marmoset embryos via a modified virus. But now that modification method could become unnecessary. One male marmoset, number 666, fathered a child (pictured at right) that also contained the transgenes.

“The birth of this transgenic marmoset baby is undoubtedly a milestone,” developmental biologists Gerald Schatten and Shoukhrat Mitalipov at the Pittsburgh Development Center and Oregon Stem Cell Center, respectively wrote in a commentary accompanying the study Thursday in Nature. “The cumbersome and often frustrating process of making a transgenic animal from scratch need now only occur with founder animals.”

monkey_2Transgenic animals are a key tool in the biomedical researchers’ toolbox. They allow scientists to model the function of genes and the efficacy of treatments. Many transgenic mice lines exist, but often the small rodents are too different from humans to effectively extrapolate their responses to human beings. Primates, on the other hand, are far closer biologically to humans, but before the new technique, creating primate models had proven difficult and expensive.

Now, biologists may be able to produce whole groups of marmosets that mimic humans with genetic diseases like cystic fibrosis.

“Subsequent generations can be produced by natural propagation, with the eventual establishment of transgene-specific monkey colonies — a potentially invaluable resource for studying incurable human disorders, and one that may also contribute to preserving endangered primate species,” Schatten and Shoukhrat continued.

Instead of using bonobos or chimps, the research team led by Erika Sasaki at the Central Institute for Experimental Animals in Japan picked the common marmoset because its “size, availability, and unique biological characteristics” make it a potentially useful animal, particularly in tough fields like neuroscience and stem cell research.

Thursday, April 23, 2009

Fertility expert: 'I can clone a human being'

Controversial doctor filmed creating embryos before injecting them into wombs of women wanting cloned babies

By Steve Connor, Science Editor


Cady, died aged 10 in a car crash in the US. Her blood cells were frozen and sent to Dr Zavos, who fused them with cow eggs to create cloned human animal hybrid embryos

Cady, died aged 10 in a car crash in the US. Her blood cells were frozen and sent to Dr Zavos, who fused them with cow eggs to create cloned human animal hybrid embryos

    Tuesday, April 21, 2009

    World's first cloned camel unveiled in Dubai

    The ambitious desert emirate of Dubai has claimed another first, this time in the science of cloning camels.

    By Richard Spencer in Dubai
    Injaz camel: Dubai claims world's first cloned camel
    Injaz, claimed to be the world's first cloned camel. Injaz, a female, was born on April 8, 2009 Photo: AFP

    Injaz, or Achievement, was unveiled to the world alongside her surrogate mother five days after being born at the city's Camel Reproduction Centre.

    "This is the first time scientists have cloned a camel calf," the scientific director of the central veterinary research laboratory, Dr Ulrich Wernery, said. "She is a healthy female."

    The project had the personal backing of Dubai's ruler, Sheikh Mohammed bin Rashid al-Maktoum, best known in Britain as one of the world's leading racehorse owners.

    The Camel Reproduction Centre now hopes to use the technique on some of Dubai's leading racing camels to preserve elite bloodlines for the future.

    Camel racing is a popular past-time in the Gulf region, though the traditional child riders have largely been replaced by robots due to humanitarian concerns.

    "We are all very excited by the birth of Injaz," Dr Lulu Skidmore, the centre's scientific director, said. "This significant breakthrough in our research programme gives a means of preserving the valuable genetics of our elite racing and milk-producing camels in the future."

    The scientists employed the standard animal cloning techniques first used in the case of Dolly the sheep in 1996 by scientists in Edinburgh.

    Injaz is the clone of a camel slaughtered for its meat in 2005. The ovaries were removed and DNA extracted and placed in an egg taken from and re-implanted into the surrogate mother.

    Tests since Injaz's birth have shown the camel's DNA to be a copy of the dead animal, not the mother.

    The birth, after an "uncomplicated" gestation period of 378 days, followed a number of unsuccessful attempts at producing a clone.

    The Camel Reproduction Centre previously produced the world's first "Cama", the first surviving hybrid of a camel and a guanaco, a type of llama.

    Friday, April 3, 2009

    Crazy genetics: Can chickens turn back into dinosaurs?



    fora.tv — A look back at our own history, and a question about creating a really tiny dinosaur. Do you think this could be possible?

    Friday, March 6, 2009

    Baby Olympian? DNA test screens sports ability

    MSN Tracking Image
    MSNBC.com


    Duane Hofmann / msnbc.com


    But some worry about mental toll the results of at-home test may bring
    By Bill Briggs
    msnbc.com contributor
    updated 9:04 a.m. ET, Wed., March. 4, 2009

    Ava Anderson can’t run — not yet anyway. And the only iron she pumps comes via her tiny spoon. Then again, she’s just 13 months old.

    But Ava was born with a genetic blend that will infuse her body with the explosive bursts of a power athlete and the steady engine of marathoner. Someday, this baby may blossom into a multisport, cross-training double threat. That’s not parental conjecture. That’s her DNA profile.

    Her mom and dad had her tested.

    Like more than 200 other parents to date, Hilary and Aaron Anderson paid $149 to Atlas Sports Genetics — a Boulder, Colo. company — for a sneak peek at their kid’s athletic horizons.

    The Andersons received a home-analysis kit to check whether Ava has the inborn knack for strength sports (like sprinting) or endurance sports (like cycling). Then, to get the genetic scoop, they simply brushed the inside of Ava’s cheek with two cotton swabs, sealed the samples in a baggie and mailed them to an Australian lab used by Atlas. Although there are 20,000 strands of human DNA, the lab hunts for variations of just one: ACTN3, which can predict certain athletic skills, some experts believe. Five weeks later, the Andersons heard the verdict.

    “She’s a mix,” said Hilary Anderson, who wasn’t surprised by the results given that she is tall and lean and that her husband once trained for the U.S. Olympic weightlifting team. “If she came back all endurance, we’d probably focus more on the long-distance type things. Likewise, if she was all strength, we would direct her toward power sports. This will let her try all sorts of things.”

    Added pressure?
    But the Andersons also understand one more thing about the test: It is drawing fire from scattered coaches, therapists and genetic experts who worry some parents will misuse the data and that the young science will inject even more pressure and politics into childhood games.

    “It is simply dangerous,” said Casey Cooper, a sports psychologist who hosts a radio show on KLAA-830 AM in Anaheim, Calif., and mother of a 5-year-old. “The more we professionalize sports younger and younger, the more we contribute to the youth drop-out rate for sports. My reaction: Save your money because to (genetically) type your child like this is only going to land them in my office later. And I charge $150 [per session].”

    At the same time, some coaches say locker-room chemistry could be shattered if roster cuts or playing time are influenced by the knowledge that one player is genetically gifted — or not.

    “Wow, I just think you’re opening a Pandora’s Box with team dynamics,” said Chad Onken, an assistant coach of the swim team at the YMCA of the Triangle in Raleigh, N.C. The youthful squad has won six national titles. “You’re talking about a small problem that could blow up to something pretty huge. “

    Still, the Andersons know all about the possible parental pitfalls. They have seen overbearing, overexpectant moms and dads up close. (The couple ran strength and conditioning camps for kids a few years back.) Consequently, they are sensitive to those emotional snares, they say.

    “So many parents thought their kid was going to be the next Bo Jackson (a former pro football and baseball star). There are going to be those parents, unfortunately, who push their kids, who live through their kids,” said Hilary, a personal trainer who played college volleyball. “For us, this was just a little side thing to help make it be fun. If Ava would rather do music or dance, that’s fine.”

    Atlas president and co-owner Kevin Reilly acknowledges being uneasy about clients who receive DNA results that dampen the sports dreams they hold for their kids — for example, if they learn their little boy is not genetically apt to excel at a power sport such as football.

    “I think this may be a gut check for parents to look at their motives as well: What’s in the best interest for my child, (to ask themselves) what do I want them to be and what do they want to be,” Reilly said.

    What’s more, the test can’t predict a future NFL star, Reilly said. It merely reveals if a child has the genetic markers common to people who succeed in either power or endurance events. In short, Reilly is selling the product as a parental “tool,” a DNA roadmap, a device to eventually expose children to the sports they were born to play.

    The sports-DNA test has one gaping blind spot as well, YMCA coach Onken said. It can’t measure an athlete’s desire, while natural talent doesn’t always translate into a winner. The YMCA of the Triangle, which includes 350 kids from ages 7 to 18, has produced Olympic hopefuls and college-scholarship swimmers. Some of those, Onken said, excelled purely on heart and hard work. He compared them to the tiny-but-driven Notre Dame football player profiled in the 1993 movie “Rudy.”

    “I can think of too many ‘Rudy’ types who overachieved here,” Onken said. “And I can think of too many playground basketball legends who could jump over a backboard but never made it off the playground.”

    Science in question
    The science, however, has doubters.

    This much is known: We all have the ACTN3 gene; we get one copy from each parent. As with many genes, though, ACTN3 can take different twists. One version of the gene — the R variant — steers the body to produce a protein that builds more fast-twitch muscles, used for potent surges of energy. The X variant, meanwhile, blocks that protein. People who inherit two sets of the R variant may be naturally engineered for power sports. Those who carry two X variant copies may have better stamina.

    The “mixed pattern” people — like Ava Anderson — “may be equally suited for both endurance and sprint/power events,” says the Atlas Web site.

    But Carl Foster, who co-authored an ACTN3 study and who heads the human performance lab at the University of Wisconsin-La Crosse, points out that multiple genes fuel athleticism, and scientists are just beginning to learn which are most vital.

    “So why do you want to spend money looking for one gene?” Foster asked. “You want parents to be supportive of their kids’ endeavors. You don’t want them to try and program their kid. And the kinds of people with disposable income are probably the kinds of people where that’s always a trap for them. They’re accomplishment-oriented.

    “They say, ‘Well, I want my kid to be the best he can be.’ Of course. It’s God, mother and apple pie. You can’t vote against it. But at some point you’d like to say: Maybe just go to the Y and put your kid in a sports class and just see if they like it.”

    Chemists Building "Organs From Scratch"

    Scientists say they expect that eventually, clusters of cells could be built on clusters to make artificial organs that someday may be implanted into humans.

    Synthetic biologists are getting closer to creating man-made organs made out of genetically engineered cells.

    Two Cal chemists announced Tuesday they have assembled different types of genetically engineered cells into synthetic microtissues that can perform functions such as secreting and responding to hormones.

    They said that means more complex biological capabilities, like the kinds done by a liver or a heart or a kidney, are not out of the question at some point soon.

    "While the synthetic tissues today comprise only a handful of cells, they could eventually be scaled up to make artificial organs," the university media office said in a statement. "Those could help scientists understand the interactions among cells in the body and might some day substitute for human organs."

    "People used to think of the cell as the fundamental unit. But the truth is that there are collections of cells that can do things that no individual cell could ever be programmed to do. We are trying to achieve the properties of organs now, though not yet organisms," "This is like another level of hierarchical complexity for synthetic biology," said coauthor Carolyn Bertozzi, UC Berkeley professor of chemistry and of molecular and cell biology. She is also the director of the Molecular Foundry at Lawrence Berkeley National Laboratory.

    "As synthetic biologists cram more and more genes into microbes to make genetically engineered organisms produce ever more complex drugs and chemicals, two University of California chemists have gone a step further," the university media office said.

    "We are really taking this into the third dimension now, which for me is particularly exciting," said first author Zev J. Gartner, a former UC Berkeley post-doctoral fellow. "We are not simply linking cells together, we are linking them together in 3-D arrangements, which introduces a whole new level of cellular behavior which you would never see in 2-D environments."

    The Hope: Build Organs "From Scratch"

    Gartner and Bertozzi report on their assembly of three-dimensional microtissues this week in the online early edition of the journal Proceedings of the National Academy of Sciences.

    One type of cell that needs other cells to make it work properly is the stem cell, Bertozzi said

    Theoretically, using Gartner and Bertozzi's chemical technique, it should be possible to assemble stem cells with their helper cells into a functioning tissue that would make stem cells easier to study outside the body.

    "In principal, we might be able to build a stem cell niche from scratch using our techniques, and then study those very well defined structures in controlled environments," Bertozzi said.

    Bertozzi said that most of the body's organs are a collection of many cell types that need to be in actual physical contact to operate properly.

    The pancreas, for example, is a collection of specialized cells, including insulin-secreting beta cells, that "sense glucose from the environment and respond by producing insulin. A complex feedback regulatory loop goes into all of this, and you need more than one cell type to achieve such regulation."

    "If you really want to understand the way these cells behave in an organism, especially a human, you would like to recapitulate that environment as closely as possible in vitro," Gartner said. "We are trying to do that, with the aim that the rules we learn may help us control them better."

    How They Did It…

    Gartner and Bertozzi assembled three types of cultured cells into onion-like layers by using two established technologies: DNA hybridization and Staudinger chemistry.

    DNA hybridization is like a "programmable glue," she said, that can stick cells together because of the highly precise nature of binding between complementary DNA strands: One strand of the DNA helix binds only to its complementary strand and nothing else. By putting a short DNA strand on the surface of one cell and its complementary strand on another cell, the researchers assure that the two lock together exclusively.

    To get these specific DNA strands onto the cells, they used chemical reactions that do not interfere with cellular chemistry but nevertheless stick desired chemicals onto the cell surface.

    The technique for adding unusual but benign chemicals to cells was developed by Bertozzi more than a decade ago based on a chemical reaction called the Staudinger ligation.

    After proving that they could assemble cells into microtissues, Gartner and Bertozzi constructed a minute gland - analogous to a lymph node, for example - such that one cell type secreted interleukin-3 and thereby kept a second cell type alive.

    "What we did is build a little miniaturized, stripped-down system that operates on the same principle and looks like a miniaturized lymph node, an arrangement where two cells communicate with each another and one requires a signal from the other," she said. "The critical thing is that the two cells have to have a cell junction. If you just mix the cells randomly without connection, the system doesn't have the same properties."

    She expects that eventually, clusters could be built on clusters to make artificial organs that someday may be implanted into humans.

    "Our method allows the assembly of multicellular structures from the bottom up. In other words, we can control the neighbors of each individual cell in a mixed population," she said. "By this method, it may be possible to assemble tissues with more sophisticated properties."

    One aspect of the technique is that DNA hybridization seems to be temporary, like a suture. Eventually, the cells may substitute their own cell-cell adhesion molecules for the DNA, creating a well-knit and seemingly normal, biological system.

    The research was funded by the U.S. Department of Energy as well as the Howard Hughes Medical Institute.