2 embryonic stem-cell techniques might offer compromise

October 17, 2005|By KAREN KAPLAN | KAREN KAPLAN,LOS ANGELES TIMES

Scientists say they have created viable embryonic stem-cell lines without destroying any embryos - a development that could clear ethical barriers that have sharply restricted federal funding for the controversial research.

Two techniques were demonstrated in mice, and researchers are optimistic the processes could be replicated with human cells. The new methods were published online yesterday by the journal Nature.

Scientists and ethicists said the approaches offer a potential compromise with social conservatives who see embryonic stem-cell research as an untenable trade-off that amounts to destroying life to create medical cures.

Dr. William Hurlbut, an influential member of the President's Council on Bioethics, said he has convinced several religious and conservative philosophers that at least one of the new approaches is morally sound.

But given the intractable debate about when life begins, there are lingering ethical concerns.

Neither method "really quells the ethical debate," said Dr. George Daley, a professor of biological chemistry and molecular pharmacology at Harvard Medical School. "It's not clear it's going to answer all the critics."

Protection of human embryos has been the guiding principle behind President Bush's stem-cell funding policy.

Bush was the first to approve federal funds for the research, but he limited the money to about 20 usable cell lines in existence in 2001 to avoid having taxpayers subsidize the destruction of embryos.

Those lines, which have proved unsuitable for some research, were derived from frozen embryos donated by couples who no longer needed them for in vitro fertilization.

The federal restrictions have hampered scientists seeking to tap the therapeutic potential of embryonic stem cells, which have the apparent ability to grow into any cell type in the human body.

Researchers believe, for example, that the cells eventually might be used to treat juvenile diabetes by growing replacements for faulty islet cells that make insulin.

Some researchers have moved forward by using private funds to create their own lines of embryonic stem cells.

One of the new approaches is based on a routine procedure used by fertility clinics to look for genetic defects in embryos.

Dr. Robert Lanza, medical director for Worcester, Mass.-based Advanced Cell Technology Inc. and an author of one of the papers, extracted a single cell from a mouse embryo that had developed in the laboratory into an eight-cell bundle.

After removing the cell, called a blastomere, Lanza's team surrounded it with embryonic stem cells from the Bush-approved lines, enabling it to pick up the appropriate biochemical cues to start behaving like one of them.

Using 125 blastomeres, they were able to create five cell lines that tests found had the same properties as embryonic stem cells.

When the seven-cell embryos were implanted into surrogate mothers, they resulted in live births 49 percent of the time, virtually the same as for regular eight-cell embryos.

Human stem-cell lines could be created using single cells extracted for genetic diagnosis at in vitro fertilization clinics, Lanza said.

In a laboratory dish, the extracted cell would be allowed to divide into two. One cell could be screened for genetic defects and the other used to create stem cells, he said.

"It's relatively simple, it does not damage the embryo, and it's been used on thousands of healthy babies," Lanza said.

The other approach, developed by Massachusetts Institute of Technology biologist Dr. Rudolph Jaenisch, relies on deactivating a gene needed to implant an embryo into a uterus.

Jaenisch altered mouse DNA and inserted it into an egg whose own DNA had been removed using a common stem-cell procedure called nuclear transfer.

Because the resulting embryo could not attach to the uterus, it would have no chance to develop into a healthy baby, thus avoiding any ethical quandary. Hurlbut, the presidential adviser, strongly backs this approach.

After the DNA insertion, the egg was prompted to begin developing and stem cells were harvested a few days later.

To complete the experiment, the researchers turned the silenced gene back on. The resulting stem cells demonstrated the same abilities as traditional embryonic stem cells.

Karen Kaplan writes for the Los Angeles Times

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