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Dead embryos can be used to make new stem cells

James Randerson, science correspondent
Thursday September 21, 2006
Guardian Unlimited

Scientists have created embryonic stem cells using dead embryos, it was
revealed today. By avoiding the need to deliberately destroy an embryo, the
technique could offer a way of producing embryonic stem cell lines that
would be ethically acceptable to pro-life groups.
Embryonic stem cells are capable of turning into any cell or tissue type in
the body, and scientists think they offer great potential to treat diseases
such as Alzheimer's. But to create a stem cell line scientists have had to
destroy an embryo - typically one that is surplus to requirements during IVF
treatment.
Now Miodrag Stojkovic at Sintocell in Leskovac, Serbia and his team has
shown that it is possible to establish stem cell lines from embryos that
have stopped dividing. Some embryos are not implanted during IVF treatment
because they have visible defects. The new findings suggest that these could
be used to make stem cells lines.
"My purpose was to demonstrate in a scientific manner that these arrested
embryos - dead embryos - could be used for scientific purposes," said Dr
Stojkovic, who was part of the British team that cloned the first human
embryo in 2005. He said he supports the use of living embryos to harvest
stem cells, but added that using dead embryos might allow scientists to
circumvent restrictions, in countries such as the United States, on using
live embryos to create stem cells.
The study, which is published in the journal Stem Cell, used very early
embryos that are bundles of between 4 and 24 cells. Out of 13 embryos that
stopped dividing at 6 to 7 days old, cells extracted from 5 of these went on
to develop structures typical of stem cells. The scientists were able to
establish a stem cell line from one of these. By comparison, using living
4-day-old embryos, the team was able to establish 2 new stem cell lines.
However, Helen Watt, director of the catholic Linacre Centre for Healthcare
Ethics said ethical concerns remained. "If the aim in waiting for natural
death - or what we guess is natural death - is to satisfy legal or political
concerns, the death of these embryos may even be intended, not merely
foreseen," she said.
Dr Watt added that the Catholic church had "serious moral concerns" about
IVF anyway. "Use of IVF embryos - even dead embryos - would normally involve
close complicity with IVF practitioners, of a kind which could not be
justified."
Robin Lovell-Badge, a leading stem cell scientist at the National Institute
for Medical Research in London, said the researchers could not be sure that
an embryo was truly dead.
"They have no proof that this embryo, if it had been transferred back into a
womb perhaps a day or two days earlier, would not have produced a baby," he
said, "You can never answer that question."
The problem, he said, is that conditions in the lab can never be as
favorable as they would be in the womb, so an embryo that could have
survived there might appear inviable in the petri dish. "The culture
conditions are never perfect, and just by slightly mishandling an embryo you
can compromise its ability to develop."
But Robert Lanza, a stem cell expert at Advanced Cell Technology in
Worcester, Massachusetts, welcomed the study. "We need to pursue all the
options open to us," he said. "The question is whether we will be able to
convince the politicians that it makes any difference."
In a separate study published in Cloning and Stem Cells, Dr Lanza's team
showed that it is possible to repair eye disease in rats using human
embryonic stem cells. The rats he used had damage similar to age-related
macular degeneration, a disease that afflicts 30 million people worldwide,
typically those over 60. The study involved injecting stem cells into the
space below the retina.

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