http://news.independent.co.uk/world/science_technology/article311555.ece

Embryos created by 'virgin conception' 
By Steve Connor, Science Editor 
Published: 10 September 2005 
Scientists have created the first human embryos in Britain by a technique of 
"virgin conception" that does not involve either fertilisation with sperm or 
cloning. The six embryos lived for between three and five days and were created 
as a potential source of human stem cells, which can develop into the body's 
specialised tissues such as brain nerves or bone. 

Each embryo came about as a result of parthenogenesis, when an egg divides 
without being fertilised into a ball of cells that develops in effect into an 
early embryo called a blastocyst.

Paul de Souza, the study's principal investigator at the Roslin Institute in 
Edinburgh, said that although the aim was to harvest stem cells from the 
embryos, efforts to do this had so far not been successful. "We've made half a 
dozen blastocysts. We have not at present got embryonic stem cells, that 
continues to be our ambition," Dr de Souza told the British Association for the 
Advancement of Science meeting in Dublin.

Parthenogenesis - which literally means virgin birth - is a common form of 
asexual reproduction in many animals but not in mammals, the group to which 
humans belong.

Dr de Souza said there was no intention of implanting the embryos into the womb 
of a woman and that his government licence from the Human Fertilisation and 
Embryology Authority was strictly for research. "If we don't put these 
artificial conceptuses into a uterus, they will go nowhere. They will not 
result in a foetus, they will not result in a life," he said.

The announcement of the first human embryos created by parthenogenesis is 
likely to be criticised by "pro-life" groups who oppose all research that 
involves creating human embryos for research purposes, he said.

The scientists at the Roslin Institute, where Dolly the sheep was cloned, used 
about 300 eggs taken from the ovaries of women undergoing an operation to make 
them sterile who had given their consent. About half the eggs matured 
successfully in the laboratory and about 5 per cent of these divided several 
times to produce a blastocyst, he said.

"We need a blastocyst to recover embryo stem cells and our success rate in 
recovering embryo stem cells is about one in ten," Dr de Souza said. "I think 
it's more of a technical challenge [to get stem cells] as distinct from a 
biological challenge."

Normally eggs and sperm have only half the genetic material and chromosomes of 
other cells in the body but the scientists have developed a technique whereby 
the eggs are stimulated to retain all their chromosomes before developing into 
a pathenogenic embryo.

"We can manipulate that process where normally genetic information is expelled, 
so that we can create eggs and embryos whose genetic constitution is identical 
to the mother," Dr de Souza said.

"The tissue we can derive from such an embryo would presumably be compatible 
for transplantation.

"There are in existence parthenogenic stem cell lines from non-human primates 
but to date no one has cracked that in humans. I think it's just a matter of 
the supply of tissue with which to be able to engage in experimentation," he 
added.

At present only women could benefit from parthenogenic embryos as men cannot 
produce eggs but scientists are also working on the possibility of using 
genetic material from sperm to create a parthenogenic embryo.

"Based on experiments in mice we could create what are called androgenotes 
where we would replace the egg's genetic information with the genetic 
information from a sperm," Dr de Souza said.

"We could put in two sperms if we wanted to to create a full genetic 
complement. Androgenotes would be a little more problematic in terms of how 
exactly matched that tissue would be to the donor because those sperm could 
have been created through a process where there would have been an expulsion of 
genetic material," Dr de Souza said.

Parthenogenic embryos offer an alternative way of creating stem cells than 
cloned embryos, which are created by transfering the nucleus of a skin cell 
into an egg with its own nucleus removed. Dr de Souza said: "It is possible 
that the cloned stem cell lines that are produced will not be suitable for 
therapeutic purposes or not suitable for use as models of genetic diseases.

"We don't know whether any one of them is going to lead to where to want to go 
and therapy is not the only objective. We also want these cell lines for 
research," he added. 


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