Stem Cell.
Publié le 11/05/2013
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The medical profession used adult stem cells to treat diseases long before anyone isolated one.
In 1968 scientists performed the first successful bone marrowtransplant, a procedure in which a patient receives an infusion of healthy bone marrow cells.
The purpose of such transplants is to restore the blood-making capabilitiesof the patient’s diseased bone marrow after extremely strong chemotherapy has destroyed that bone marrow.
From the beginning investigators suspected that stemcells in the infused bone marrow make this technique work.
Bone marrow transplants are now a standard therapy for certain cancers, such as leukemia and lymphoma,and for other diseases of the blood and bone.
Other stem cell therapies in current use involve blood stem cells isolated from drawn blood and taken from umbilicalcords.
See also Medical Transplantation.
By the beginning of the 21st century researchers had not yet developed any medical treatment that relied on isolated stem cells grown in culture.
Because of theirability to repair tissue damage, stem cells could serve as starting points in therapy for a wide variety of medical conditions, including Alzheimer’s disease, whichdamages brain cells, especially those related to memory, and Parkinson disease, which damages nerves that control the muscles.
Other diseases, such as diabetes,heart disease, and leukemia, might also be treated with stem cells to replace or repair damaged, diseased, or lost cells and tissues.
VI THE GOVERNMENT AND STEM CELL RESEARCH
After the isolation of stem cells, the controversy that developed over their use soon involved the United States government, which funds much of the country’s medicalresearch.
In November 1998 President Bill Clinton asked the National Bioethics Advisory Commission, an advisory committee appointed by the president, to investigatethe medical and ethical issues behind stem cell research.
That commission encouraged federal funding for research on embryonic stem cells, as long as these cells camefrom the tissue of dead fetuses or from embryos that remained after infertility treatments.
Yet differing opinions prevented a firm government commitment to fundingresearch in this field.
In August 2001 President George W.
Bush announced a new government position: Federal funding would be available for stem cell research, but only for research onexisting stem cell lines.
In other words, stem cells already in culture could be used in federally funded projects, but scientists could not isolate additional sources of stemcells.
Researchers can choose to adhere to these guidelines or rely on private funding.
The head of Bush’s Council on Bioethics has said embryonic cloning is morally wrong because embryos are destroyed in the process of extracting stem cells, womencould be exploited as egg donors, and the techniques could lead to cloning human beings.
In 2006 Bush vetoed a bill to allow increased federal funding for research onembryos that had been discarded by fertility clinics.
The bill had already been passed by Congress.
Current U.S.
government policy equates the destruction of anembryo with the destruction of a human life and prohibits federal funding for such research.
In addition, a number of states forbid embryonic stem cell research, andsome ban cloning for any purpose.
Researchers are seeking new techniques for harvesting stem cells without harming the embryo, thus avoiding the ethical issues that have blocked stem cell research.
In2006 Massachusetts researchers at the Worcester, Massachusetts, laboratory of Advanced Cell Technology, Inc., announced a technique for extracting a single cell(blastomere) from a two-day-old embryo that consists of eight cells.
The extracted blastomere cell is then grown in the laboratory to start a stem cell line.
The sampledembryo itself is unharmed.
In early 2007 researchers in North Carolina reported success in harvesting stem cells from amniotic fluid, the liquid that surrounds a fetus inthe womb.
The cells can be captured during amniocentesis tests given to pregnant women.
More research is needed to confirm the effectiveness of both techniques.
Other researchers have used cloning techniques to insert the nucleus from a skin cell from one individual into a human egg that has had its own nucleus with DNAremoved.
The egg began to develop into a blastocyst with DNA matched to the new individual’s immune system.
The egg did not develop to the stage of producingembryonic stem cells, but this step may be reached in the future.
However, using a human egg carries similar ethical issues to using embryos, in the views of somepeople.
An important advance in the study of stem cells has been the genetic reprogramming of ordinary differentiated cells to act like embryonic stem cells.
In work firstannounced in 2007, viruses were used to insert genetic instructions into human skin cells that made the cells pluripotent (able to make all other types of cells), similarto embryonic stem cells.
However, using viruses carries the risk of tumors or cancer, and other, safer methods of reprogramming cells will need to be developed.
It isnot yet known if such induced pluripotent stem cells are truly equivalent to embryonic stem cells.
Using a patient’s own cells to create the reprogrammed equivalents ofstem cells would avoid problems with immune system rejection, however.
Because such techniques do not require human embryos or human eggs, research andtherapies with reprogrammed cells could also avoid possible ethical objections and legal restraints.
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