October
2, 2006
Scientists Report Advances in Stem Cell Technology
Two groups of researchers, one in
the United States and the other in
Japan, recently announced progress
in stem cell technology that could
have implications for future applications
of stem cells to disease treatment.
Embryonic stem cells have been proposed
as a way to treat neurodegenerative
diseases, such as amyotrophic
lateral sclerosis (ALS), because
they’re presumably capable of
becoming various kinds of cells in
the nervous system.
To treat muscle diseases, most researchers
favor using cells that are a little
further along in their development
toward muscle than embryonic stem
cells are. (Stem cells derived from
people with genetic disorders, researchers
caution, have the same genetic flaw
that caused the disease originally
and, therefore, have to be genetically
altered before they can be used as
therapy.)
Irina Klimanskaya and colleagues
at Advanced Cell Technology, a private
biotechnology company in Worcester,
Mass., announced online Aug. 23 in
the journal Nature that they had created
embryonic stem cells from embryo “biopsies,”
a technique that theoretically should
leave the original embryo intact.
Embryo biopsies, which are already
in use to diagnose genetic abnormalities
in embryos before they’re implanted
in a woman’s uterus, take a
single cell from an embryo at a stage
when all the cells in the embryo are
alike, usually at the eight- to 10-cell
development stage.
Until now, deriving a new line of
human embryonic stem cells has required
destruction of the embryo, to which
many people are opposed.
In another development, Kazutoshi
Takahashi at Kyoto (Japan) University
and Shinya Yamanaka at the Japan Science
and Technology Agency in Kawaguchi
announced in the Aug. 25 issue of
the journal Cell that they’ve
succeeded in deriving cells that behave
much like embryonic stem cells from
mouse skin cells.
Reasoning that the difference between
a cell that’s “pluripotent,”
or able to mature into a variety of
cell types, and one that isn’t,
is based on the presence or absence
of certain genes, they selected 24
candidate genes that carry instructions
for proteins that induce pluripotency.
They narrowed the necessary genes
and proteins down to four, which they
say can turn skin cells into “induced
pluripotent stem cells” if grown
under the right laboratory conditions.
They caution that they don’t
know whether the technique is applicable
to humans, but they say “the
finding is an important step in controlling
pluripotency, which may eventually
allow the creation of pluripotent
cells directly from somatic [not sperm
or egg] cells of patients.”
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