 Under President Bush researchers were banned from using new stem cell lines for federally funded research. President Obama has now lifted that ban, allowing 13 new stem cell lines to be applicable for potentially life-saving federally funded research.
 Embryonic stem cells can be put to use developing treatments for diseases such as Parkinson's, sickle cell anemia, diabetes, and spinal cord injuries. (Source: University of Wisconsin)
Researchers now have access to 13 new lines of stem cells, opening a wealth of possibilities
Embryonic stem cell lines promise to
unlock incredible new therapies, allowing tissue types to be regrown
and diseases such as Parkinson's disease, sickle
cell anemia, and spinal
cord injuries/defects to be truly treated for the first time.
However, a moral debate long limited these potentially life-saving
research tools. Under President Bush, only embryonic stem cell
lines in existence before August 9, 2001 were allowed for federally
funded research (which was significant considering most university
biotech researchers involves some degree of federal funding).
Newer lines were expressly
forbidden from federal funding.
Now, President Barack
Obama's administration has thrown
that policy away according to the New York Times, allowing
the first of many new embryonic stem cell lines to be approved.
The National Institutes of Health announced Wednesday that federal
researchers now have legal access to 13 new embryonic stem cell
lines. Over 96 more lines are under review and may soon be
approved.
Embryonic stem cells are typically derived from
embryos left over at in vitro fertility clinics. Opening more
lines is significant for many reasons. First, it is notoriously
hard to keep stem cells growing and dividing in their original state
for almost 10 years. Genetic changes may skew test results and
lead to misleading conclusions.
Secondly, it's important to
have multiple lines accessible to verify that phenomena observed are
applicable to all stem cells or just certain lines. This
information is essential if doctors are to ever hope to seriously
treat diseases on a widespread basis with stem cells.
During
the ban, researchers were able to finance some work on new lines via
independent financing, but found themselves buried under mounds of
government red tape, namely the necessity to keep the independently
financed lines in separate areas. Describes Ali H. Brivanlou, a
researcher at Rockefeller University, "You can imagine what it
meant not to be able to carry a pipette from one room to another.
They even had to repaint the walls to ensure no contamination by
federal funds."
Two of the new lines were derived via
private funding and through the work of Dr. Brivanlou's group.
Dr. George Daley of Children’s Hospital, Boston prepared the
remaining 11 lines. Dr. Francis S. Collins, director of the
health agency, says that despite the fact that researchers can't
derive their own lines, most understand that the decision to open up
more lines is a major step forward. He describes, "I’m
not sure everyone is interested in deriving their own cell lines as
long as they can get lines from others."
In recent years
the controversy over the ban on new stem-cell lines has eased
slightly with the discovery of induced
pluripotent stem cells (iPSCs). As time has passed, though,
iPSCs now appear a less viable option than previously thought.
Like embryonic stem cells, they require complex chemical and physical
stimuli to differentiate into the proper cell type. However,
unlike embryonic stem cells, they carry an additional tumorigenic
(cancer) risk due to the mutagenic agents used to force the cells
into pluripotency. New methods of induction are being devised,
but the risks largely remain to date.
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