PITTSBURGH – June 23, 2005 – In a ground-breaking study, scientists at
Children’s Hospital of Pittsburgh have discovered that adult, or post-natal,
stem cells have the same ability as embryonic stem cells to multiply, a
previously unknown characteristic indicating that post-natal stem cells may
play an important therapeutic role.
Adult and post-natal stem cells are often overlooked in favor of
embryonic stem cells in the national debate over the therapeutic use of stem
cells. Until now, it has been generally believed that embryonic stem cells
had a greater capacity to multiply than post-natal stem cells, making them
more desirable to research as a potential treatment, according to Johnny
Huard, PhD, director of the Growth and Development Laboratory at Children’s
Hospital of Pittsburgh.
“Scientists have typically believed that adult or post-natal stem
cells grow old and die much sooner than embryonic stem cells, but this study
demonstrates that is not the case,” said Dr. Huard, senior author of the
study. “The entire world is closely following the advances in stem cell
research, and everyone is interested in the potential of stem cells to treat
everything from diabetes to Parkinson’s disease. But there are also many
ethical concerns surrounding the use of embryonic stem cells, concerns that
you don’t have with post-natal or adult stem cells. My belief is that this
study should erase doubts scientists may have had about the potential
effectiveness of post-natal stem cells.”
Researchers from Children’s and the University of Pittsburgh in Dr.
Huard’s laboratory were able to expand post-natal stem cells to a population
level comparable to that reached by researchers using embryonic stem cells.
Previous research has found that embryonic stem cells could undergo more
than 200 population doublings before the cells began to die. A population
doubling is a method of measuring the age of a population of cells.
Bridget Deasy, PhD, a scientist in Dr. Huard’s laboratory, was
first author of the study. Dr. Deasy, a research assistant professor in the
Department of Orthopaedic Surgery at the University of Pittsburgh School of
Medicine, discovered that a unique population of muscle-derived stem cells
was able to undergo more than 200 population doublings, as well. These
post-natal cells were able to undergo population doublings while maintaining
their ability to regenerate muscle in an animal model, a key finding
indicating that they could maintain their treatment potential.
This ability to self-replenish is significant because in order for
stem cells to be used for treatment, a large quantity of the cells would be
required.
The findings are published in the July 1, 2005, issue of Molecular
Biology of the Cell, published by the American Society for Cell Biology. The
paper is under consideration for Molecular Biology of Cell paper of the
year.
There also may be important advantages to post-natal stem cells
when it comes to autoimmunity, according to Dr. Huard, deputy director of
the McGowan Institute of Regenerative Medicine and associate professor of
Orthopaedic Surgery, Molecular Genetics and Biochemistry, and Bioengineering
at the University of Pittsburgh School of Medicine.
The use of embryonic stem cells could be complicated by issues of
rejection, with the recipient’s immune system rejecting the foreign
embryonic stem cells. With post-natal stem cells taken from the recipient
and then reintroduced in an autologous manner, rejection would not be an
issue.
Dr. Huard is one of the world’s top cell biologists researching
the potential therapeutic use of stem cells. He currently is working with
the stem cells he discovered while searching for a cure for Duchene muscular
dystrophy (DMD), a genetic disease that is estimated to affect one in every
3,500 boys. DMD is the most common form of muscular dystrophy affecting
children and patients often die in early adulthood because of heart damage.
In addition to searching for a cure for DMD, Dr. Huard’s
laboratory also is researching the use of stem cells to repair injured
muscle following sports-related injuries, as well as to treat cardiac, joint
and bone injuries. His work with these stem cells has potential implications
ranging from repairing heart muscle damaged by heart attack or disease to
the prevention of rejection during organ and tissue transplantation.
View the
study, "Long-Term Self-Renewal of Post-Natal Muscle-Derived Stem Cells."
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