A shot of young stem cells made rapidly
aging mice live longer and healthier
January 5, 2012– Mice bred to age too
quickly seemed to have sipped from the
fountain of youth after scientists at the
University of Pittsburgh School of Medicine
injected them with stem cell-like progenitor
cells derived from the muscle of young,
healthy animals.
Instead of becoming infirm and dying early
as untreated mice did, animals that got the
stem/progenitor cells improved their health
and lived two to three times longer than
expected, according to findings published in
the Jan. 3 edition ofNature
Communications.
Previous research has revealed stem cell
dysfunction, such as poor replication and
differentiation, in a variety of tissues in
old age, but it's not been clear whether
that loss of function contributed to the
aging process or was a result of it,
explained senior investigators Johnny Huard,
Ph.D., and Laura Niedernhofer, M.D., Ph.D.
Dr. Huard is professor in the Departments of
Orthopaedic Surgery and of Microbiology and
Molecular Genetics, Pitt School of Medicine,
and director of the Stem Cell Research
Center at Pitt and Children's Hospital of
PIttsburgh of UPMC. Dr. Niedernhofer is
associate professor in Pitt's Department of
Microbiology and Molecular Genetics and the
University of Pittsburgh Cancer Institute
(UPCI).
"Our experiments showed that mice that have
progeria, a disorder of premature aging,
were healthier and lived longer after an
injection of stem cells from young, healthy
animals," Dr. Niedernhofer said. "That tells
us that stem cell dysfunction is a cause of
the changes we see with aging."
Their team examined a stem/progenitor cell
population derived from the muscle of
progeria mice and found that compared to
those from normal rodents, the cells were
fewer in number, did not replicate as often,
didn't differentiate as readily into
specialized cells and were impaired in their
ability to regenerate damaged muscle. The
same defects were discovered in the
stem/progenitor cells isolated from very old
mice.
"We wanted to see if we could rescue these
rapidly aging animals, so we injected
stem/progenitor cells from young, healthy
mice into the abdomens of 17-day-old
progeria mice," Dr. Huard said. "Typically
the progeria mice die at around 21 to 28
days of age, but the treated animals lived
far longer – some even lived beyond 66 days.
They also were in better general health."
As the progeria mice age, they lose muscle
mass in their hind limbs, hunch over,
tremble, and move slowly and awkwardly.
Affected mice that got a shot of stem cells
just before showing the first signs of aging
were more like normal mice, and they grew
almost as large. Closer examination showed
new blood vessel growth in the brain and
muscle, even though the stem/progenitor
cells weren't detected in those tissues.
In fact, the cells didn't migrate to any
particular tissue after injection into the
abdomen.
"This leads us to think that healthy cells
secrete factors to create an environment
that help correct the dysfunction present in
the native stem cell population and aged
tissue," Dr. Niedernhofer said. "In a
culture dish experiment, we put young stem
cells close to, but not touching, progeria
stem cells, and the unhealthy cells
functionally improved."
Animals that age normally were not treated
with stem/progenitor cells, but the
provocative findings urge further research,
she added. They hint that it might be
possible one day to forestall the biological
declines associated with aging by delivering
a shot of youthful vigor, particularly if
specific rejuvenating proteins or molecules
produced by the stem cells could be
identified and isolated.