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Turning Back the Reproductive Clock
Reported August 31, 2009
(Ivanhoe Newswire) – Scientific dogma has long asserted that females
are born with their entire lifetime supply of eggs, and once they're gone,
they're gone. New findings suggest that in nematode worms, at least, this is
not necessarily so.
Molecular physiologist Marc Van Gilst, Ph.D., and colleagues at Fred
Hutchinson Cancer Research Center in Seattle report that during starvation,
sexually mature adult worms stop ovulating and the germline component of
their reproductive system – the sex cells, including mature and maturing
eggs – dies off and leaves behind nothing but a few stem cells. However,
once normal food conditions resume, the conserved stem cells can produce a
brand new crop of sex cells, complete with youthful fertile eggs. This
turning back of the reproductive clock took place in tiny C. elegans soil
worms that were up to15 times older than worms in their reproductive prime
that were fed normally.
"For many, it has been assumed that cells and organs remain relatively
stable during periods of starvation or caloric restriction," Van Gilst, an
assistant member of the Hutchinson Center's Basic Sciences Division, who
authored the study with postdoctoral research fellow Giana Angelo, Ph.D is
quoted as saying. "The idea that an entire system would kill itself off
during starvation and then regenerate upon food restoration was very
surprising. The fact that extremely old worms could generate new eggs and
produce healthy offspring long after their normally fed counterparts had
reproduced and died was also unexpected."
The mechanism behind the preservation and extension of fertility long past
the worms' normal reproductive prime, Van Gilst suspects, is a signaling
receptor protein in the cell nucleus called NHR-49, which promotes a major
metabolic response to dietary restriction and fasting. While it has been
hypothesized that this protein may interface with calorie restriction to
extend life span, until now its role in protecting and extending
reproductive longevity in the face of starvation had not been known. "In
worms that contained an inactive NHR-49 gene, reproductive recovery and
fertility after starvation were severely impaired," he said. "We found that
reproductive arrest and recovery are highly dependent on a functioning
NHR-49 gene."
NHR-49 in worms is analogous to various proteins in humans called nuclear
receptors. Nuclear receptors, such as estrogen receptors and androgen
receptors, are particularly good targets for pharmaceutical intervention.
"The identification of a nuclear receptor that turns on and off the
beneficial response to nutrient deprivation would be of great interest
because it would be a candidate for drugs aimed at tricking the body, or
specifically the reproductive system, into thinking they are calorically
restricted or starved, even when food intake is normal," Van Gilst said.
The biomedical implications of model organisms such as flies and worms
cannot be overlooked, he said. "Many paradigm-shifting discoveries in C.
elegans have since been replicated in humans.” he said. “Therefore, the idea
that our findings will be relevant to human reproduction is a possibility
that certainly needs exploration."
Van Gilst was quick to point out, however, that even if this mechanism is
conserved in humans, researchers still do not know the degree of caloric
restriction that would be required to impact egg production in humans. "If
such a process exists in humans, it likely evolved to help our ancestors
preserve fertility during periods of famine or food shortage,” he said. “We
certainly don't have a prescription for famine. Consequently, our study
should not be used to promote potentially dangerous interventions such as
severe caloric restriction and starvation as a means to restore a woman's
fertility."
In the meantime, Van Gilst and colleagues will continue to study the tiny
worm to better understand the mechanisms that control fertility. One
question their research may address is how women recovering from radiation
and bone marrow transplant – which damages or destroys much of the germline,
including mature and immature eggs – can regain their fertility.
"There is controversy over how this occurs," Van Gilst said. "On the one
hand, it has been argued that new eggs are generated from the woman's
germline stem cells through a process that may mirror the germline
regeneration we observed in C. elegans. In fact, there is controversy over
whether or not germline stem cells exist in adult women. We believe that our
work in C. elegans throws another hat in the ring, raising the possibility
that germline stem cells may indeed be present in women and that their
activity may surface under conditions of nutrient deprivation or stress," he
said.
This work may also shed new light on cancer. "Cancer cells, when starved,
are very susceptible to cell death. However, cancer stem cells, or
progenitor cells, often thrive and flourish during starvation in
cell-culture experiments. When nutrition is restored, these cells can
trigger rapid regrowth,” he said. “Consequently, understanding how germline
stem cells in C. elegans survive starvation may help appreciate how cancers
survive treatments aimed at starving tumors."
SOURCE: Science, August 27, 2009 |
