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With the threat of an obesity crisis looming,
a study led by UCL researchers reveals today that fat tissue isn't
always the enemy. Reporting in the journal Science they show that
a molecular signalling pathway in fat tissue is an important mediator
in extending lifespan.
The study, conducted on one of scientists' favourite model organisms
- the fruit fly - found that reducing activity of the insulin/insulin-like
growth factor (IIS) signalling pathway in fat tissue of adults
extended life by up to 50 per cent.
Previously it has been shown that reducing the activity of the
IIS pathway extends lifespan in fruit flies, mice and the worm
C. elegans. But the cellular processes that determine longevity
were not understood.
Results suggest the system that governs longevity evolved in
a precursor of all three species and is likely to be conserved
in humans.
Professor Linda Partridge of UCL's Department of Biology, and
senior author of the study, says:
"Basically, we are learning that nearly everything in biology
is highly conserved. For years biologists studying ageing were
convinced that it just happened and there wouldn't be genes that
controlled it - you just wore out. But it became apparent independent
of weight or size, some animals live much longer than others.
"Researchers became intrigued that on average a mouse lives
for two years, a canary for 13 and a bat for 50 yet these species
are all around the same size and warm blooded. A tortoise lives
for up to one hundred years, but humans live for only 75. This
suggests there must be a genetic determinant of the rate of ageing
and these regulatory mechanisms can be set differently in different
species. All we have to do is crack the code to reset the clock
and our research takes this a step closer."
The possibility of extending life span has preoccupied scientists
for many years. Leading theories include the idea that eating
less slows down the progressive damage caused by free radicals
that are released when oxygen is used to breakdown fats and carbohydrates.
But another theory is that calorie restriction does something
critical to the insulin-signalling pathway that helps regulate
how glucose is used by the body.
Dr Maria Giannakou of UCL's Department of Biology, who led the
study, explains:
"Studies in rats have shown restricting diet doubles lifespan
but the pay off is reduced fertility. Elsewhere, groups have looked
at mutations such as the DAF-2 gene in C. elegans, which can also
double life span or reduce fertility depending on what stage in
life the gene is interfered with.
"DAF-2 encodes the worms' equivalent of the human insulin
receptor and as such form part of the IIS pathway. As animals
on restricted diets are far less likely to get diabetes and related
disorders, this suggests that genes involved in glucose metabolism
might be linked to the genes involved in ageing."
Previous studies have shown reducing DAF-2 function during development
affects only fertility, but in adulthood reducing function affects
only lifespan. The researchers concluded that the two effects
influenced different parts of the IIS pathway and their affects
could be isolated.
Efforts focussed on a key target in the IIS pathway in the fruit
fly, dFOXO. Known as a transcription factor, it helps activate
and regulate genes.
They found that increasing levels of the transcription factor
dFOXO in the fat cells of female fruit flies from the onset of
adulthood increased lifespan by between 20 and 50 per cent and
reduced fertility by 50 per cent. But no effect was observed in
male flies.
"The functions of fruit fly fat include many of the metabolic
activities of mammalian liver and fat storage. In mice deletion
of insulin receptors in white fat cells results in a lean long
living adult. Together this suggests that fat tissue is crucial
in extending lifespan by altering the IIS pathway," said
Dr Giannakou.
"Further work needs to be done to determine why there is
a different affect in both sexes," added Professor Partridge.
"It could be because females are more influenced by food
and its consequences. They make things - eggs, babies, and need
a lot of nutrients for this. Males tend to move around a lot -
to find females and persuade them to mate, and need less nutrients
to make things. But this is just speculation."
The study was funded by the Wellcome Trust and the Biotechnology
and Biological Science Research Council.
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