If you had the choice, would you like to live until you’re 130
years old? New research in fruit flies shows that manipulating a single gene can
extend their lifespan up to 60%, suggesting that living well into your hundreds
might become a reality in the foreseeable future.
Dying of old age is a strange thing. Why does our
health decline just because we’re old? Although the answer might at first seem
obvious or simple, it really isn’t. There are countless theories of ageing, a
few popular even outside the scientific community. Take ‘superfoods’, for
example. The miracle properties credited to these antioxidant-rich foods stem
from the free radical theory of ageing—older
cells produce more of a toxic form of oxygen that gradually poisons them. Antioxidants
like vitamin C or D counteract this deleterious effect and prevent ageing (and
the appearance of wrinkles), superfood advocates claim.
A common denominator in these theories is that we age—and
ultimately die—because our cells deteriorate with time (for whatever reason). As
tissues and organs mount up more and more of these damaged cells, they begin to
malfunction and eventually stop working. This raises an interesting assumption.
What if we could get rid of these unfit cells and keep only the healthy ones?
Would we live longer?
It’s well known that sick cells such as cancerous cells, are eliminated by our bodies, either by immune cells or by committing suicide. However,
our ‘old’ unfit cells are still healthy enough to bypass this quality-control checkpoint.
Or so it was thought. A few years ago, Eduardo Moreno and colleagues at the
University of Bern, Switzerland, showed that healthy but less fit cells are also culled from tissues, by a mechanism they called “fitness fingerprints”. Each
cell has a molecular fingerprint on its surface that tells its neighbours how
healthy it is. When a given cell has a fingerprint that is worse than its
neighbours', it kills itself. But the researchers didn’t know the importance of this cell elimination process for the organism. For example, would
we age faster if those cells could not kill themselves?
To answer these questions, Moreno’s team genetically
engineered fruit flies to control a newly found gene essential for marking
unfit cells for culling. “If you put an extra copy of this gene you have better
selection of the [unfit] cells, they are eliminated faster and therefore the
animals can live longer”, says Moreno.
When the gene, which Moreno named azot, was removed from flies, they became sick and died prematurely.
On the other hand, flies with an extra copy of the azot gene lived up to 60% longer.
Previously, only caloric restriction had been shown to
prolong lifespan to such an extent in flies. In fact, reducing the amount of
daily calorie input increases longevity in flies, nematodes, fish, mice and
rats (data from studies with primates remain controversial). Could it be then,
that starved flies with an extra copy of the azot gene live even longer? Indeed, these flies lived about
80% longer, Moreno’s team showed. In human time this would be equivalent to
living up to 150 years!
The question remains whether these findings could be
relevant for our species. Humans have the azot
gene, in fact most organisms do, so potentially it should be possible to
increase life expectancy in people by altering azot protein levels.
“You could start thinking of how to manipulate these
mechanisms with drugs, for example, to treat ageing or diseases like neurodegeneration
or myocardial infarction,” says Moreno, “I’m totally convinced it
will be possible to delay aging and prolong lifespan in humans.”
Would we want to live longer though, if we spend most
of our life old and sick? “Our long-term challenge will be to understand the
biology of aging to address problems associated with steadily increasing life
expectancy, such as metabolic disease and neurodegeneration”, says Martin
Denzel, a researcher at the Max Planck Institute for Biology of Ageing in
Cologne, Germany. With this in mind, Moreno’s team tested whether the long-living
azot flies remained healthy as they aged. When the researchers looked in these
flies’ brains, they found that their neurons accumulated fewer ageing cellular
markers. Azot not only prolongs lifespan, but it also delays ageing.
In the future the team wants to understand what azot is actually doing. This gene
encodes for a protein of unknown function, but the researchers know that when “the
azot gene is activated, it triggers
the normal cell death apoptosis pathway”, Moreno concludes. The team will also investigate
the function of azot in mice, and
collaborate with medical doctors to see if the azot-dependent cell elimination pathways are present in
ageing-related diseases like Alzheimers.
“I have high hopes that eventually basic research into
the aging process will yield treatments that extend the span of healthy living
and that improve the quality of life in advanced age”, Denzel explains. “However,
it will take a lot of additional work to investigate if this mechanism might be
beneficial in mammals.”
Reference:
Reference:
Merino M., Jesus M. Lopez-Gay, David Buechel, Barbara Hauert & Eduardo Moreno (2015). Elimination of Unfit Cells Maintains Tissue Health and Prolongs Lifespan, Cell, DOI: http://dx.doi.org/10.1016/j.cell.2014.12.017
This article was published in Lab Times on the 23-01-2015. You can read it here.