Couple of years ago the whole of India witnessed what was called as the
‘Siachen Miracle'. Lance Naik Hanumanthappa Koppad, aged 32, an Indian
brave heart Soldier,(one of those 9 Indian soldiers on duty in the
treacherous Siachen Glaciers who were struck by a sudden snow avalanche)
had defied certain death and survived for all of six days, buried under
snow, until succumbing later to multi organ failure, pneumonia and
blood clotting at the Army Hospital in Delhi, where he was airlifted
from Siachen. It is generally believed by experts that nearly 90% of
completely buried avalanche victims can be revived if and only if they
are recovered within 15 minutes. The chances of survival beyond a day
are almost non existent. But then was it a miracle that Hanumanthappa
could survive for six days under the wall of snow? Perhaps not. The
science underpinning the so called miracle of Hanumanthappa’s survival,
can now be explained in the works of this year’s Noble laureates in
Physiology or Medicine, who have been awarded this year’s Nobel prize
for their work on 'how cells adapt to oxygen availability’. The
significance of their work can best be seen in the statement of Venki
Ramakrishnan, President of Britain’s Royal Society, who said ‘Oxygen is
the vital ingredient for the survival of every cell in our bodies. Too
little – or too much – can spell disaster. Understanding how evolution
has equipped cells to detect and respond to fluctuating oxygen levels
helps answer fundamental questions,”. He added, “This work.. also gives
insights into the way these processes continue to shape our health and
wellbeing.”
The three physician researchers; William G Kaelin,
Sir Peter Ratcliffe and Gregg L Semenza have been jointly awarded this
year’s Noble prize in Physiology or Medicine for their research on
Hypoxia. The three of them - physicians as well as scientists - share an
astounding prize money of 9 Million Swedish Krone (7.41 Crore ₹). One
third of the prize money goes to William Kaelin, a Howard Hughes
investigator at the Dana-Farber Cancer Institute at Harvard. One third
to Gregg Semenza, who is at the Johns Hopkins University. And the third
part of the prize money goes to Sir Peter Ratcliffe, who is with the
Oxford University. Their combined research work has established the
basis for understanding of how oxygen levels are sensed by cells, a
discovery that is being explored by medical researchers seeking to
develop treatments for various diseases that work by either activating
or blocking the body's oxygen-sensing machinery. Their work centres on
the hypoxic response - the way the body reacts to oxygen flux - and
reveals the elegant mechanisms by which our cells sense oxygen levels
and respond. The statement of the Nobel prize announcing committee says
“The seminal discoveries by this year’s Nobel Laureates revealed the
mechanism for one of life’s most essential adaptive processes. They
established the basis for our understanding of how oxygen levels affect
cellular metabolism and physiological function. Their discoveries have
also paved the way for promising new strategies to fight anaemia, cancer
and many other diseases.”
Oxygen is inextricably linked to life
on planet Earth and it is used by the mitochondria, present virtually in
all animal cells, to convert food into useful energy. The Oxygen we
inhale, through our lungs, crosses over into tiny blood vessels, where
it piggybacks on the hemoglobin protein - that are present in red blood
cells- to serve as the life delivering services in human system. The Red
blood cells (RBC) transport oxygen to each tissue where the cells let
in just enough oxygen to carry out a precise amount of work. However the
body has to adjust its requirements of oxygen to different atmospheric
conditions of the planet and in different situations. How and what cell
mechanism is used to sense the precise requirements of oxygen in
different conditions had remained a mystery until the works of this
year’s Nobel laureates made head way in unravelling it. Moreover there
aren’t consistent levels of oxygen available everywhere on this planet.
For example the higher the altitude we travel (Siachen or the
Himalayas), the thinner the air, and less the presence of oxygen and
this condition is called hypoxia. Our cells need to make more or less
energy depending on the place where we are or whether we are active or
sedentary and accordingly we need more or less oxygen. This year’s Nobel
laureates have conducted years of research that helps explain how cells
sense oxygen levels, and how they adapt to higher or lower amounts of
the molecules in the atmosphere. When the body detects that less oxygen
is present, the kidneys release a hormone called erythropoietin, or EPO,
which tells the body to make more red blood cells to carry more oxygen
around (erythropoiesis).The importance of hormonal control of
erythropoiesis was already known at the beginning of the 20th century,
but how this process was itself controlled by Oxygen had remained a
elusive.
Decades of work from Semenza and Ratcliffe identified
how this system works in more detail. They found that a protein called
hypoxia-inducible factor, or HIF, rises when there is less oxygen
around. HIF then bonds to sections of DNA near the gene that produces
EPO. Extra HIF protein around the EPO gene acts like a turbo charge for
the hormone’s production, which is how the body knows to make more RBC.
When there’s sufficient oxygen available, HIF levels drop, as do RBC
counts. These were important findings that showed the mechanism was
general and functional in many different cell types.
It was
around this time that William Kaelin, Jr. a cancer physician was
researching on an inherited syndrome, von Hippel-Lindau's disease (VHL
disease). This genetic disease leads to dramatically increased risk of
certain cancers in families with inherited VHL mutations. Kaelin showed
that the VHL gene encodes a protein that prevents the onset of cancer.
Kaelin also showed that cancer cells lacking a functional VHL gene
express abnormally high levels of hypoxia-regulated genes; but that when
the VHL gene was reintroduced into cancer cells, normal levels were
restored. This was an important clue showing that VHL was somehow
involved in controlling responses to hypoxia. Additional clues came from
several research groups showing that VHL is part of a complex that
labels proteins with ubiquitin, marking them for degradation in the
proteasome. Ratcliffe and his research group then made a key discovery:
demonstrating that VHL can physically interact with HIF-1alpha and is
required for its degradation at normal oxygen levels. This conclusively
linked VHL to HIF-1alpha.
The discovery of a molecular switch
that regulates how cells adapt to fluctuating oxygen levels have opened
up new approaches to treating heart failure, anaemia and cancer. Now
that the scientists know and have understood how the body regulates
oxygen uptake, they can now develop new therapies for individuals for
whom that process has gone wrong and help in saving millions of lives.
Long live oxygen the life sustainer on Earth.
1 comment:
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Oxygen
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