Spaceflight May Extend Lifespan of Microscopic Worm

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Caenorhabditis elegans (C. elegans)

The effect of spaceflight on a microscopic worm -- Caenorhabditis elegans (C. elegans) -- could help it to live longer. The discovery was made by an international group of scientists studying the loss of bone and muscle mass experienced by astronauts after extended flights in space.

The results of this research have been published today, July 5 2012, in the online journal Scientific Reports.

Dr Nathaniel Szewczyk, from The University of Nottingham, was part of the ICE-FIRST project which involved scientists from Japan, France, the US, and Canada. They discovered that spaceflight suppressed accumulation of toxic proteins that normally accumulate within aging muscle. They also discovered a group of genes that are expressed at lower levels during spaceflight. When the expression of these same genes were lowered in worms back on Earth the worms lived longer.

Dr Szewczyk, an expert in muscle metabolism, said: "We identified seven genes, which were down-regulated in space and whose inactivation extended lifespan under laboratory conditions." How do these genes play a role in longevity control?

"We are not entirely certain, but it would appear that these genes are involved in how the worm senses the environment and signals changes in metabolism in order to adapt to the environment. For example, one of the genes we have identified encodes insulin which, because of diabetes, is well known to be associated with metabolic control. In worms, flies, and mice insulin is also associated with modulation of lifespan."

What could this mean for space travellers?

"Well, most of us know that muscle tends to shrink in space. These latest results suggest that this is almost certainly an adaptive response rather than a pathological one. Counter-intuitively, muscle in space may age better than on Earth. It may also be that spaceflight slows the process of aging." Dr Szewczyk's role was to provide expertise in the culturing of worms in CeMM -- a special liquid food for worms. Dr Szewczyk transported the samples to and from the Russian launch site and ran a series of 'health' checks to ensure that the tiny astronauts were fit for flying. On their return he helped with the analysis of the data.

Nottingham's space biology lab

Dr Szewczyk studies the signals that control muscle protein degradation in the human body. C. elegans is the perfect substitute for studying long-term changes in human physiology because they suffer from muscle atrophy -- muscle loss -- under many of the same conditions that people do.

C. elegans was the first multi-cellular organism to have its genetic structure completely mapped and many of its 20,000 genes perform the same functions as those in humans. Two thousand of these genes have a role in promoting muscle function and 50 to 60 per cent of these have very obvious human counterparts. When the research began Dr Szewczyk was working at NASA. He is now based at The University of Nottingham's MRC and Arthritis Research UK Centre for Musculoskeletal Ageing Research. He is one of the leading scientists studying 'worms in space' and his lab is currently the most productive 'space biology' lab in the UK.

The experiment in 2004 involved a consignment of live worms being despatched to the International Space Station (ISS) onboard the Dutch DELTA mission. He uses worms which originate from a rubbish dump in Bristol. C. elegans often feed on decaying fruit and vegetable matter.

They have since taken part in five spaceflights to the ISS with the aim of learning more about the effect of microgravity on the physiology of the human body.

Notably, in 2003 Dr Szewczyk's C. elegans made the news when they survived the Space Shuttle Columbia disaster. Living in petri dishes and enclosed in aluminium canisters the worms survived re-entry and impact on the ground and were recovered weeks after the disaster.

This spaceflight work teaches us things about the body that we couldn't learn on Earth. They have led to the publication of research into how to block muscle degradation using a form of gene therapy in PLoS ONE and publication of a muscle repair mechanism in PLoS Genetics. The work on C. elegans has also established that worms can live and reproduce for at least six months in space. This makes it an ideal and cost-effective experimental system to investigate the effects of long duration and distance space exploration as recently reported in Interface, a journal of The Royal Society. Together these missions have established that the team is not only better able to understand how muscle works on Earth but they are also in a position to send worms to other planets and experiment on them along the way.

Astronaut now being studied

Another member of the Centre's team is currently examining the effects of spaceflight upon the muscles of the current European record holder for time spent in space.

Andre Kuipers, the Dutch astronaut who flew the mission in 2004, has just returned from ISS with yet another worm experiment from space for the team at Nottingham and is also, himself, being studied. That experiment, led by Professor Marco Narici, is to study the effects of long-duration spaceflight on human muscle.

Story credits

More information is available from Dr Nathaniel Szewczyk, at The University of Nottingham, on +44 (0)1332 724 615, nathaniel.szewczyk@nottingham.ac.uk

Genes down-regulated in spaceflight are involved in the control of longevity in Caenorhabditis elegans, Nature

Scientific Reports 2, Article number: 487 doi:10.1038/srep00487 Received 15 February 2012 Accepted 26 April 2012 Published 05 July 2012

"How microgravitational space environments affect aging is not well understood. We observed that, in Caenorhabditis elegans, spaceflight suppressed the formation of transgenically expressed polyglutamine aggregates, which normally accumulate with increasing age. Moreover, the inactivation of each of seven genes that were down-regulated in space extended lifespan on the ground. These genes encode proteins that are likely related to neuronal or endocrine signaling: acetylcholine receptor, acetylcholine transporter, choline acetyltransferase, rhodopsin-like receptor, glutamate-gated chloride channel, shaker family of potassium channel, and insulin-like peptide. Most of them mediated lifespan control through the key longevity-regulating transcription factors DAF-16 or SKN-1 or through dietary-restriction signaling, singly or in combination. These results suggest that aging in C. elegans is slowed through neuronal and endocrine response to space environmental cues."

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