Aging research indicates that better healthspan--the quality of life as we age--may be more important than lifespan.
In a report published in Nature Communications, a surprising new genetic discovery by researchers suggests that there may be molecular switches that control lifespan and healthspan separately.
Healthspan is represented by a set of parameters like mobility and immune resistance that are distinct from lifespan, which can be easily measured. Though it is harder to study, in the long run, it may be more relevant to modify healthspan, notes the senior author. "The goddess Eos fell in love with a mortal man, Tithonus, and asked that he be granted eternal life, but forgot to ask for eternal youth. Tithonus lived forever but as a frail and immobile old man."
In the current study, the team focused on a protein called TCER-1 in the worm Caenorhabditis elegans. Earlier work from their lab showed that TCER-1 promotes longevity in worms and also is critical to its fertility.
Longevity genes in many animals increase resistance to stressors, such as infection, so the researchers expected that removing TCER-1 would make the worms less resilient.
Much to their surprise, they saw the exact opposite. When infected with bacteria, subjected to DNA-damaging radiation or high temperatures, worms without TCER-1 survived much longer than normal worms. They also had improved mobility with age and were less prone to protein clumping that causes human neurodegenerative diseases. Conversely, increasing TCER-1 levels beyond normal suppressed the animal's immune defenses.
"I was sure I'd made a mistake somewhere," says the study's lead author. "But I repeated the experiments and realized that TCER-1 was unlike any other longevity gene we'd seen before--it was actually suppressing immune resistance."
Interestingly, TCER-1 seemed to be able to wield its influence only as long as the animals were young and capable of laying eggs. The authors show that the TCER-1 acts through repression of PMK-1 as well as PMK-1-independent factors critical for innate immunity.
"I liken TCER-1 in C. elegans to a DJ who controls the base, treble and other tones to get the music to sound just right," says the lead. "During its reproductive age, TCER-1 tunes all the molecular dials to ensure that the animal reproduces efficiently to propagate the species, partly by diverting resources meant for stress management."
The senior author cautions that it is too soon to make any conclusions about human healthspan, but notes that the finding should change how we understand the molecular basis of aging.
"It will be interesting to understand how the body allocates resources," the senior author speculates. "For example, could women one day take a pill once they decide to stop having children that would improve their healthspan by diverting resources used for reproduction toward improved stress resilience?"
Longevity and healthier living controlled by separate factors?
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