UCLA Biologists Slow Aging, Extend Lifespan of Fruit Flies

著者：   アップロード：2017-09-07  閲読回数：

    UCLA scientists working with middle-aged fruit flies say they were able to improve the insects' health while significantly slowing down their aging process. The team thinks its technique could eventually lead a way to delay the onset of Parkinson's disease, Alzheimer's disease, cancer, stroke, cardiovascular disease, and other age-related diseases in humans.

    The researchers zeroed in on mitochondria, which often become damaged with age. When cells can't eliminate the damaged mitochondria, they can become toxic and contribute to a wide range of age-related diseases, said David Walker, Ph.D., a UCLA professor of integrative biology and physiology, and the study's senior author.

    Dr. Walker and his colleagues found that as fruit flies reach middle age—about one month into their two-month lifespan—their mitochondria change from their original small, round shape.

    "We think the fact that the mitochondria become larger and elongated impairs the cell's ability to clear the damaged mitochondria," he said. "And our research suggests dysfunctional mitochondria accumulate with age, rather than being discarded."

    The study ("Promoting Drp1-Mediated Mitochondrial Fission in Midlife Prolongs Healthy Lifespan of Drosophila melanogaster"), published in Nature Communications, reports that the UCLA scientists removed the damaged mitochondria by breaking up enlarged mitochondria into smaller pieces and that when they did, the flies became more active and more energetic and had more endurance. Following the treatment, female flies lived 20% longer than their typical lifespan, while males lived 12% longer, on average. The research highlights the importance of the protein Drp1 in aging, at least in flies and mice, where levels of Drp1 drop with age.

    "We find that short-term induction of Drp1, in midlife, is sufficient to improve organismal health and prolong lifespan, and observe a midlife shift toward a more elongated mitochondrial morphology, which is linked to the accumulation of dysfunctional mitochondria in aged flight muscle. Promoting Drp1-mediated mitochondrial fission, in midlife, facilitates mitophagy and improves both mitochondrial respiratory function and proteostasis in aged flies," write the investigators.

    "Finally, we show that autophagy is required for the anti-aging effects of midlife Drp1-mediated mitochondrial fission. Our findings indicate that interventions that promote mitochondrial fission could delay the onset of pathology and mortality in mammals when applied in midlife."

    To break apart the flies' mitochondria, Anil Rana, Ph.D., a UCLA project scientist and the study's lead author, increased their levels of Drp1. This enabled the flies to discard the smaller, damaged mitochondria, leaving only healthy mitochondria. Drp1 levels were increased for one week starting when the flies were 30 days old.

    At essentially the same time, Dr. Rana demonstrated that the flies' Atg1 gene also plays an essential role in turning back the clock on cellular aging. He did this by "turning off" the gene, rendering the flies' cells unable to eliminate the damaged mitochondria. This proved that Atg1 is required to reap the procedure's antiaging effects: While Drp1 breaks up enlarged mitochondria, the Atg1 gene is needed to dispose of the damaged ones.

    "It's like we took middle-aged muscle tissue and rejuvenated it to youthful muscle," said Dr. Walker, a member of UCLA's Molecular Biology Institute. "We actually delayed age-related health decline. And seven days of intervention was sufficient to prolong their lives and enhance their health."

    One specific health problem the treatment addressed was the onset of leaky intestines, which previous research by Walker's team found commonly occurs about a week before fruit flies die. Subsequent research in other laboratories has determined that an increase in intestines' permeability is a hallmark of aging in worms, mice, and monkeys. In the UCLA study, the condition was delayed after flies were given more Drp1.

    Dr. Walker hopes that a technique similar to the one his team developed for fruit files could eventually help humans by slowing aging and delaying aging-related diseases. He said the fact that the new approach was effective, even after a short time, is especially significant because long-term use of nearly any drug can have harmful side effects in humans.

    One of the long-term goals of his research is to develop pharmaceuticals that would mimic the effects of Drp1, in order to extend people's lives and lengthen what he calls people's "healthspans," meaning the number of healthy years in their lives.

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