Eliminating Germline Lengthens Fly Lifespan, Study Shows (4/26/2008)

Brown University biologists have found that eliminating germline stem cells, the cells that make eggs and sperm, lengthens the life of fruit flies and alters the insects' insulin production. These findings suggest a provocative general principle at work: Molecular signals from the reproductive system affect aging and metabolism in animals - and possibly in humans. The work also proposes a new mechanism of how this control may occur. Results are published in the Proceedings of the National Academy of Sciences.

New research by Brown University biologists shows that fruit flies live longer when they don't produce germline stem cells - the cells that create eggs and sperm.

The work suggests a provocative general principle at work: Signals from reproductive tissue directly control lifespan and metabolism in the whole organism. The work, which appears in the Proceedings of the National Academy of Sciences, also offers a first glimpse of how this control in the fly might occur at the molecular level.

"For more than 50 years, scientists have known that there is a link between reproduction and lifespan," said Thomas Flatt, a postdoctoral research associate in the Department of Ecology and Evolutionary Biology at Brown and the lead author of the research article. "When reproduction is delayed, animals live longer. Why? Our research suggests that signals from the reproductive system can regulate aging in animals - including, possibly, humans."

The Brown findings follow a seminal discovery made 10 years ago by acclaimed aging biologist Cynthia Kenyon at the University of California, San Francisco. Kenyon found that eliminating germline stem cells in roundworms extended their lifespan.

"We wanted to see if Kenyon's findings could be duplicated in the fly," said Marc Tatar, the senior scientist on the project and a professor in the Department of Ecology and Evolutionary Biology. "If so, we'd know that reproductive control of lifespan was a general principle in biology."

In their experiments, Flatt and Tatar over-activated a gene that controls germline stem cells in flies, a move that eliminated the cells' production. These sterile flies lived 20 to 50 percent longer than typical flies - results that matched Kenyon's finding in worms.

Flatt and Tatar speculated that these flies might live longer because they are insensitive to the effects of insulin. Past research at Brown and other universities shows that animals such as flies, worms and mice live longer when they produce or receive less insulin.

Yet, to their surprise, Flatt and Tatar found that when germline cells were eliminated, and flies lived longer, insulin-producing cells in the fly brain actually make more - not less - insulin. These results posed a paradox: How can flies be longer-lived when they're making more of a life-shortening hormone? When the researchers studied the flies' tissues, they discovered something intriguing: Even though the brains were making more insulin, the bodies were responding as if there was less insulin present.

Tatar said the team found a possible explanation for the paradox. In reaction to the flies' brains boosting insulin production, the insects' gonads - their ovaries or testes - produce a protein that acts like a sponge. This protein binds to the insulin and blocks its signals throughout the body. So the flies respond as if there is low, not high, insulin circulation inside their bodies.

"This suggests that the gonad and the brain are in a synchronized hormonal feedback loop," Tatar said. "It's not just the brain affecting the gonad, but also the other way around."

"We think that in mammals, a similar communication occurs between the brain and the gonad, communication which controls insulin signaling," Flatt said. "And when insulin signaling is reduced, the body goes into a state of high repair. The body becomes more stress resistant. Tissues protect themselves really well - and that increases longevity."

Eugenia Villa-Cuesta, a postdoctoral research associate in the Tatar lab, and John Cumbers, a graduate student in the Department of Molecular Biology, Cell Biology and Biochemistry, were part of the Brown research team, along with Kyung-Jin Min, a former postdoctoral research associate now at the University of Alaska, Anchorage. Ruth Lehmann of New York University School of Medicine and Cecilia D'Alterio and D. Leanne Jones of The Salk Institute for Biological Studies also contributed to the research.

The National Institute on Aging, The Howard Hughes Medical Institute, the Ellison Medical Foundation, the Roche Research Foundation, and the Swiss National Science Foundation funded the work.

Note: This story has been adapted from a news release issued by Brown University

Post Comments: