Haim Y. Cohen1,2,3,4, Christine Miller1,2,3,4, Kevin J. Bitterman1,2,3,4, Nathan R. Wall1,2,3,4, Brian Hekking1,2,3,4, Benedikt M. Kessler1,2,3,4, Konrad T. Howitz1,2,3,4, Myriam Gorospe1,3,4, Rafael de Cabo1,3,4, David Sinclair1,2,3,4
1BIOMOL Research Laboratories, 5120 Butler Pike, Plymouth Meeting, PA 19462, USA.
2Department of Pathology, Harvard Medical School, 77 Avenue Louis Pasteur, Boston, MA 02115, USA
3Laboratory of Cellular and Molecular Biology, Post Office Box 12, Gerontology Research Center, National Institute on Aging, National Institutes of Health, 5600 Nathan Shock Drive, Baltimore, MD 21224, USA.
4Laboratory of Experimental Gerontology, Post Office Box 12, Gerontology Research Center, National Institute on Aging, National Institutes of Health, 5600 Nathan Shock Drive, Baltimore, MD 21224, USA.
Tóm tắt
A major cause of aging is thought to result from the cumulative effects of cell loss over time. In yeast, caloric restriction (CR) delays aging by activating the Sir2 deacetylase. Here we show that expression of mammalian Sir2 (SIRT1) is induced in CR rats as well as in human cells that are treated with serum from these animals. Insulin and insulin-like growth factor 1 (IGF-1) attenuated this response. SIRT1 deacetylates the DNA repair factor Ku70, causing it to sequester the proapoptotic factor Bax away from mitochondria, thereby inhibiting stress-induced apoptotic cell death. Thus, CR could extend life-span by inducing SIRT1 expression and promoting the long-term survival of irreplaceable cells.
