TY - JOUR
T1 - The life span-prolonging effect of sirtuin-1 is mediated by autophagy
AU - Morselli, Eugenia
AU - Maiuri, Maria Chiara
AU - Markaki, Maria
AU - Megalou, Evgenia
AU - Pasparaki, Angela
AU - Palikaras, Konstantinos
AU - Criollo, Alfredo
AU - Galluzzi, Lorenzo
AU - Malik, Shoaib Ahmad
AU - Vitale, Ilio
AU - Michaud, Mickael
AU - Madeo, Frank
AU - Tavernarakis, Nektarios
AU - Kroemer, Guido
N1 - Funding Information:
N.T. is supported by grants from EMBO, the European Research Council (ERC) and the European Commission Coordination Action ENINET (con tract number LSHM-CT-2005-19063). G.K. is supported by the Ligue Nationale contre le Cancer (Equipes labellisée), Agence Nationale pour la Recherche (ANR), European Commission (Apo-Sys, ChemoRes, ApopTrain, Active p53), Fondation pour la Recherche Médicale (FRM), Institut National du Cancer (INCa) and Cancéropôle Ile-de-France. E.M. was founded by a PhD student grant from ApopTrain.
PY - 2010/1/1
Y1 - 2010/1/1
N2 - The life span of various model organisms can be extended by caloric restriction as well as by autophagyinducing pharmacological agents. Life span-prolonging effects have also been observed in yeast cells, nematodes and flies upon the overexpression of the deacetylase Sirtuin-1. Intrigued by these observations and by the established link between caloric restriction and Sirtuin-1 activation, we decided to investigate the putative implication of Sirtuin-1 in the response of human cancer cells and Caenorhabditis elegans to multiple triggers of autophagy. Our data indicate that the activation of Sirtuin-1 (by the pharmacological agent resveratrol and/or genetic means) per se ignites autophagy, and that Sirtuin-1 is required for the autophagic response to nutrient deprivation, in both human and nematode cells, but not for autophagy triggered by downstream signals such as the inhibition of mTOR or p53. Since the life spanextending effects of Sirtuin-1 activators are lost in autophagy-deficient C. elegans, our results suggest that caloric restriction and resveratrol extend longevity, at least in experimental settings, by activating autophagy.
AB - The life span of various model organisms can be extended by caloric restriction as well as by autophagyinducing pharmacological agents. Life span-prolonging effects have also been observed in yeast cells, nematodes and flies upon the overexpression of the deacetylase Sirtuin-1. Intrigued by these observations and by the established link between caloric restriction and Sirtuin-1 activation, we decided to investigate the putative implication of Sirtuin-1 in the response of human cancer cells and Caenorhabditis elegans to multiple triggers of autophagy. Our data indicate that the activation of Sirtuin-1 (by the pharmacological agent resveratrol and/or genetic means) per se ignites autophagy, and that Sirtuin-1 is required for the autophagic response to nutrient deprivation, in both human and nematode cells, but not for autophagy triggered by downstream signals such as the inhibition of mTOR or p53. Since the life spanextending effects of Sirtuin-1 activators are lost in autophagy-deficient C. elegans, our results suggest that caloric restriction and resveratrol extend longevity, at least in experimental settings, by activating autophagy.
KW - Aging
KW - Beclin 1
KW - Rapamycin
KW - Senescence
KW - Spermidine
KW - Starvation
UR - http://www.scopus.com/inward/record.url?scp=75149128169&partnerID=8YFLogxK
U2 - 10.4161/auto.6.1.10817
DO - 10.4161/auto.6.1.10817
M3 - Article
AN - SCOPUS:75149128169
SN - 1554-8627
VL - 6
SP - 186
EP - 188
JO - Autophagy
JF - Autophagy
IS - 1
ER -