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Suppression of Aging in Mice by the Hormone Klotho
Hiroshi Kurosu,1Masaya Yamamoto,1Jeremy D. Clark,1Johanne V. Pastor,1Animesh Nandi,1Prem Gurnani,1Owen P. McGuinness,3Hirotaka Chikuda,4Masayuki Yamaguchi,4Hiroshi Kawaguchi,4Iichiro Shimomura,5Yoshiharu Takayama,2Joachim Herz,2C. Ronald Kahn,6Kevin P. Rosenblatt,1Makoto Kuro-o1*
A defect in Klotho gene expression in mice accelerates the degenerationof multiple age-sensitive traits. Here, we show that overexpressionof Klotho in mice extends life span. Klotho protein functionsas a circulating hormone that binds to a cell-surface receptorand represses intracellular signals of insulin and insulin-likegrowth factor 1 (IGF1), an evolutionarily conserved mechanismfor extending life span. Alleviation of aging-like phenotypesin Klotho-deficient mice was observed by perturbing insulinand IGF1 signaling, suggesting that Klotho-mediated inhibitionof insulin and IGF1 signaling contributes to its anti-agingproperties. Klotho protein may function as an anti-aging hormonein mammals.
1 Department of Pathology, University of Texas (UT) Southwestern Medical Center at Dallas, 5323 Harry Hines Bouleuvard, Dallas, TX 75390-9072, USA. 2 Department of Molecular Genetics, University of Texas (UT) Southwestern Medical Center at Dallas, 5323 Harry Hines Bouleuvard, Dallas, TX 75390-9072, USA. 3 Department of Molecular Physiology and Biophysics, Vanderbilt University School of Medicine, 702 Light Hall, Nashville, Tennessee 37232-0615, USA. 4 Department of Sensory and Motor System Medicine, University of Tokyo, 7-3-1 Hongo, Bunkyo, Tokyo 113-8655, Japan. 5 Department of Internal Medicine and Molecular Science, Graduate School of Medicine, Osaka University, 2-2 Yamadaoka, Suita, Osaka 565-0871, Japan. 6 Research Division, Joslin Diabetes Center, Department of Medicine, Harvard Medical School, One Joslin Place, Boston, MA 02215, USA.
Published online 25 August 2005;
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* To whom correspondence should be addressed. E-mail: makoto.kuro-o{at}utsouthwestern.edu
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