A persistent level of Cisd2 extends healthy lifespan and delays aging in mice

Chia-Yu Wu(National Yang Ming Chiao Tung University), Yi‐Fan Chen(National Health Research Institutes), Chih‐Hao Wang, Cheng-Heng Kao(Chang Gung University), Hui-Wen Zhuang, Chih‐Cheng Chen(Institute of Biomedical Sciences, Academia Sinica), Liang‐Kung Chen(Taipei Veterans General Hospital), Ralph Kirby, Yau‐Huei Wei(Mackay Medical University), Shih-Feng Tsai(National Health Research Institutes), Ting‐Fen Tsai(National Yang Ming Chiao Tung University)
Human Molecular Genetics
June 1, 2012
Cited by 98Open Access
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Abstract

The CISD2 gene, which is an evolutionarily conserved novel gene, encodes a transmembrane protein primarily associated with the mitochondrial outer membrane. Significantly, the CISD2 gene is located within the candidate region on chromosome 4q where a genetic component for human longevity has been mapped. Previously, we have shown that Cisd2 deficiency shortens lifespan resulting in premature aging in mice. Additionally, an age-dependent decrease in Cisd2 expression has been detected during normal aging. In this study, we demonstrate that a persistent level of Cisd2 achieved by transgenic expression in mice extends their median and maximum lifespan without any apparent deleterious side effects. Cisd2 also ameliorates age-associated degeneration of the skin, skeletal muscles and neurons. Moreover, Cisd2 protects mitochondria from age-associated damage and functional decline as well as attenuating the age-associated reduction in whole-body energy metabolism. These results suggest that Cisd2 is a fundamentally important regulator of lifespan and provide an experimental basis for exploring the candidacy of CISD2 in human longevity.


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