RETRACTED: Increased muscle PGC-1α expression protects from sarcopenia and metabolic disease during aging(Retracted article. See vol.113,pg.E8502,2016)

被引:490
作者
Wenz, Tina [1 ]
Rossi, Susana G. [2 ]
Rotundo, Richard L. [2 ]
Spiegelman, Bruce M. [3 ]
Moraes, Carlos T. [1 ,2 ]
机构
[1] Univ Miami, Sch Med, Dept Neurol, Miami, FL 33136 USA
[2] Univ Miami, Sch Med, Dept Cell Biol & Anat, Miami, FL 33136 USA
[3] Harvard Univ, Sch Med, Dana Farber Canc Inst, Dept Cell Biol, Boston, MA 02115 USA
关键词
mitochondria; PGC-1; alpha; MITOCHONDRIAL-FUNCTION; SKELETAL-MUSCLE; INFLAMMATORY MARKERS; INSULIN SENSITIVITY; CALORIE RESTRICTION; PPAR-GAMMA; AGE; ACTIVATION; IMPROVES; GENE;
D O I
10.1073/pnas.0911570106
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Aging is a major risk factor for metabolic disease and loss of skeletal muscle mass and strength, a condition known as sarcopenia. Both conditions present a major health burden to the elderly population. Here, we analyzed the effect of mildly increased PGC-1 alpha expression in skeletal muscle during aging. We found that transgenic MCK-PGC-1 alpha animals had preserved mitochondrial function, neuromuscular junctions, and muscle integrity during aging. Increased PGC-1 alpha levels in skeletal muscle prevented muscle wasting by reducing apoptosis, autophagy, and proteasome degradation. The preservation of muscle integrity and function in MCK-PGC-1 alpha animals resulted in significantly improved whole-body health; both the loss of bone mineral density and the increase of systemic chronic inflammation, observed during normal aging, were prevented. Importantly, MCK-PGC-1 alpha animals also showed improved metabolic responses as evident by increased insulin sensitivity and insulin signaling in aged mice. Our results highlight the importance of intact muscle function and metabolism for whole-body homeostasis and indicate that modulation of PGC-1 alpha levels in skeletal muscle presents an avenue for the prevention and treatment of a group of age-related disorders.
引用
收藏
页码:20405 / 20410
页数:6
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