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Exercise-induced BCL2-regulated autophagy is required for muscle glucose homeostasis 总被引:3,自引:0,他引:3
He C Bassik MC Moresi V Sun K Wei Y Zou Z An Z Loh J Fisher J Sun Q Korsmeyer S Packer M May HI Hill JA Virgin HW Gilpin C Xiao G Bassel-Duby R Scherer PE Levine B 《Nature》2012,481(7382):511-515
Exercise has beneficial effects on human health, including protection against metabolic disorders such as diabetes. However, the cellular mechanisms underlying these effects are incompletely understood. The lysosomal degradation pathway, autophagy, is an intracellular recycling system that functions during basal conditions in organelle and protein quality control. During stress, increased levels of autophagy permit cells to adapt to changing nutritional and energy demands through protein catabolism. Moreover, in animal models, autophagy protects against diseases such as cancer, neurodegenerative disorders, infections, inflammatory diseases, ageing and insulin resistance. Here we show that acute exercise induces autophagy in skeletal and cardiac muscle of fed mice. To investigate the role of exercise-mediated autophagy in vivo, we generated mutant mice that show normal levels of basal autophagy but are deficient in stimulus (exercise- or starvation)-induced autophagy. These mice (termed BCL2 AAA mice) contain knock-in mutations in BCL2 phosphorylation sites (Thr69Ala, Ser70Ala and Ser84Ala) that prevent stimulus-induced disruption of the BCL2-beclin-1 complex and autophagy activation. BCL2 AAA mice show decreased endurance and altered glucose metabolism during acute exercise, as well as impaired chronic exercise-mediated protection against high-fat-diet-induced glucose intolerance. Thus, exercise induces autophagy, BCL2 is a crucial regulator of exercise- (and starvation)-induced autophagy in vivo, and autophagy induction may contribute to the beneficial metabolic effects of exercise. 相似文献
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Mutations in the endosomal ESCRTIII-complex subunit CHMP2B in frontotemporal dementia 总被引:21,自引:0,他引:21
Skibinski G Parkinson NJ Brown JM Chakrabarti L Lloyd SL Hummerich H Nielsen JE Hodges JR Spillantini MG Thusgaard T Brandner S Brun A Rossor MN Gade A Johannsen P Sørensen SA Gydesen S Fisher EM Collinge J 《Nature genetics》2005,37(8):806-808
We have previously reported a large Danish pedigree with autosomal dominant frontotemporal dementia (FTD) linked to chromosome 3 (FTD3). Here we identify a mutation in CHMP2B, encoding a component of the endosomal ESCRTIII complex, and show that it results in aberrant mRNA splicing in tissue samples from affected members of this family. We also describe an additional missense mutation in an unrelated individual with FTD. Aberration in the endosomal ESCRTIII complex may result in FTD and neurodegenerative disease. 相似文献
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Y. Lass S. Akselrod B. Gavish S. Cohen A. Fisher 《Cellular and molecular life sciences : CMLS》1979,35(5):650-652
Summary Time course measurements of the action of muscarinic antagonists were performed in the spontaneously beating carp atrium. Several high affinity drugs, which embody the quinuclidine structure were examined. The structural flexibility of these molecules was reflected in the dissociation of the drugs from the muscarinic receptor. The dissociation of rigid drugs was very much prolonged as compared to flexible drugs of the same affinity.We thank Prof. S. Lifson for helpful discussion and Mrs M. Bendikovsky for technical assistance. This work was supported by a USA-Israel Binational Science Foundation (BSF-Jerusalem) grant to Y. Lass. 相似文献