Literature DB >> 29781176

Autophagy and mitophagy flux in young and aged skeletal muscle following chronic contractile activity.

Heather N Carter1, Yuho Kim1, Avigail T Erlich1, Dorrin Zarrin-Khat1,2, David A Hood1.   

Abstract

KEY POINTS: A healthy mitochondrial pool is dependent on the removal of dysfunctional organelles via mitophagy, but little is known about how mitophagy is altered with ageing and chronic exercise. Chronic contractile activity (CCA) is a standardized exercise model that can elicit mitochondrial adaptations in both young and aged muscle, albeit to a lesser degree in the aged group. Assessment of mitophagy flux revealed enhanced targeting of mitochondria for degradation in aged muscle, in contrast to previous theories. Mitophagy flux was significantly reduced as an adaptation to CCA suggesting that an improvement in organelle quality reduces the need for mitochondrial turnover. CCA enhances lysosomal capacity and may ameliorate lysosomal dysfunction in aged muscle. ABSTRACT: Skeletal muscle exhibits deficits in mitochondrial quality with age. Central to the maintenance of a healthy mitochondrial pool is the removal of dysfunctional organelles via mitophagy. Little is known on how mitophagy is altered with ageing and chronic exercise. We assessed mitophagy flux using colchicine treatment in vivo following chronic contractile activity (CCA) of muscle in young and aged rats. CCA evoked mitochondrial biogenesis in young muscle, with an attenuated response in aged muscle. Mitophagy flux was higher in aged muscle and was correlated with the enhanced expression of mitophagy receptors and upstream transcriptional regulators. CCA decreased mitophagy flux in both age groups, suggesting an improvement in organelle quality. CCA also reduced the exaggerated expression of TFEB evident in aged muscle, which may be promoting the age-induced increase in lysosomal markers. Thus, aged muscle possesses an elevated drive for autophagy and mitophagy which may contribute to the decline in organelle content observed with age, but which may serve to maintain mitochondrial quality. CCA improves organelle integrity and reduces mitophagy, illustrating that chronic exercise is a modality to improve muscle quality in aged populations.
© 2018 The Authors. The Journal of Physiology © 2018 The Physiological Society.

Entities:  

Keywords:  aging; exercise; mitochondria

Mesh:

Substances:

Year:  2018        PMID: 29781176      PMCID: PMC6092298          DOI: 10.1113/JP275998

Source DB:  PubMed          Journal:  J Physiol        ISSN: 0022-3751            Impact factor:   5.182


  89 in total

Review 1.  The mitochondrial-lysosomal axis theory of aging: accumulation of damaged mitochondria as a result of imperfect autophagocytosis.

Authors:  Ulf T Brunk; Alexei Terman
Journal:  Eur J Biochem       Date:  2002-04

2.  Elevated energy coupling and aerobic capacity improves exercise performance in endurance-trained elderly subjects.

Authors:  Kevin E Conley; Sharon A Jubrias; M Elaine Cress; Peter C Esselman
Journal:  Exp Physiol       Date:  2012-11-30       Impact factor: 2.969

3.  p53 mediates autophagy and cell death by a mechanism contingent on Bnip3.

Authors:  Erika Yan Wang; Hongying Gang; Yaron Aviv; Rimpy Dhingra; Victoria Margulets; Lorrie A Kirshenbaum
Journal:  Hypertension       Date:  2013-05-06       Impact factor: 10.190

4.  Ubiquitin is phosphorylated by PINK1 to activate parkin.

Authors:  Fumika Koyano; Kei Okatsu; Hidetaka Kosako; Yasushi Tamura; Etsu Go; Mayumi Kimura; Yoko Kimura; Hikaru Tsuchiya; Hidehito Yoshihara; Takatsugu Hirokawa; Toshiya Endo; Edward A Fon; Jean-François Trempe; Yasushi Saeki; Keiji Tanaka; Noriyuki Matsuda
Journal:  Nature       Date:  2014-06-04       Impact factor: 49.962

Review 5.  Autophagy and aging.

Authors:  David C Rubinsztein; Guillermo Mariño; Guido Kroemer
Journal:  Cell       Date:  2011-09-02       Impact factor: 41.582

6.  Age-dependent upregulation of p53 and cytochrome c release and susceptibility to apoptosis in skeletal muscle fiber of aged rats: role of carnitine and lipoic acid.

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Journal:  Free Radic Biol Med       Date:  2007-09-14       Impact factor: 7.376

7.  Phosphorylation of OPTN by TBK1 enhances its binding to Ub chains and promotes selective autophagy of damaged mitochondria.

Authors:  Benjamin Richter; Danielle A Sliter; Lina Herhaus; Alexandra Stolz; Chunxin Wang; Petra Beli; Gabriele Zaffagnini; Philipp Wild; Sascha Martens; Sebastian A Wagner; Richard J Youle; Ivan Dikic
Journal:  Proc Natl Acad Sci U S A       Date:  2016-03-30       Impact factor: 11.205

8.  PGC-1α modulates denervation-induced mitophagy in skeletal muscle.

Authors:  Anna Vainshtein; Eric Ma Desjardins; Andrea Armani; Marco Sandri; David A Hood
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9.  Mitofusin 1 and mitofusin 2 are ubiquitinated in a PINK1/parkin-dependent manner upon induction of mitophagy.

Authors:  Matthew E Gegg; J Mark Cooper; Kai-Yin Chau; Manuel Rojo; Anthony H V Schapira; Jan-Willem Taanman
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