Mitophagy is required for brown adipose tissue mitochondrial homeostasis during cold challenge

被引:49
|
作者
Lu, Yuan [1 ,2 ]
Fujioka, Hisashi [3 ]
Joshi, Dinesh [4 ]
Li, Qiaoyuan [5 ]
Sangwung, Panjamaporn [1 ,2 ]
Hsieh, Paishiun [1 ,2 ]
Zhu, Jiyun [6 ]
Torio, Jose [1 ,2 ]
Sweet, David [1 ,2 ]
Wang, Lan [7 ]
Chiu, Shing Yan [4 ]
Croniger, Colleen [7 ]
Liao, Xudong [1 ,2 ]
Jain, Mukesh K. [1 ,2 ]
机构
[1] Case Western Reserve Univ, Sch Med, Dept Med, Cardiovasc Res Inst, Cleveland, OH 44106 USA
[2] Univ Hosp Cleveland Med Ctr, Harrington Heart & Vasc Inst, Cleveland, OH 44106 USA
[3] Case Western Reserve Univ, Electron Microscopy Facil, Cleveland, OH 44106 USA
[4] Univ Wisconsin, Sch Med & Publ Hlth, Dept Neurosci, Madison, WI USA
[5] Beijing Capital Med Univ, Beijing Anzhen Hosp, Dept Cardiol, Beijing, Peoples R China
[6] Illinois Math & Sci Acad, Aurora, IL USA
[7] Case Western Reserve Univ, Sch Med, Dept Nutr, Cleveland, OH USA
来源
SCIENTIFIC REPORTS | 2018年 / 8卷
关键词
ADAPTIVE NONSHIVERING THERMOGENESIS; PARKIN-MEDIATED MITOPHAGY; UNCOUPLING PROTEIN-1; MAMMALIAN HOMOLOGS; ENERGY-EXPENDITURE; AUTOPHAGY; PINK1; ACTIVATION; UCP1; MICE;
D O I
10.1038/s41598-018-26394-5
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
Brown adipose tissue (BAT) is a specialized thermogenic organ in mammals. The ability of BAT mitochondria to generate heat in response to cold-challenge to maintain core body temperature is essential for organismal survival. While cold activated BAT mitochondrial biogenesis is recognized as critical for thermogenic adaptation, the contribution of mitochondrial quality control to this process remains unclear. Here, we show mitophagy is required for brown adipocyte mitochondrial homeostasis during thermogenic adaptation. Mitophagy is significantly increased in BAT from cold-challenged mice (4 degrees C) and in beta-agonist treated brown adipocytes. Blockade of mitophagy compromises brown adipocytes mitochondrial oxidative phosphorylation (OX-PHOS) capacity, as well as BAT mitochondrial integrity. Mechanistically, cold-challenge induction of BAT mitophagy is UCP1-dependent. Furthermore, our results indicate that mitophagy coordinates with mitochondrial biogenesis, maintaining activated BAT mitochondrial homeostasis. Collectively, our in vivo and in vitro findings identify mitophagy as critical for brown adipocyte mitochondrial homeostasis during cold adaptation.
引用
收藏
页数:13
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