Mitochondrial Mg2+ homeostasis decides cellular energy metabolism and vulnerability to stress

被引:108
|
作者
Yamanaka, Ryu [1 ]
Tabata, Sho [2 ]
Shindo, Yutaka [1 ]
Hotta, Kohji [1 ]
Suzuki, Koji [3 ]
Soga, Tomoyoshi [2 ]
Oka, Kotaro [1 ]
机构
[1] Keio Univ, Ctr Biosci & Informat, Sch Fundamental Sci & Technol, Grad Sch Sci & Technol, Yokohama, Kanagawa 2238522, Japan
[2] Keio Univ, Inst Adv Biosci, Tsuruoka, Yamagata 9970052, Japan
[3] Keio Univ, Sch Integrated Design Engn, Grad Sch Sci & Technol, Ctr Sci & Technol Designing Funct, Yokohama, Kanagawa 2238522, Japan
来源
SCIENTIFIC REPORTS | 2016年 / 6卷
关键词
RAT-HEART; MAGNESIUM RELEASE; LIVING CELLS; MEMBRANE; DESIGN; FUSION; PHOSPHORYLATION; IDENTIFICATION; MORPHOLOGY; FISSION;
D O I
10.1038/srep30027
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
Cellular energy production processes are composed of many Mg2+ dependent enzymatic reactions. In fact, dysregulation of Mg2+ homeostasis is involved in various cellular malfunctions and diseases. Recently, mitochondria, energy-producing organelles, have been known as major intracellular Mg2+ stores. Several biological stimuli alter mitochondrial Mg2+ concentration by intracellular redistribution. However, in living cells, whether mitochondrial Mg2+ alteration affect cellular energy metabolism remains unclear. Mg2+ transporter of mitochondrial inner membrane MRS2 is an essential component of mitochondrial Mg2+ uptake system. Here, we comprehensively analyzed intracellular Mg2+ levels and energy metabolism in Mrs2 knockdown (KD) cells using fluorescence imaging and metabolome analysis. Dysregulation of mitochondrial Mg2+ homeostasis disrupted ATP production via shift of mitochondrial energy metabolism and morphology. Moreover, Mrs2 KD sensitized cellular tolerance against cellular stress. These results indicate regulation of mitochondrial Mg2+ via MRS2 critically decides cellular energy status and cell vulnerability via regulation of mitochondrial Mg2+ level in response to physiological stimuli.
引用
收藏
页数:12
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