Mitochondrial matrix Ca2+ as an intrinsic signal regulating mitochondrial motility in axons

被引:127
作者
Chang, Karen T. [1 ,2 ]
Niescier, Robert F. [3 ]
Min, Kyung-Tai [3 ]
机构
[1] Univ So Calif, Zilkha Neurogenet Inst, Los Angeles, CA 90033 USA
[2] Univ So Calif, Dept Cell & Neurobiol, Los Angeles, CA 90033 USA
[3] Indiana Univ, Dept Biol, Bloomington, IN 47405 USA
基金
美国国家卫生研究院;
关键词
FLUORESCENT PROTEIN; CALCIUM UNIPORTER; GROWTH-FACTOR; TRANSPORT; HOMEOSTASIS; INHIBITOR; MECHANISM; MOVEMENT; SB202190; NEURONS;
D O I
10.1073/pnas.1106862108
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
070301 [无机化学]; 070403 [天体物理学]; 070507 [自然资源与国土空间规划学]; 090105 [作物生产系统与生态工程];
摘要
The proper distribution of mitochondria is particularly vital for neurons because of their polarized structure and high energy demand. Mitochondria in axons constantly move in response to physiological needs, but signals that regulate mitochondrial movement are not well understood. Aside from producing ATP, Ca2+ buffering is another main function of mitochondria. Activities of many enzymes in mitochondria are also Ca2+-dependent, suggesting that intramitochondrial Ca2+ concentration is important for mitochondrial functions. Here, we report that mitochondrial motility in axons is actively regulated by mitochondrial matrix Ca2+. Ca2+ entry through the mitochondrial Ca2+ uniporter modulates mitochondrial transport, and mitochondrial Ca2+ content correlates inversely with the speed of mitochondrial movement. Furthermore, the miro1 protein plays a role in Ca2+ uptake into the mitochondria, which subsequently affects mitochondrial movement.
引用
收藏
页码:15456 / 15461
页数:6
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