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PMID: 24994533 已发表 · ppublish 英语

The destiny of Ca(2+) released by mitochondria.

The journal of physiological sciences : JPS ·第 65 卷 ·第 1 期 ·2015-09-15

Takeuchi Ayako, Kim Bongju, Matsuoka Satoshi

摘要

Mitochondrial Ca(2+) is known to regulate diverse cellular functions, for example energy production and cell death, by modulating mitochondrial dehydrogenases, inducing production of reactive oxygen species, and opening mitochondrial permeability transition pores. In addition to the action of Ca(2+) within mitochondria, Ca(2+) released from mitochondria is also important in a variety of cellular functions. In the last 5 years, the molecules responsible for mitochondrial Ca(2+) dynamics have been identified: a mitochondrial Ca(2+) uniporter (MCU), a mitochondrial Na(+)-Ca(2+) exchanger (NCLX), and a candidate for a mitochondrial H(+)-Ca(2+) exchanger (Letm1). In this review, we focus on the mitochondrial Ca(2+) release system, and discuss its physiological and pathophysiological significance. Accumulating evidence suggests that the mitochondrial Ca(2+) release system is not only crucial in maintaining mitochondrial Ca(2+) homeostasis but also participates in the Ca(2+) crosstalk between mitochondria and the plasma membrane and between mitochondria and the endoplasmic/sarcoplasmic reticulum.

文献信息
期刊
The journal of physiological sciences : JPS
期刊简称
J Physiol Sci
发表日期
2015-09-15
收录日期
2014-12-26
更新日期
2014-12-31
语言
英语
国家/地区
Japan
NLM ID
101262417
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