Gunter T E, Pfeiffer D R
Department of Biophysics, University of Rochester, New York 14642.
Am J Physiol. 1990 May;258(5 Pt 1):C755-86. doi: 10.1152/ajpcell.1990.258.5.C755.
It has been firmly established that the rapid uptake of Ca2+ by mitochondria from a wide range of sources is mediated by a uniporter which permits transport of the ion down its electrochemical gradient. Several mechanisms of Ca2+ efflux from mitochondria have also been extensively discussed in the literature. Energized mitochondria must expend a significant amount of energy to transport Ca2+ against its electrochemical gradient from the matrix space to the external space. Two separate mechanisms have been found to mediate this outward transport: a Ca2+/nNa+ exchanger and a Na(+)-independent efflux mechanism. These efflux mechanisms are considered from the perspective of available energy. In addition, a reversible Ca2(+)-induced increase in inner membrane permeability can also occur. The induction of this permeability transition is characterized by swelling of the mitochondria, leakiness to small ions such as K+, Mg2+, and Ca2+, and loss of the mitochondrial membrane potential. It has been suggested that the permeability transition and its reversal may also function as a mitochondrial Ca2+ efflux mechanism under some conditions. The characteristics of each of these mechanisms are discussed, as well as their possible physiological functions.
业已明确证实,线粒体从多种来源快速摄取Ca2+是由单向转运体介导的,该转运体允许离子沿其电化学梯度进行运输。文献中也广泛讨论了几种线粒体Ca2+外流机制。活跃的线粒体必须消耗大量能量,才能将Ca2+逆其电化学梯度从基质空间转运到外部空间。现已发现两种独立的机制介导这种外向运输:一种Ca2+/nNa+交换体和一种不依赖Na+的外流机制。这些外流机制是从可用能量的角度来考虑的。此外,还可能发生可逆的Ca2+诱导的内膜通透性增加。这种通透性转变的诱导表现为线粒体肿胀、对K+、Mg2+和Ca2+等小离子的泄漏以及线粒体膜电位的丧失。有人提出,在某些条件下,通透性转变及其逆转也可能作为一种线粒体Ca2+外流机制发挥作用。本文讨论了每种机制的特点及其可能的生理功能。