Hajnóczky G, Csordás G, Madesh M, Pacher P
Department of Pathology, Anatomy and Cell Biology, Thomas Jefferson University, Philadelphia, PA 19107, USA.
J Physiol. 2000 Nov 15;529 Pt 1(Pt 1):69-81. doi: 10.1111/j.1469-7793.2000.00069.x.
Growing evidence suggests that propagation of cytosolic [Ca2+] ([Ca2+]c) spikes and oscillations to the mitochondria is important for the control of fundamental cellular functions. Delivery of [Ca2+]c spikes to the mitochondria may utilize activation of the mitochondrial Ca2+ uptake sites by the large local [Ca2+]c rise occurring in the vicinity of activated sarco-endoplasmic reticulum (SR/ER) Ca2+ release channels. Although direct measurement of the local [Ca2+]c sensed by the mitochondria has been difficult, recent studies shed some light onto the molecular mechanism of local Ca2+ communication between SR/ER and mitochondria. Subdomains of the SR/ER are in close contact with mitochondria and display a concentration of Ca2+ release sites, providing the conditions for an effective delivery of released Ca2+ to the mitochondrial targets. Furthermore, many functional properties of the signalling between SR/ER Ca2+ release sites and mitochondrial Ca2+ uptake sites, including transient microdomains of high [Ca2+], saturation of mitochondrial Ca2+ uptake sites by released Ca2+, connection of multiple release sites to each uptake site and quantal transmission, are analogous to the features of the coupling between neurotransmitter release sites and postsynaptic receptors in synaptic transmission. As such, Ca2+ signal transmission between SR/ER and mitochondria may utilize discrete communication sites and a closely related functional architecture to that used for synaptic signal propagation between cells.
越来越多的证据表明,胞质[Ca2+]([Ca2+]c)尖峰和振荡向线粒体的传播对于控制基本细胞功能很重要。[Ca2+]c尖峰向线粒体的传递可能利用激活的肌浆网/内质网(SR/ER)Ca2+释放通道附近局部[Ca2+]c大幅升高对线粒体Ca2+摄取位点的激活。尽管直接测量线粒体感知的局部[Ca2+]c一直很困难,但最近的研究对SR/ER与线粒体之间局部Ca2+通讯的分子机制有所揭示。SR/ER的亚结构域与线粒体紧密接触,并显示出Ca2+释放位点的聚集,为将释放的Ca2+有效传递到线粒体靶点提供了条件。此外,SR/ER Ca2+释放位点与线粒体Ca2+摄取位点之间信号传导的许多功能特性,包括高[Ca2+]的瞬时微区、释放的Ca2+使线粒体Ca2+摄取位点饱和、多个释放位点与每个摄取位点的连接以及量子传递,类似于突触传递中神经递质释放位点与突触后受体之间耦合的特征。因此,SR/ER与线粒体之间的Ca2+信号传递可能利用离散的通讯位点以及与细胞间突触信号传播所使用的紧密相关的功能结构。