Blackstone C, Sheng M
Department of Neurology, Massachusetts General Hospital and Harvard Medical School, Boston 02114, USA.
Cell Calcium. 1999 Nov;26(5):181-92. doi: 10.1054/ceca.1999.0071.
Over the last several years, a number of optical imaging, physiological, and molecular studies have clarified the mechanisms underlying differential calcium signaling in the postsynaptic neuron. These studies have revealed the existence of membrane-associated calcium microdomains, which are often specifically coupled to distinct protein signaling pathways. In this review, we discuss how these signaling microdomains are organized and regulated, emphasizing the structural and molecular features of synaptic protein complexes containing the metabotropic and N-methyl-D-aspartate (NMDA) glutamate receptors and the L-type voltage-dependent calcium channels (VDCCs). We conclude with a discussion of how these different signaling complexes may interact with one another, relationships which may be important in orchestrating the complex calcium signaling underlying developmental and activity-dependent changes in synaptic function.
在过去几年中,大量的光学成像、生理学和分子研究已经阐明了突触后神经元中差异性钙信号传导的潜在机制。这些研究揭示了膜相关钙微区的存在,这些微区通常与不同的蛋白质信号通路特异性偶联。在本综述中,我们讨论了这些信号微区是如何组织和调控的,重点强调了包含代谢型和N-甲基-D-天冬氨酸(NMDA)谷氨酸受体以及L型电压依赖性钙通道(VDCCs)的突触蛋白复合物的结构和分子特征。我们最后讨论了这些不同的信号复合物可能如何相互作用,这些关系可能在协调突触功能发育和活动依赖性变化所涉及的复杂钙信号传导方面具有重要意义。