Michaelis E K, Michaelis M L
Department of Pharmacology and Toxicology, University of Kansas, Lawrence 66047.
Neurochem Res. 1992 Jan;17(1):29-34. doi: 10.1007/BF00966862.
N-Methyl-D-aspartate (NMDA) and L-glutamate activate membrane receptors that produce substantial permeation of Na+, K+ and Ca2+ through the neuronal membrane. These ionic fluxes are intimately linked to processes that regulate neuronal survival, growth and differentiation. Intracellular free Ca2+ concentrations are thought to be particularly important determinants of the vulnerability of neurons to excessive excitatory stimulation produced through activation of NMDA receptors. In order to understand the molecular events involved in both NMDA receptor activation and regulation of intracellular Ca2+ levels, we have purified and reconstituted the protein complexes that form the NMDA/glutamate receptors in rat brain synaptic membranes and those that constitute the Na(+)-Ca2+ antiporters in bovine brain synaptic membrane. The molecular properties of these protein complexes are described, and information from the most recent studies of exploration of the molecular structures of these receptors and transport carriers is summarized.
N-甲基-D-天冬氨酸(NMDA)和L-谷氨酸激活膜受体,这些受体可使Na+、K+和Ca2+大量透过神经元膜。这些离子通量与调节神经元存活、生长和分化的过程密切相关。细胞内游离Ca2+浓度被认为是神经元对通过NMDA受体激活产生的过度兴奋性刺激易感性的特别重要的决定因素。为了了解NMDA受体激活和细胞内Ca2+水平调节所涉及的分子事件,我们已经纯化并重组了大鼠脑突触膜中形成NMDA/谷氨酸受体的蛋白质复合物以及牛脑突触膜中构成Na(+)-Ca2+反向转运体的蛋白质复合物。本文描述了这些蛋白质复合物的分子特性,并总结了对这些受体和转运载体分子结构探索的最新研究信息。