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KA-AMPA 门控型谷氨酸受体通道的钙离子通透性取决于亚基组成。

Ca2+ permeability of KA-AMPA--gated glutamate receptor channels depends on subunit composition.

作者信息

Hollmann M, Hartley M, Heinemann S

机构信息

Molecular Neurobiology Laboratory, Salk Institute for Biological Studies, La Jolla, CA 92037.

出版信息

Science. 1991 May 10;252(5007):851-3. doi: 10.1126/science.1709304.

Abstract

NMDA (N-methyl-D-aspartate) receptors and non-NMDA receptors represent the two major classes of ion channel-linked glutamate receptors. Unlike the NMDA receptor channels, non-NMDA receptor channels have usually been thought to conduct monovalent cations only. Non-NMDA receptor ion channels that can be gated by kainic acid (KA) and alpha-amino-3-hydroxy-5-methyl-4-isoxazole propionic acid (AMPA) are formed by the glutamate receptor subunits GluR1, GluR2, and GluR3. These subunits were expressed in various combinations in Xenopus oocytes so that their permeability to divalent cations could be studied. At physiological resting potentials, KA and AMPA elicited inward calcium currents in oocytes expressing GluR1, GluR3, and GluR1 plus GluR3. In contrast, oocytes expressing GluR1 plus GluR2 or GluR3 plus GluR2 showed no such permeability. Thus, in neurons expressing certain KA-AMPA receptor subunits, glutamate may trigger calcium-dependent intracellular events by activating non-NMDA receptors.

摘要

N-甲基-D-天冬氨酸(NMDA)受体和非NMDA受体是离子通道偶联型谷氨酸受体的两大主要类型。与NMDA受体通道不同,非NMDA受体通道通常被认为仅传导单价阳离子。可被海人酸(KA)和α-氨基-3-羟基-5-甲基-4-异恶唑丙酸(AMPA)门控的非NMDA受体离子通道由谷氨酸受体亚基GluR1、GluR2和GluR3构成。这些亚基在非洲爪蟾卵母细胞中以各种组合形式表达,以便研究它们对二价阳离子的通透性。在生理静息电位下,KA和AMPA在表达GluR1、GluR3以及GluR1加GluR3的卵母细胞中引发内向钙电流。相比之下,表达GluR1加GluR2或GluR3加GluR2的卵母细胞则未表现出这种通透性。因此,在表达某些KA-AMPA受体亚基的神经元中,谷氨酸可能通过激活非NMDA受体触发钙依赖性细胞内事件。

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