抗nmda受体脑炎:机制研究综述。

International journal of physiology, pathophysiology and pharmacology Pub Date : 2021-02-15 eCollection Date: 2021-01-01
Yue-Qiao Huang, Huangui Xiong
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引用次数: 0

摘要

NMDA受体(NMDARs)是由谷氨酸控制的离子通道,谷氨酸是中枢神经系统中主要的兴奋性神经递质。抗nmda受体(抗NMDAR)脑炎是一种自身免疫性疾病,其特征是存在针对NMDAR GluN1亚基的自身抗体。在这里,我们简要回顾了目前对抗nmdar脑炎发病机制的了解进展。自身抗体结合并交联内源性NMDARs,破坏NMDARs与受体酪氨酸激酶EphB2的相互作用,导致NMDARs内化和功能降低。NMDARs功能低下导致长期增强功能受损,学习和记忆缺陷,导致抑郁样行为的发展,并降低癫痫发作的阈值。抗nmdar脑炎主动免疫模型的最新发展为了解炎症过程提供了新的思路,并为进一步的研究铺平了道路,从而可能导致更好的治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Anti-NMDA receptor encephalitis: a review of mechanistic studies.

NMDA receptors (NMDARs) are ion channels gated by glutamate, the major excitatory neurotransmitter in the central nervous system. Anti-NMDA receptor (anti-NMDAR) encephalitis is an autoimmune disease characterized by the presence of autoantibodies against the NMDAR GluN1 subunit. Here we briefly review current advances in the understanding of the mechanisms underlying the pathogenesis of anti-NMDAR encephalitis. The autoantibodies bind to and cross-link the endogenous NMDARs, disrupt the interaction of NMDARs with receptor tyrosine kinase EphB2 leading to internalization and reduced function of NMDARs. Hypofunction of the NMDARs results in impairment in long-term potentiation and deficit in learning and memory, leads to development of depression-like behavior, and lowers the threshold for seizures. Recent development of active immunization models of anti-NMDAR encephalitis provides insight into the inflammation process and paves the way for further studies that may lead to better treatment.

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