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小胶质细胞中的TRPM2通道作为与一系列中枢神经系统病理相关的神经炎症中的新角色。

TRPM2 Channel in Microglia as a New Player in Neuroinflammation Associated With a Spectrum of Central Nervous System Pathologies.

作者信息

Malko Philippa, Syed Mortadza Sharifah A, McWilliam Joseph, Jiang Lin-Hua

机构信息

School of Biomedical Sciences, Faculty of Biological Sciences, University of Leeds, Leeds, United Kingdom.

Department of Biochemistry, Universiti Putra Malaysia, Seri Kembangan, Malaysia.

出版信息

Front Pharmacol. 2019 Mar 12;10:239. doi: 10.3389/fphar.2019.00239. eCollection 2019.

DOI:10.3389/fphar.2019.00239
PMID:30914955
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6423084/
Abstract

Microglial cells in the central nervous system (CNS) are crucial in maintaining a healthy environment for neurons to function properly. However, aberrant microglial cell activation can lead to excessive generation of neurotoxic proinflammatory mediators and neuroinflammation, which represents a contributing factor in a wide spectrum of CNS pathologies, including ischemic stroke, traumatic brain damage, Alzheimer's disease, Parkinson's disease, multiple sclerosis, psychiatric disorders, autism spectrum disorders, and chronic neuropathic pain. Oxidative stress is a salient and common feature of these conditions and has been strongly implicated in microglial cell activation and neuroinflammation. The transient receptor potential melastatin-related 2 (TRPM2) channel, an oxidative stress-sensitive calcium-permeable cationic channel, is highly expressed in microglial cells. In this review, we examine the recent studies that provide evidence to support an important role for the TRPM2 channel, particularly TRPM2-mediated Ca signaling, in mediating microglial cell activation, generation of proinflammatory mediators and neuroinflammation, which are of relevance to CNS pathologies. These findings lead to a growing interest in the TRPM2 channel, a new player in neuroinflammation, as a novel therapeutic target for CNS diseases.

摘要

中枢神经系统(CNS)中的小胶质细胞对于维持神经元正常运作的健康环境至关重要。然而,小胶质细胞的异常激活会导致神经毒性促炎介质过度产生和神经炎症,这是包括缺血性中风、创伤性脑损伤、阿尔茨海默病、帕金森病、多发性硬化症、精神疾病、自闭症谱系障碍和慢性神经性疼痛在内的多种中枢神经系统疾病的一个促成因素。氧化应激是这些病症的一个显著且常见的特征,并且与小胶质细胞激活和神经炎症密切相关。瞬时受体电位褪黑素相关2(TRPM2)通道是一种对氧化应激敏感的钙通透性阳离子通道,在小胶质细胞中高度表达。在这篇综述中,我们研究了最近的一些研究,这些研究提供了证据支持TRPM2通道,特别是TRPM2介导的钙信号传导,在介导小胶质细胞激活、促炎介质产生和神经炎症中发挥重要作用,而这些与中枢神经系统疾病相关。这些发现引发了人们对TRPM2通道(神经炎症中的一个新参与者)作为中枢神经系统疾病新型治疗靶点的兴趣日益浓厚。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/132d/6423084/b81ebd8754a8/fphar-10-00239-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/132d/6423084/1d2b2a437de6/fphar-10-00239-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/132d/6423084/d49b5feac551/fphar-10-00239-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/132d/6423084/b81ebd8754a8/fphar-10-00239-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/132d/6423084/1d2b2a437de6/fphar-10-00239-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/132d/6423084/d49b5feac551/fphar-10-00239-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/132d/6423084/b81ebd8754a8/fphar-10-00239-g003.jpg

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