Cegielski Victoria, Chakrabarty Rohan, Ding Shinghua, Wacker Michael J, Monaghan-Nichols Paula, Chu Xiang-Ping
Department of Biomedical Sciences, School of Medicine, University of Missouri-Kansas City, Kansas City, MO 64108, USA.
Department of Biomedical, Biological and Chemical Engineering, University of Missouri-Columbia, Columbia, MO 65211, USA.
Membranes (Basel). 2022 Jan 20;12(2):119. doi: 10.3390/membranes12020119.
Acid-sensing ion channels (ASICs) are proton-gated cation channels and key mediators of responses to neuronal injury. ASICs exhibit unique patterns of distribution in the brain, with high expression in neurons and low expression in glial cells. While there has been a lot of focus on ASIC in neurons, less is known about the roles of ASICs in glial cells. ASIC1a is expressed in astrocytes and might contribute to synaptic transmission and long-term potentiation. In oligodendrocytes, constitutive activation of ASIC1a participates in demyelinating diseases. ASIC1a, ASIC2a, and ASIC3, found in microglial cells, could mediate the inflammatory response. Under pathological conditions, ASIC dysregulation in glial cells can contribute to disease states. For example, activation of astrocytic ASIC1a may worsen neurodegeneration and glioma staging, activation of microglial ASIC1a and ASIC2a may perpetuate ischemia and inflammation, while oligodendrocytic ASIC1a might be involved in multiple sclerosis. This review concentrates on the unique ASIC components in each of the glial cells and integrates these glial-specific ASICs with their physiological and pathological conditions. Such knowledge provides promising evidence for targeting of ASICs in individual glial cells as a therapeutic strategy for a diverse range of conditions.
酸敏感离子通道(ASICs)是质子门控阳离子通道,也是神经元损伤反应的关键介质。ASICs在大脑中呈现出独特的分布模式,在神经元中高表达,在胶质细胞中低表达。虽然人们对神经元中的ASICs给予了很多关注,但对ASICs在胶质细胞中的作用了解较少。ASIC1a在星形胶质细胞中表达,可能有助于突触传递和长时程增强。在少突胶质细胞中,ASIC1a的组成性激活参与脱髓鞘疾病。在小胶质细胞中发现的ASIC1a、ASIC2a和ASIC3可介导炎症反应。在病理条件下,胶质细胞中ASIC的失调可导致疾病状态。例如,星形胶质细胞ASIC1a的激活可能会加重神经退行性变和胶质瘤分期,小胶质细胞ASIC1a和ASIC2a的激活可能会使缺血和炎症持续存在,而少突胶质细胞ASIC1a可能与多发性硬化症有关。这篇综述集中于每种胶质细胞中独特的ASIC成分,并将这些胶质细胞特异性的ASICs与其生理和病理状况相结合。这些知识为将单个胶质细胞中的ASICs作为多种疾病的治疗策略提供了有前景的证据。