缺血性视网膜病变中小胶质细胞和Müller细胞相互作用的机制

Q4 Medicine
Shuang Gao
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引用次数: 0

摘要

缺血性视网膜病变导致多发性病变,如微血管损伤、炎症和新生血管形成,是视力损伤的主要原因。在这些病理变化中,视网膜胶质细胞在视网膜病变的发展中是不可忽视的。它们构成了一个高度通用的群体,与各种细胞相互作用,以维持体内平衡并限制疾病。因此,胶质细胞活化和胶质增生是几乎所有形式的视网膜疾病的普遍反应。小胶质细胞和穆勒细胞都是视网膜固有的主要神经胶质细胞,它们之间关系密切,这意味着它们可以相互影响,共同作用,甚至变得相互依赖。它们表现出形态和功能变化,通过不同的反应对视网膜损伤程度产生影响,神经胶质细胞介导的反应不仅对疾病进展过程很重要,而且对维持神经元和光感受器的存活也很重要。因此,确定小胶质细胞和穆勒细胞之间通讯的机制可以开发出更具选择性的治疗靶点,具有巨大的临床应用潜力。关键词:小胶质细胞;穆勒细胞;评审;缺血性视网膜病变
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The mechanisms for mutual interactions between microglial cell and Müller cell in ischemic retinopathy
Ischemic retinopathy, resulting in multiple lesions like microvasculature damage, inflammation and neovascularization, is a major contributor of vision damage. In these pathological changes, retinal glia cannot be ignored in the development of retinopathy. They constitute a highly versatile population that interacts with various cells to maintain homeostasis and limit disease. Therefore, glial activation and gliosis are strikingly ubiquitous responses to almost every form of retinal disease. Both of microglial cells and Muller cells are major intrinsic retinal glial cells and they are in close relationship, which means they can influence each other, make joint action or even become interdependent. They exhibit morphological and functional changes to have an impact on degree of retinal injury through different responses, which mediated by glial cells are important not only for course of disease progression, but also for the maintenance of neuronal and photoreceptor survival. Thus, defining the mechanisms that underlie communications between microglial cells and Muller cells could enable the development of more selective therapeutic targets, with great potential clinical applications. Key words: Microglia; Muller cell; Review; Ischemic retinopathy
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来源期刊
中华眼底病杂志
中华眼底病杂志 Medicine-Ophthalmology
CiteScore
0.40
自引率
0.00%
发文量
5383
期刊介绍: Chinese Journal of Ocular Fundus Diseases is the only scientific journal in my country that focuses on reporting fundus diseases. Its purpose is to combine clinical and basic research, and to give equal importance to improvement and popularization. It comprehensively reflects the leading clinical and basic research results of fundus disease disciplines in my country; cultivates professional talents in fundus disease, promotes the development of fundus disease disciplines in my country; and promotes academic exchanges on fundus disease at home and abroad. The coverage includes clinical and basic research results of posterior segment diseases such as retina, uveal tract, vitreous body, visual pathway, and internal eye diseases related to systemic diseases. The readers are medical workers and researchers related to clinical and basic research of fundus diseases. According to the journal retrieval report of the Chinese Institute of Scientific and Technological Information, the comprehensive ranking impact factor and total citation frequency of the Chinese Journal of Ocular Fundus Diseases have been among the best in the disciplines of ophthalmology, otolaryngology, and ophthalmology in my country for many years. The papers published have been included in many important databases at home and abroad, such as Scopus, Peking University Core, and China Science Citation Database (CSCD).
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