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CD68:可能导致炎症和 RPE 细胞营养不良的因素。

CD68: Potential Contributor to Inflammation and RPE Cell Dystrophy.

机构信息

Department of Ophthalmology, Albert Eye Research Institute, Duke University School of Medicine, Durham, NC, USA.

Department of Pathology, Albert Eye Research Institute, Duke University School of Medicine, Durham, NC, USA.

出版信息

Adv Exp Med Biol. 2023;1415:207-213. doi: 10.1007/978-3-031-27681-1_30.

Abstract

Age-related macular degeneration (AMD) is the leading cause of visual impairment in the elderly in developed countries. It is a complex, multifactorial, progressive disease with diverse molecular pathways, including inflammation, regulating its pathogenesis. The myeloid marker CD68 is a protein highly expressed in circulating and tissue macrophages. Recent observations of immune markers in human AMD tissues have varied with some finding ectopic RPE cells in advanced AMD and others noting negligible numbers of CD68-positive cells. Additionally, animal models of retinal degeneration have shown upregulation of CD68, in a protective population of retinal microglia. Herein, we review the potential role of CD68 in regulating RPE health and inflammation in the sub-retinal space and discuss observations on its localization in a mouse model that presents with AMD-like features.

摘要

年龄相关性黄斑变性(AMD)是发达国家老年人视力损害的主要原因。它是一种复杂的、多因素的、进行性疾病,具有多种分子途径,包括炎症,调节其发病机制。髓样标志物 CD68 是一种在循环和组织巨噬细胞中高度表达的蛋白质。最近在人类 AMD 组织中观察到的免疫标志物各不相同,一些发现晚期 AMD 中有异位 RPE 细胞,而另一些则发现 CD68 阳性细胞数量可忽略不计。此外,视网膜变性的动物模型显示,视网膜小胶质细胞中的保护性群体中 CD68 的表达上调。在此,我们综述了 CD68 在调节视网膜色素上皮细胞健康和炎症方面的潜在作用 sub-retinal 空间,并讨论了在表现出 AMD 样特征的小鼠模型中其定位的观察结果。

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