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人视神经乳头星形胶质细胞和筛板细胞的分离和鉴定。

Isolation and characterization of human optic nerve head astrocytes and lamina cribrosa cells.

机构信息

The North Texas Eye Research Institute, Department of Pharmacology and Neuroscience, University of North Texas Health Science Center at Fort Worth, Fort Worth, 3500 Camp Bowie Blvd., Fort Worth, TX, 76107, United States.

The North Texas Eye Research Institute, Department of Pharmacology and Neuroscience, University of North Texas Health Science Center at Fort Worth, Fort Worth, 3500 Camp Bowie Blvd., Fort Worth, TX, 76107, United States.

出版信息

Exp Eye Res. 2020 Aug;197:108103. doi: 10.1016/j.exer.2020.108103. Epub 2020 Jun 6.

Abstract

The lamina cribrosa is the initial site of glaucomatous injury. Pathological changes to the lamina cribrosa include posterior displacement of the lamina cribrosa, loss of trophic support, and remodeling of the extracellular matrix. Optic nerve head (ONH) astrocytes and lamina cribrosa cells synthesize extracellular matrix proteins to support and maintain the lamina cribrosa under physiological conditions. During glaucoma, these cells respond to mechanical strain and other stimuli, which leads to pathological remodeling of the ONH. Although ONH astrocytes and lamina cribrosa cells have been previously cultured, there is no well-accepted, straightforward technique to isolate both cell types from a single dissected human ONH. To better understand the pathophysiology of glaucoma, we obtained and cultured lamina cribrosa explants from human donor eyes. Initially, cells that grew out from the explant were ONH astrocytes and lamina cribrosa cells. Using a specialized medium, we isolated pure populations of lamina cribrosa cells and ONH astrocytes. ONH astrocytes expressed glial fibrillary acidic protein (GFAP). Lamina cribrosa cells expressed alpha-smooth muscle actin (α-SMA), but were negative for GFAP. This method of ONH cell isolation and cell-culture will provide a technique to better understand the molecular and cell-specific changes in glaucomatous damage to the ONH.

摘要

筛板是青光眼损伤的初始部位。筛板的病理性变化包括筛板后移位、营养支持丧失和细胞外基质重塑。视神经头部(ONH)星形胶质细胞和筛板细胞合成细胞外基质蛋白,在生理条件下支持和维持筛板。在青光眼期间,这些细胞对机械应变和其他刺激作出反应,导致 ONH 的病理性重塑。尽管已经对 ONH 星形胶质细胞和筛板细胞进行了先前的培养,但没有一种被广泛接受的简单技术可以从单个解剖的人 ONH 中分离这两种细胞类型。为了更好地理解青光眼的病理生理学,我们从人供体眼中获得并培养了筛板外植体。最初,从外植体中生长出来的细胞是 ONH 星形胶质细胞和筛板细胞。使用专门的培养基,我们分离出了纯的筛板细胞和 ONH 星形胶质细胞群体。ONH 星形胶质细胞表达神经胶质纤维酸性蛋白(GFAP)。筛板细胞表达α-平滑肌肌动蛋白(α-SMA),但不表达 GFAP。这种 ONH 细胞分离和细胞培养方法将提供一种技术,以更好地理解青光眼对 ONH 的损害的分子和细胞特异性变化。

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