The soil and the seed: The relationship between Descemet's membrane and the corneal endothelium

被引:4
|
作者
Petrela, Redion B. [1 ,2 ]
Patel, Sangita P. [1 ,3 ]
机构
[1] SUNY Buffalo, Ross Eye Inst, Jacobs Sch Med & Biomed Sci, Dept Ophthalmol, 1176 Main St, Buffalo, NY 14209 USA
[2] State Univ New York Upstate Med Univ, Norton Coll Med, 750 East Adams St, Syracuse, NY 13210 USA
[3] Vet Adm Western New York Healthcare Syst, Res & Ophthalmol Serv, 3495 Bailey Ave, Buffalo, NY 14215 USA
基金
美国国家卫生研究院;
关键词
Fuchs endothelial dystrophy; Corneal endothelium; Descemet?s membrane; Guttae; Extracellular matrix; TRIPLET REPEAT EXPANSION; EXTRACELLULAR-MATRIX; MARFAN-SYNDROME; RNA FOCI; MYOTONIC-DYSTROPHY; OXIDATIVE STRESS; FUCHS DYSTROPHY; COLLAGEN; CELLS; PROLIFERATION;
D O I
10.1016/j.exer.2022.109376
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Descemet's membrane (DM), the basement membrane of the corneal endothelium, is formed from the extra -cellular matrix (ECM) secreted by corneal endothelial cells. The ECM supports the growth and function of the corneal endothelial cells. Changes to DM are central to the diagnosis of the most common corneal endothelial disease, Fuchs endothelial corneal dystrophy (FECD). Changes in DM are also noted in systemic diseases such as diabetes mellitus. In FECD, the DM progressively accumulates guttae, "drop-like deposits" that disrupt the corneal endothelial cell monolayer. While the pathophysiologic changes to corneal endothelial cells in the course of FECD have been well described and reviewed, the changes to DM have received limited attention. The reci-procity of influence between the corneal endothelial cells and DM demands full attention to the latter in our search for novel treatment and preventive strategies. In this review, we discuss what is known about the for-mation and composition of DM and how it changes in FECD and other conditions. We review characteristics of guttae and the interplay between corneal endothelial cells and guttae, particularly as it might apply to future cell -based and genetic therapies for FECD.
引用
收藏
页数:9
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