Remodelling of smooth endoplasmic reticulum of Müller cells in aged human retina

IF 2.7 2区 医学 Q1 OPHTHALMOLOGY
Tapas C. Nag
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Abstract

The smooth endoplasmic reticulum (SER) is a system of interconnected cytoplasmic tubules with various subdomains, which can remodel in response to certain stimuli, as in the retinal pigment epithelium. Earlier studies reported Müller cells (MC) to contain the SER tubules as the main subdomain. A routine examination of postmortem human retinas (54–94 years; N = 8) revealed diverse SER subdomains in aged MC. Besides the presence of tubules with a distinct lumen, MC possessed tubules that were rather compressed, with partial to fully obliterated lumen. The other SER subdomains detected were lamellar and whorl that assembled near the endfeet plasma membrane. The compressed SER were quite longer, often curved and detected in MC endfeet and outer processes in Henle's fiber layer of aged macula (>80 years). No such features were detected in any cells of the peripheral retina nor in young donor retinas examined. Because lipid peroxidation was prominent in macular MC, it may be involved in the remodelling of SER shape. While the organized lamellar and whorl subdomains can be related to certain physiological demands, the peculiar SER subdomains with obliterated lumen could limit the normal functions of SER, e.g., calcium storage and carbohydrate metabolism.
老龄人视网膜上皮细胞光滑内质网的重构。
光滑内质网(SER)是一个相互连接的细胞质小管系统,具有不同的亚结构域,可以在某些刺激下重塑,如视网膜色素上皮。早期的研究报道了m ller细胞(MC)含有SER小管作为主要的子结构域。对人类死后视网膜(54-94岁,N=8)的常规检查显示,老年MC中存在多种SER亚结构域。除了存在具有明显管腔的小管外,MC还具有相当压缩的小管,管腔部分或完全消失。检测到的其他SER亚结构域是聚集在端足质膜附近的片层状和螺旋状。在老年黄斑(> ~ 80岁)中,压缩后的SER较长,常呈弯曲状,可见于MC端足和Henle纤维层外突。在周围视网膜细胞和年轻供体视网膜检查中均未发现此类特征。由于脂质过氧化在黄斑MC中表现突出,它可能参与了SER形状的重塑。虽然有组织的板层和轮状亚结构域可能与某些生理需求有关,但具有消失的管腔的特殊SER亚结构域可能限制SER的正常功能,例如钙储存和碳水化合物代谢。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Experimental eye research
Experimental eye research 医学-眼科学
CiteScore
6.80
自引率
5.90%
发文量
323
审稿时长
66 days
期刊介绍: The primary goal of Experimental Eye Research is to publish original research papers on all aspects of experimental biology of the eye and ocular tissues that seek to define the mechanisms of normal function and/or disease. Studies of ocular tissues that encompass the disciplines of cell biology, developmental biology, genetics, molecular biology, physiology, biochemistry, biophysics, immunology or microbiology are most welcomed. Manuscripts that are purely clinical or in a surgical area of ophthalmology are not appropriate for submission to Experimental Eye Research and if received will be returned without review.
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