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人视网膜中玻璃体胶原蛋白(II型)的包裹:出生后胶原蛋白更新的一个指标?

Packages of vitreous collagen (type II) in the human retina: an indication of postnatal collagen turnover?

作者信息

Ponsioen Theodorus L, van der Worp Roelofje J, van Luyn Marja J A, Hooymans Johanna M M, Los Leonoor I

机构信息

Department of Ophthalmology, University Hospital/University of Groningen, P.O. Box 30.001, 9700 RB Groningen, The Netherlands.

出版信息

Exp Eye Res. 2005 May;80(5):643-50. doi: 10.1016/j.exer.2004.11.014. Epub 2005 Jan 4.

Abstract

The purpose of this study was to evaluate the vitreoretinal border in the (pre-)equatorial area in nonpathologic human donor eyes, because the majority of retinal defects induced by posterior vitreous detachment (PVD) are located there. Nine eyes (24-80 years) were fixed and embedded in Technovit 8100. After evaluation by light microscope, areas of interest were selected for immunotransmission electron microscope. Anti-type II collagen antibody was used to stain vitreous fibrils and lamellae; anti-type IV collagen antibody was used to identify the internal limiting lamina (ILL); anti-vimentin and anti-CD-68 antibodies stained retinal Muller cells and macrophages, respectively. Observations included fusing of lamellae with the ILL, an intravitreal course of the ILL, and clear focal interruptions in the ILL. In addition, an obvious finding was the presence of intraretinal packages of type II collagen. Interestingly these collagen packages were closely related to Muller cells and, in several eyes, also to macrophages, cell debris and interruptions in the ILL. In our opinion, the collagen packages can reflect the net result of a process of interactive remodelling, in which both breakdown and synthesis of vitreous and ILL collagens take place. Connections between vitreous and intraretinal collagen networks can make the (pre-)equatorial area more vulnerable to tearing and retinal detachment in the case of liquefaction and PVD.

摘要

本研究的目的是评估非病理性人类供体眼赤道前区域的玻璃体视网膜边界,因为大多数由玻璃体后脱离(PVD)引起的视网膜缺损都位于该区域。9只年龄在24至80岁之间的眼睛被固定并包埋于Technovit 8100中。经光学显微镜评估后,选择感兴趣的区域进行免疫透射电子显微镜检查。使用抗II型胶原抗体对玻璃体纤维和板层进行染色;使用抗IV型胶原抗体识别内界膜(ILL);抗波形蛋白和抗CD-68抗体分别对视网膜Müller细胞和巨噬细胞进行染色。观察结果包括板层与ILL的融合、ILL的玻璃体内走行以及ILL中明显的局灶性中断。此外,一个明显的发现是视网膜内存在II型胶原包块。有趣的是,这些胶原包块与Müller细胞密切相关,在几只眼中还与巨噬细胞、细胞碎片以及ILL的中断有关。我们认为,胶原包块可以反映一个交互重塑过程的最终结果,在这个过程中,玻璃体和ILL胶原的分解和合成都会发生。在液化和PVD的情况下,玻璃体与视网膜内胶原网络之间的连接会使赤道前区域更容易发生撕裂和视网膜脱离。

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