Suppr超能文献

人类视网膜中小胶质细胞形态的发育

Development of microglial topography in human retina.

作者信息

Diaz-Araya C M, Provis J M, Penfold P L, Billson F A

机构信息

Save Sight and Eye Health Institute, Department of Clinical Ophthalmology, University of Sydney, N.S.W., Australia.

出版信息

J Comp Neurol. 1995 Dec 4;363(1):53-68. doi: 10.1002/cne.903630106.

Abstract

The development of microglial topography in wholemounts of human retina has been examined in the age range 10-25 weeks gestation (WG) using histochemistry and immunohistochemistry for CD45 and major histocompatibility complex class II antigens. Microglia were present in three planes corresponding to the developing nerve fibre layer/ganglion cell layer, the inner plexiform layer and the outer plexiform layer. Distribution patterns of cells through the retinal thickness and across the retinal surface area varied with gestational age. Microglia were elongated in superficial retina, large and ramified in the middle plane, and small, rounded and less ramified in deep retina. Intensely labeled, rounded profiles seen at the pars caeca of the ciliary processes, the retinal margin and at the optic disc may represent precursors of some retinal microglia. At 10 WG, the highest densities of microglia were present in middle and deep retina in the far periphery and at the retinal margin, with few superficial microglia evident centrally at the optic disc. At 14 WG, high densities of microglia were apparent superficially at the optic disc; microglia of middle and deep retina were distributed at more central locations although continuing to concentrate in the retinal periphery. Microglia appear to migrate into the developing human retina from two mains sources, the retinal margin and the optic disc, most likely originating from the blood vessels of the ciliary body and iris, and the retinal vasculature, respectively. The data suggest that the development of microglial topography occurs in two phases, an early phase occurring prior to vascularization, and a late phase associated with the development of the retinal vasculature.

摘要

利用针对CD45和主要组织相容性复合体II类抗原的组织化学和免疫组织化学方法,对妊娠10 - 25周(WG)的人视网膜整装片中的小胶质细胞形态发展进行了研究。小胶质细胞存在于三个平面,分别对应于发育中的神经纤维层/神经节细胞层、内网状层和外网状层。整个视网膜厚度和视网膜表面积上细胞的分布模式随胎龄而变化。小胶质细胞在视网膜浅层呈细长形,在中间平面大且有分支,在视网膜深层小、呈圆形且分支较少。在睫状突盲部、视网膜边缘和视盘处可见的强染色圆形轮廓可能代表一些视网膜小胶质细胞的前体。在妊娠10周时,小胶质细胞密度最高的区域位于远周边和视网膜边缘的视网膜中层和深层,视盘中央的浅层小胶质细胞较少。在妊娠14周时,视盘表面可见高密度的小胶质细胞;视网膜中层和深层的小胶质细胞分布在更中央的位置,尽管仍集中在视网膜周边。小胶质细胞似乎从两个主要来源迁移到发育中的人视网膜,即视网膜边缘和视盘,最有可能分别起源于睫状体和虹膜的血管以及视网膜血管系统。数据表明,小胶质细胞形态的发展分两个阶段进行,早期阶段发生在血管化之前,晚期阶段与视网膜血管系统的发育相关。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验