Huang Wenbing, Chamberlain Coral G, Sarafian Richard Y, Chan-Ling Tailoi
School of Medical Sciences (Anatomy and Histology) and Bosch Institute, University of Sydney, Sydney, NSW 2006, Australia.
Neuron Glia Biol. 2008 Nov;4(4):285-94. doi: 10.1017/S1740925X0999007X. Epub 2009 Jul 6.
The aim of this study was to investigate the developmental expression of major histocompatibility complex class II (MHCII) by microglia and macrophages and their relationship to blood vessels in the retina, a representative tissue of the central nervous system. Such information is crucial to understanding the role of these cells in immune surveillance. Wholemount preparations of retinas from late embryonic, postnatal and adult rabbits were subjected to three-colour fluorescence microscopy using beta2 integrin (CD18) and MHCII antibodies and biotinylated Griffonia simplicifolia B4 isolectin labelling of blood vessels. CD18+ cells consistently exhibited characteristics of macrophages or microglia in the vascularized and non-vascularized regions of the retina, respectively. At all ages, MHCII was expressed by a high proportion of cells in the vascularized region, which contained macrophage-like 'parenchymal cells' as well as typical perivascular macrophages. MHCII expression by ramified microglia, first detected on postnatal day 30, was lower in the peripheral retina and intermediate in the avascular region of the myelinated streak. The observed localization of MHCII+ cells in relation to blood vessels and location-dependent differences in MHCII expression point to the possibility that these cells may be distributed strategically within the retina to provide multiple lines of defence against immune challenge arriving via the retinal vasculature.
本研究的目的是调查小胶质细胞和巨噬细胞主要组织相容性复合体II类(MHCII)的发育表达及其与视网膜(中枢神经系统的代表性组织)中血管的关系。此类信息对于理解这些细胞在免疫监视中的作用至关重要。使用β2整合素(CD18)和MHCII抗体以及生物素化的非洲相思树B4异凝集素对血管进行标记,对来自胚胎后期、出生后和成年兔子的视网膜整装标本进行三色荧光显微镜检查。CD18 +细胞分别在视网膜的血管化区域和非血管化区域始终表现出巨噬细胞或小胶质细胞的特征。在所有年龄段,MHCII在血管化区域的高比例细胞中表达,该区域包含巨噬细胞样“实质细胞”以及典型的血管周围巨噬细胞。分支状小胶质细胞的MHCII表达最早在出生后第30天检测到,在周边视网膜中较低,在有髓神经纤维束的无血管区域中处于中等水平。观察到的MHCII +细胞相对于血管的定位以及MHCII表达的位置依赖性差异表明,这些细胞可能在视网膜内进行策略性分布,以提供针对通过视网膜血管系统到来的免疫挑战的多道防线。