Wolosin J M, Schütte M, Chen S
Department of Ophthalmology, Mount Sinai School of Medicine, New York, New York 10029, USA.
Invest Ophthalmol Vis Sci. 1997 Feb;38(2):341-8.
To evaluate the distribution of different alpha- and beta-type connexins (Cx) present in the dual layered ciliary body epithelia (CBE) of both rabbit and rat.
Immunocytochemical detection of Cx26, Cx32, Cx43, and Cx50 was performed on frozen sections of rabbit and rat ciliary body using indirect immunofluorescent methods. The identity of the antigens recognized by the monoclonal primary antibodies was further confirmed by Western immunoblots. Double labeling experiments based on either conventional or confocal microscopy were carried out to establish the exact spatial relationship between different connexins.
Connexin 50 was found only in the nonpigmented epithelium (NPE) at apical and basolateral membranes, whereas Cx43 was observed exclusively and at a very high concentration in the pigmented epithelium (PE), primarily in the apical cell membrane, with minimal extension to the proximal lateral zone. The correct antigenicity of the antibodies was confirmed by Western blots of rabbit ciliary body membranes. In rabbit, the Cx26 antibody detected an antigen that was abundant in the NPE and was weakly expressed in the PE. In rat, however, the Cx26 staining was confined to capillary wall endothelia. Western blots of ciliary body and liver membranes and liver immunohistology indicated that the Cx26 antibody used does not recognize rabbit Cx26. Cx32 did not yield any substantial epithelial labeling in either species.
The distribution of Cx50 around the entire NPE cell perimeter suggests its involvement in NPE-NPE cell homotypic gap junctions. The concentration of Cx43 and Cx50 at the apical membranes of the PE and NPE cells, respectively, and their complete absence from the opposite cell suggest that these connexins may participate in the formation of heterotypic gap junctions, either with each other or with other yet unidentified connexins.
评估兔和大鼠双层睫状体上皮(CBE)中存在的不同α型和β型连接蛋白(Cx)的分布情况。
采用间接免疫荧光法,对兔和大鼠睫状体的冰冻切片进行Cx26、Cx32、Cx43和Cx50的免疫细胞化学检测。通过Western免疫印迹进一步确认单克隆一抗识别的抗原的同一性。基于传统显微镜或共聚焦显微镜进行双重标记实验,以确定不同连接蛋白之间的确切空间关系。
连接蛋白50仅在无色素上皮(NPE)的顶端和基底外侧膜中发现,而Cx43仅在色素上皮(PE)中以非常高的浓度观察到,主要在顶端细胞膜中,向近端外侧区域的延伸极少。兔睫状体膜的Western印迹证实了抗体的正确抗原性。在兔中,Cx26抗体检测到一种在NPE中丰富且在PE中弱表达的抗原。然而,在大鼠中,Cx26染色局限于毛细血管壁内皮细胞。睫状体和肝膜的Western印迹以及肝脏免疫组织学表明,所使用的Cx26抗体不能识别兔Cx26。Cx32在这两个物种中均未产生任何实质性的上皮标记。
Cx50在整个NPE细胞周边的分布表明其参与NPE - NPE细胞同型间隙连接。Cx43和Cx50分别在PE和NPE细胞的顶端膜中的浓度以及在相对细胞中完全不存在,表明这些连接蛋白可能相互之间或与其他尚未鉴定的连接蛋白参与异型间隙连接的形成。