Okami T, Yamamoto A, Omori K, Takada T, Uyama M, Tashiro Y
Department of Physiology, Kansai Medical University, Osaka, Japan.
J Histochem Cytochem. 1990 Sep;38(9):1267-75. doi: 10.1177/38.9.2167328.
We investigated quantitatively the ultrastructural localization of the alpha-subunit of Na+,K(+)-ATPase in rat retinal pigment epithelial cells by the protein A-gold technique, using an affinity-purified antibody against the alpha-subunit of rat kidney Na+,K(+)-ATPase. Immunoblot analysis showed that the antibody bound specifically to the alpha- and alpha(+)-subunits of Na+,K(+)-ATPase in the whole retina [the sensory retina plus retinal pigment epithelium (RPE)]. Rat eyes were fixed by perfusion with 4% paraformaldehyde containing 1% glutaraldehyde and embedded in Lowicryl K4M. Ultra-thin sections were incubated with affinity-purified antibody against the alpha-subunit of rat kidney Na+,K(+)-ATPase and subsequently with protein A-gold complex. Light microscopy with a silver enhancement procedure revealed Na+,K(+)-ATPase localized to both the apical and the basal plasma membrane domains of the RPE. Quantitative immunocytochemical analysis by electron microscopy showed a higher density of gold particles on the apical surface than on the basolateral one. Microvilli are so well developed on the apical surface of the RPE that the apical surface profile is much longer than the basolateral one. This means that Na+,K(+)-ATPase is mainly located on the apical surface of the RPE cells.
我们使用针对大鼠肾Na⁺,K⁺-ATP酶α亚基的亲和纯化抗体,通过蛋白A-金技术对大鼠视网膜色素上皮细胞中Na⁺,K⁺-ATP酶α亚基进行了超微结构定位的定量研究。免疫印迹分析表明,该抗体与整个视网膜[感觉视网膜加视网膜色素上皮(RPE)]中的Na⁺,K⁺-ATP酶α亚基和α⁺亚基特异性结合。大鼠眼睛通过灌注含1%戊二醛的4%多聚甲醛固定,并包埋在Lowicryl K4M中。超薄切片与针对大鼠肾Na⁺,K⁺-ATP酶α亚基的亲和纯化抗体孵育,随后与蛋白A-金复合物孵育。采用银增强程序的光学显微镜显示,Na⁺,K⁺-ATP酶定位于RPE的顶端和基底质膜结构域。电子显微镜定量免疫细胞化学分析显示,顶端表面的金颗粒密度高于基底外侧表面。RPE顶端表面的微绒毛非常发达,以至于顶端表面轮廓比基底外侧表面长得多。这意味着Na⁺,K⁺-ATP酶主要位于RPE细胞的顶端表面。