Langer M G, Sundarraj C V, Sundarraj N
J Embryol Exp Morphol. 1986 Jun;94:163-72.
Monoclonal antibodies, specific against cell surface differentiation antigens of human corneal epithelial cells, were developed using epithelial cells resected from human corneas as the immunogens. One of these antibodies reacted specifically with corneal epithelial cells and not with epithelial cells of other tissues when tested by an indirect immunoperoxidase technique. Nonidet P-40 extracts of different subcellular fractions of human corneal epithelial cells were tested for their reactivity against this antibody using an enzyme-linked immunosorbent assay. The results indicated that the antigen recognized by this antibody is associated with the plasma membrane. This was further verified by immuno-electron-microscopic analysis using ferritin-conjugated anti-mouse IgG antibody. This antigen was not detectable in the corneal epithelial cells in primary cultures nor in the epithelial cells from early stages of developing cornea (12 to 18 weeks in utero) but was present in the epithelial cells in the corneas of an 8-month-old infant. Therefore, this surface-associated antigen identified in the present study is a developmentally regulated marker of human corneal epithelium.
以从人角膜切除的上皮细胞作为免疫原,制备了针对人角膜上皮细胞表面分化抗原的单克隆抗体。当通过间接免疫过氧化物酶技术检测时,其中一种抗体与角膜上皮细胞特异性反应,而不与其他组织的上皮细胞反应。使用酶联免疫吸附测定法,检测了人角膜上皮细胞不同亚细胞组分的Nonidet P - 40提取物与该抗体的反应性。结果表明,该抗体识别的抗原与质膜相关。使用铁蛋白偶联的抗小鼠IgG抗体进行免疫电子显微镜分析进一步证实了这一点。在原代培养的角膜上皮细胞中以及发育中角膜早期阶段(子宫内12至18周)的上皮细胞中均未检测到该抗原,但在一名8个月大婴儿的角膜上皮细胞中存在。因此,本研究中鉴定的这种表面相关抗原是人类角膜上皮的一种发育调控标志物。