Cui Y C, Tai P C, Gatter K C, Mason D Y, Spry C J
Immunology. 1983 May;49(1):183-9.
Human vascular endothelial cells were isolated by collagenase digestion of umbilical veins. Hybridomas secreting monoclonal antibodies were raised by fusing a mouse myeloma cell line to spleen cells from mice immunized with the isolated endothelial cells. A clone was selected which produced an antibody binding strongly to human umbilical vein endothelial cells. This antibody, EN 3, was shown to be directed against a major antigen on the surface of the cells, and appeared to be distinct from other antigens previously described on vascular tissues. The antibody bound to a lesser extent to umbilical artery endothelial cells and syncytiotrophoblast. Capillary endothelial cells in adult oesophageal tissues and tonsil were also labelled by the antibody, as were capillaries in a seminoma and infiltrating duct carcinoma of the breast. This well defined distribution in some foetal, adult and malignant tissues suggests that there is structural heterogeneity amongst endothelial cells in different sites, which may be linked to differences in differentiation or function.
通过胶原酶消化脐静脉来分离人血管内皮细胞。将小鼠骨髓瘤细胞系与用分离的内皮细胞免疫的小鼠脾细胞融合,产生分泌单克隆抗体的杂交瘤。选择了一个产生与人类脐静脉内皮细胞强烈结合的抗体的克隆。这种抗体EN 3被证明是针对细胞表面的一种主要抗原,并且似乎与先前在血管组织中描述的其他抗原不同。该抗体与脐动脉内皮细胞和合体滋养层细胞的结合程度较低。成人食管组织和扁桃体中的毛细血管内皮细胞以及精原细胞瘤和乳腺浸润性导管癌中的毛细血管也被该抗体标记。这种在一些胎儿、成人和恶性组织中明确的分布表明,不同部位的内皮细胞存在结构异质性,这可能与分化或功能的差异有关。