Misek D E, Bard E, Rodriguez-Boulan E
Cell. 1984 Dec;39(3 Pt 2):537-46. doi: 10.1016/0092-8674(84)90460-4.
To study the biogenetic pathway of influenza hemagglutinin (HA), a model apical glycoprotein, in polarized epithelial MDCK cells, anti-HA antibodies were added to the basolateral surface during influenza infection. In monolayers grown on collagen gels influenza and VSV plaque development was blocked only when the antibodies were added to the respective budding surface. Addition of anti-HA antibodies to the basal medium of monolayers grown on nitrocellulose filter chambers neither resulted in HA-coupled transport of antibody nor inhibited HA migration to the apical surface. These results indicate that the bulk of HA is vectorially inserted into the apical surface of MDCK cells by polarized exocytosis. Other apical proteins in epithelia may use a similar mechanism during biogenesis.
为了研究流感血凝素(HA)——一种典型的顶端糖蛋白——在极化上皮MDCK细胞中的生物发生途径,在流感感染期间将抗HA抗体添加到基底外侧表面。在胶原凝胶上生长的单层细胞中,只有当抗体添加到各自的出芽表面时,流感病毒和水泡性口炎病毒(VSV)斑块的形成才会被阻断。将抗HA抗体添加到在硝酸纤维素滤膜小室上生长的单层细胞的基础培养基中,既不会导致抗体与HA偶联转运,也不会抑制HA向顶端表面的迁移。这些结果表明,大部分HA通过极化胞吐作用定向插入MDCK细胞的顶端表面。上皮细胞中的其他顶端蛋白在生物发生过程中可能使用类似的机制。