Hirt R P, Hughes G J, Frutiger S, Michetti P, Perregaux C, Poulain-Godefroy O, Jeanguenat N, Neutra M R, Kraehenbuhl J P
Swiss Institute for Experimental Cancer Research, University of Lausanne, Epalinges.
Cell. 1993 Jul 30;74(2):245-55. doi: 10.1016/0092-8674(93)90416-n.
MDCK cells expressing the polymeric immunoglobulin (poly-Ig) receptor, cocultured with IgA-producing hybridoma cells, transported dimeric IgA (dIgA) from the basolateral into the lumenal compartment, where it was recovered as secretory component-dIgA complexes. The tail of the receptor was phosphorylated on serines 664 and 726. Each serine was mutated to alanine. Appearance of A726 receptor at the basolateral surface was reduced approximately 5-fold. This was accompanied by a approximately 5-fold reduction in dIgA transcytosis. Basolateral delivery of receptor was not affected by mutation A664, and in the absence of dIgA, the receptor accumulated in recycling basolateral endosomes. In coculture, however, dIgA transcytosis by A664 receptor was normal. Thus, entry of receptor into the transcytotic pathway requires Ser-664 phosphorylation only in the absence of dIgA.
表达聚合免疫球蛋白(poly-Ig)受体的MDCK细胞与产生IgA的杂交瘤细胞共培养时,可将二聚体IgA(dIgA)从基底外侧转运至管腔隔室,在那里它以分泌成分-dIgA复合物的形式被回收。受体的尾部在丝氨酸664和726处发生磷酸化。每个丝氨酸都被突变为丙氨酸。A726受体在基底外侧表面的出现减少了约5倍。这伴随着dIgA转胞吞作用减少约5倍。受体的基底外侧递送不受A664突变的影响,并且在没有dIgA的情况下,受体在循环的基底外侧内体中积累。然而,在共培养中,A664受体的dIgA转胞吞作用是正常的。因此,仅在没有dIgA的情况下,受体进入转胞吞途径才需要Ser-664磷酸化。