BIDIRECTIONAL TRANSCYTOSIS DETERMINES THE STEADY-STATE DISTRIBUTION OF THE TRANSFERRIN RECEPTOR AT OPPOSITE PLASMA-MEMBRANE DOMAINS OF BEWO CELLS

被引:31
作者
CERNEUS, DP [1 ]
STROUS, GJ [1 ]
VANDERENDE, A [1 ]
机构
[1] UNIV UTRECHT,SCH MED,DEPT CELL BIOL,AZU H02 314,HEIDELBERGLAAN 100,3584 CH UTRECHT,NETHERLANDS
关键词
D O I
10.1083/jcb.122.6.1223
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Trophoblast-like BeWo cells form well-polarized epithelial monolayers, when cultured on permeable supports. Contrary to other polarized cell systems, in which the transferrin receptor is found predominantly on the basolateral cell surface, BeWo cells express the transferrin receptor at both apical and basolateral cell surfaces (Cerneus, D.P., and A. van der Ende. 1991. J. Cell Biol. 114: 1149-1158). In the present study we have addressed the question whether BeWo cells use a different sorting mechanism to target transferrin receptors to the cell surface, by examining the biosynthetic and transcytotic pathways of the transferrin receptor in BeWo cells. Using trypsin and antibodies to detect transferrin receptors at the cell surface of filter-grown BeWo cells, we show that at least 80% of newly synthesized transferrin receptor follows a direct pathway to the basolateral surface, demonstrating that the transferrin receptor is efficiently intracellularly sorted. After surface arrival, pulse-labeled transferrin receptor equilibrates between apical and basolateral cell surfaces, due to ongoing transcytotic transport in both directions. The subsequent redistribution takes over 120 min and results in a steady state distribution with 1.5-2.0 times more transferrin receptors at the basolateral surface than at the apical surface. By monitoring the fate of surface-bound I-125-transferrin, internalized either from the apical or basolateral surface transcytosis of the transferrin receptor was studied. About 15% of I-125-transferrin is transcytosed in the basolateral to apical direction, whereas 25% is transcytosed in the opposite direction, indicated that the fraction of receptors involved in transcytosis is roughly twofold higher for the apical receptor pool, as compared to the basolateral pool. Upon internalization, both apical and basolateral receptor pools become redistributed on both surfaces, resulting in a twofold higher number of transferrin receptors at the basolateral surface. Our results indicate that in BeWo cells bidirectional transcytosis is the main factor in surface distribution of transferrin receptors on apical and basolateral surfaces, which may represent a cell type-specific, post-endocytic, sorting mechanism.
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页码:1223 / 1230
页数:8
相关论文
共 24 条
[1]   BIOGENESIS OF THE RAT HEPATOCYTE PLASMA-MEMBRANE INVIVO - COMPARISON OF THE PATHWAYS TAKEN BY APICAL AND BASOLATERAL PROTEINS USING SUBCELLULAR FRACTIONATION [J].
BARTLES, JR ;
FERACCI, HM ;
STIEGER, B ;
HUBBARD, AL .
JOURNAL OF CELL BIOLOGY, 1987, 105 (03) :1241-1251
[2]   POSTENDOCYTOTIC SORTING OF THE LIGAND FOR THE POLYMERIC IMMUNOGLOBULIN RECEPTOR IN MADIN-DARBY CANINE KIDNEY-CELLS [J].
BREITFELD, PP ;
HARRIS, JM ;
MOSTOV, KE .
JOURNAL OF CELL BIOLOGY, 1989, 109 (02) :475-486
[3]   A SINGLE AMINO-ACID CHANGE IN THE CYTOPLASMIC DOMAIN ALTERS THE POLARIZED DELIVERY OF INFLUENZA-VIRUS HEMAGGLUTININ [J].
BREWER, CB ;
ROTH, MG .
JOURNAL OF CELL BIOLOGY, 1991, 114 (03) :413-421
[4]   AN AUTONOMOUS SIGNAL FOR BASOLATERAL SORTING IN THE CYTOPLASMIC DOMAIN OF THE POLYMERIC IMMUNOGLOBULIN RECEPTOR [J].
CASANOVA, JE ;
APODACA, G ;
MOSTOV, KE .
CELL, 1991, 66 (01) :65-75
[5]   APICAL AND BASOLATERAL TRANSFERRIN RECEPTORS IN POLARIZED BEWO CELLS RECYCLE THROUGH SEPARATE ENDOSOMES [J].
CERNEUS, DP ;
VANDERENDE, A .
JOURNAL OF CELL BIOLOGY, 1991, 114 (06) :1149-1158
[6]  
CERNEUS DP, 1993, J BIOL CHEM, V268, P3150
[7]   TRANSPLANTED LDL AND MANNOSE-6-PHOSPHATE RECEPTOR INTERNALIZATION SIGNALS PROMOTE HIGH-EFFICIENCY ENDOCYTOSIS OF THE TRANSFERRIN RECEPTOR [J].
COLLAWN, JF ;
KUHN, LA ;
LIU, LFS ;
TAINER, JA ;
TROWBRIDGE, IS .
EMBO JOURNAL, 1991, 10 (11) :3247-3253
[8]   TRANSFERRIN RECEPTOR INTERNALIZATION SEQUENCE YXRF IMPLICATES A TIGHT TURN AS THE STRUCTURAL RECOGNITION MOTIF FOR ENDOCYTOSIS [J].
COLLAWN, JF ;
STANGEL, M ;
KUHN, LA ;
ESEKOGWU, V ;
JING, SQ ;
TROWBRIDGE, IS ;
TAINER, JA .
CELL, 1990, 63 (05) :1061-1072
[9]   THE INTERNALIZATION SIGNAL AND THE PHOSPHORYLATION SITE OF TRANSFERRIN RECEPTOR ARE DISTINCT FROM THE MAIN BASOLATERAL SORTING INFORMATION [J].
DARGEMONT, C ;
LEBIVIC, A ;
ROTHENBERGER, S ;
IACOPETTA, B ;
KUHN, LC .
EMBO JOURNAL, 1993, 12 (04) :1713-1721
[10]   TRANSFERRIN RECEPTOR POLARITY AND RECYCLING ACCURACY IN TIGHT AND LEAKY STRAINS OF MADIN-DARBY CANINE KIDNEY-CELLS [J].
FULLER, SD ;
SIMONS, K .
JOURNAL OF CELL BIOLOGY, 1986, 103 (05) :1767-1779