Ligation of cell surface heparan sulfate proteoglycans by antibody-coated beads stimulates phagocytic uptake into epithelial cells:: A model for cellular invasion by Neisseria gonorrhoeae

被引:44
作者
Dehio, C
Freissler, E
Lanz, C
Gómez-Duarte, OG
David, G
Meyer, TF
机构
[1] Max Planck Inst Biol, Infekt Biol Abt, D-72076 Tubingen, Germany
[2] Catholic Univ Louvain, Ctr Human Genet, B-3000 Louvain, Belgium
[3] Max Planck Inst Infekt Biol, Mol Biol Abt, D-10117 Berlin, Germany
关键词
heparan sulfate proteoglycan; phagocytosis; receptor; antibody; Neisseria gonorrhoeae; protein kinase C;
D O I
10.1006/excr.1998.4116
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Binding of a particular opacity outer membrane protein (Opa) of Neisseria,gonorrhoeae to cell surface heparan sulfate proteoglycans (HSPGs) of epithelial cells results in tight bacterial adherence; however, the role of this ligand-receptor interaction in triggering the subsequent bacterial internalization step is uncertain. Here we have used latex beads coated with HSPG-ligating antibodies as an in vitro model to study the role of HSPGs in gonococcal uptake into epithelial cells. Beads and gonococci showed the same cell line-specified adherence patterns and increase in phagocytic uptake mediated by serum or purified vitronectin (Vn). Heparitinase digestion as well as antibody competition experiments indicate that a critical level of HSPG ligation is necessary and sufficient to trigger phagocytic uptake into epithelial cells. Vn was found to specifically enhance HSPG-dependent phagocytic uptake while phagocytosis resulting from the ligation of other cell surface receptors was unaffected in the presence of Vn. Pharmacological studies with PKC inhibitors suggest a role for PHC in phagocytic uptake of HSPG-ligating beads. The use of drugs impairing cytoskeletal functions indicates that HSPG-dependent phagocytosis requires actin polymerization by a process distinct from receptor-mediated endocytosis, (C) 1998 Academic Press.
引用
收藏
页码:528 / 539
页数:12
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