SOLUBLE CD14 PARTICIPATES IN THE RESPONSE OF CELLS TO LIPOPOLYSACCHARIDE

被引:647
作者
FREY, EA
MILLER, DS
JAHR, TG
SUNDAN, A
BAZIL, V
ESPEVIK, T
FINLAY, BB
WRIGHT, SD
机构
[1] ROCKEFELLER UNIV, CELLULAR PHYSIOL & IMMUNOL LAB, 1230 YORK AVE, NEW YORK, NY 10021 USA
[2] UNIV BRITISH COLUMBIA, DEPT BIOCHEM, BIOTECHNOL LAB, VANCOUVER V6T 1Z3, BC, CANADA
[3] UNIV BRITISH COLUMBIA, DEPT MICROBIOL, VANCOUVER V6T 1Z3, BC, CANADA
[4] INST CANC RES, N-7005 TRONDHEIM, NORWAY
[5] CZECHOSLOVAK ACAD SCI, INST MOLEC GENET, CS-14220 PRAGUE 4, CZECHOSLOVAKIA
关键词
D O I
10.1084/jem.176.6.1665
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
CD14 is a 55-kD protein found both as a glycosylphosphatidyl inositol-linked protein on the surface of mononuclear phagocytes and as a soluble protein in the blood. CD14 on the cell membrane (mCD14) has been shown to serve as a receptor for complexes of lipopolysaccharide (LPS) with LPS binding protein, but a function for soluble CD14 (sCD14) has not been described. Here we show that sCD14 enables responses to LPS by cells that do not express CD14. We have examined induction of endothelial-leukocyte adhesion molecule 1 expression by human umbilical vein endothelial cells, interleukin 6 secretion by U373 astrocytoma cells, and cytotoxicity of bovine endothelial cells. None of these cell types express mCD14, yet all respond to LPS in a serum-dependent fashion, and all responses are completely blocked by anti-CD14 antibodies. Immunodepletion of sCD14 from serum prevents responses to LPS, and the responses are restored by addition of sCD14. These studies suggest that a surface anchor is not needed for the function of CD14 and further imply that sCD14 must bind to additional proteins on the cell surface to associate with the cell and transduce a signal. They also indicate that sCD14 may have an important role in potentiating responses to LPS in cells lacking mCD14.
引用
收藏
页码:1665 / 1671
页数:7
相关论文
共 25 条
[1]   PRODUCTION OF HYBRIDOMA GROWTH-FACTOR BY HUMAN-MONOCYTES [J].
AARDEN, LA ;
DEGROOT, ER ;
SCHAAP, OL ;
LANSDORP, PM .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1987, 17 (10) :1411-1416
[2]   BIOCHEMICAL-CHARACTERIZATION OF A SOLUBLE FORM OF THE 53-KDA MONOCYTE SURFACE-ANTIGEN [J].
BAZIL, V ;
HOREJSI, V ;
BAUDYS, M ;
KRISTOFOVA, H ;
STROMINGER, JL ;
KOSTKA, W ;
HILGERT, I .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1986, 16 (12) :1583-1589
[3]  
BAZIL V, 1991, J IMMUNOL, V147, P1567
[4]  
BEEKHUIZEN H, 1991, J IMMUNOL, V147, P3761
[5]   A BLOCKING MONOCLONAL-ANTIBODY TO ENDOTHELIAL-LEUKOCYTE ADHESION MOLECULE-1 (ELAM1) [J].
BENJAMIN, C ;
DOUGAS, I ;
CHIROSSO, G ;
LUHOWSKYJ, S ;
ROSA, M ;
NEWMAN, B ;
OSBORN, L ;
VASSALLO, C ;
HESSION, C ;
GOELZ, S ;
MCCARTHY, K ;
LOBB, R .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1990, 171 (01) :348-353
[6]   IDENTIFICATION OF AN INDUCIBLE ENDOTHELIAL LEUKOCYTE ADHESION MOLECULE [J].
BEVILACQUA, MP ;
POBER, JS ;
MENDRICK, DL ;
COTRAN, RS ;
GIMBRONE, MA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1987, 84 (24) :9238-9242
[7]   PROCEDURE FOR ISOLATION OF BACTERIAL LIPOPOLYSACCHARIDES FROM BOTH SMOOTH AND ROUGH PSEUDOMONAS-AERUGINOSA AND SALMONELLA-TYPHIMURIUM STRAINS [J].
DARVEAU, RP ;
HANCOCK, REW .
JOURNAL OF BACTERIOLOGY, 1983, 155 (02) :831-838
[8]  
ESPEVIK T, 1992, IN PRESS EUR J IMMUN
[9]  
HAZIOT A, 1988, J IMMUNOL, V141, P547
[10]  
JIRIK FR, 1989, J IMMUNOL, V142, P144