SMOOTH-MUSCLE AND EPITHELIAL-CELLS EXPRESS SPECIFIC BINDING-SITES FOR THE C1Q COMPONENT OF COMPLEMENT

被引:17
作者
BORDIN, S
SMITH, M
GHEBREHIWET, B
ODA, D
PAGE, RC
机构
[1] UNIV WASHINGTON,DEPT PATHOL,SEATTLE,WA 98195
[2] UNIV WASHINGTON,DEPT ORAL BIOL,SEATTLE,WA 98195
[3] UNIV WASHINGTON,ORAL BIOL RES CTR,SEATTLE,WA 98195
[4] SUNY STONY BROOK,DEPT MED & PATHOL,STONY BROOK,NY 11794
来源
CLINICAL IMMUNOLOGY AND IMMUNOPATHOLOGY | 1992年 / 63卷 / 01期
关键词
D O I
10.1016/0090-1229(92)90093-4
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
In injury and inflammation, interactions of complement C1q with C1q receptors may provide attachment sites for cell localization and tissue regeneration. Cultured smooth muscle cells (58%), epithelial cells (26%), and endothelial cells (25%) attach to C1q-coated surfaces, while only 6% of cultured B cells (Raji) attach. Endothelial and Raji cells express C1q receptors, but C1q receptors (C1qR) on smooth muscle cells and epithelial cells have not previously been demonstrated. Evidence is provided that smooth muscle cells express an average of 1.5 × 106 C1qR/cell (Ka = 108 M-1) and that epithelial cells express and average of 0.7 × 106 C1qR/cell (Ka = 1.4 × 108 M-1). Binding properties of C1qR, and immunoreactivity to anti-C1qR antibodies, are characterized. The antibodiesspecifically recognize a 67-kDa component of smooth muscle cell lysates and inhibit cell attachment to C1q substrates. We conclude that distribution of C1qR may be ubiquitous; binding properties, size, and antigenicity of various C1qR may be related, but adhesive function may be tissue specific. © 1992.
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页码:51 / 57
页数:7
相关论文
共 45 条
[1]   CHARACTERIZATION OF THE CLQ RECEPTOR ON A HUMAN MACROPHAGE CELL-LINE, U937 [J].
ARVIEUX, J ;
REBOUL, A ;
BENSA, JC ;
COLOMB, MG .
BIOCHEMICAL JOURNAL, 1984, 218 (02) :547-555
[2]   HUMAN SMOOTH-MUSCLE VLA-1 INTEGRIN - PURIFICATION, SUBSTRATE-SPECIFICITY, LOCALIZATION IN AORTA, AND EXPRESSION DURING DEVELOPMENT [J].
BELKIN, VM ;
BELKIN, AM ;
KOTELIANSKY, VE .
JOURNAL OF CELL BIOLOGY, 1990, 111 (05) :2159-2170
[3]   BIOSYNTHESIS INVITRO OF COMPLEMENT SUBCOMPONENT-C1Q, SUBCOMPONENT-C1S AND SUBCOMPONENT-C1 INHIBITOR BY RESTING AND STIMULATED HUMAN-MONOCYTES [J].
BENSA, JC ;
REBOUL, A ;
COLOMB, MG .
BIOCHEMICAL JOURNAL, 1983, 216 (02) :385-392
[4]   PROTEIN-SYNTHESIS REQUIRES CELL-SURFACE CONTACT WHILE NUCLEAR EVENTS RESPOND TO CELL-SHAPE IN ANCHORAGE-DEPENDENT FIBROBLASTS [J].
BENZEEV, A ;
FARMER, SR ;
PENMAN, S .
CELL, 1980, 21 (02) :365-372
[5]  
BERMAN S, 1986, J IMMUNOL, V136, P1354
[6]   EFFECTS OF HUMAN SALIVA ON HEMOLYTIC ACTIVITY OF COMPLEMENT [J].
BOACKLE, RJ ;
PRUITT, KM ;
SILVERMAN, MS ;
GLYMPH, JL .
JOURNAL OF DENTAL RESEARCH, 1978, 57 (01) :103-110
[7]   DETECTION OF A HIGH-AFFINITY BINDING-SITE FOR THE GLOBULAR HEAD REGIONS OF THE C1Q COMPLEMENT PROTEIN ON A HUMAN-DIPLOID FIBROBLAST SUBTYPE [J].
BORDIN, S ;
PAGE, RC .
MOLECULAR IMMUNOLOGY, 1989, 26 (07) :677-685
[8]  
BORDIN S, 1983, J IMMUNOL, V130, P1871
[9]  
BORDIN S, 1990, J IMMUNOL, V145, P2520
[10]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3