ORGAN-SPECIFIC AND NON-ORGAN-SPECIFIC LYMPHOCYTE RECEPTORS FOR VASCULAR ENDOTHELIUM

被引:18
作者
CAVENDER, DE
机构
[1] Department of Microbiology and Immunology, University of Miami School of Medicine, Miami, FL
关键词
D O I
10.1111/1523-1747.ep12875042
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
The recirculation of lymphocytes from blood to lymph and back to blood is necessary for the proper functioning of the immune system as it facilitates interactions between antigen-reactive clones of lymphocytes and antigen-presenting cells. The first step in the emigration of a blood-borne lymphocyte into either a secondary lymphoid organ or an inflammatory lesion is its adherence to vascular endothelial cells (EC) lining unique post-capillary venules known as high endothelial venules (HEV). Several groups have recently cloned and sequenced genes which may encode organ-specific lymphocyte receptors for the EC of such HEV. The extracellular portion of the putative murine lymphocyte homing receptor for peripheral lymph node HEV is composed of an N-terminal lectin-like domain, followed by an epidermal growth factor-like domain, and then two identical repeating domains which are homologous to a number of complement-binding proteins. A hydrophobic transmembrane domain and a cytoplasmic tail complete the structure. A very similar gene structure has been reported for a cytokine-inducible EC surface protein which is involved in neutrophil-EC adhesion in vitro. In marked contrast, the gene for a putative human lymphocyte homing receptor appears to belong to a gene family which encodes cell-surface molecules with receptor activity for extracellular matrix (ECM) proteins. Similarly, the cell-surface molecule which appears to be the murine lymphocyte receptor for Peyer's patch HEV is homologous, if not identical, to the human VLA-4 molecule, another receptor with binding activity for an ECM protein. It has also been demonstrated that lymphocyte function-associated antigen 1 (LFA-1) acts in a non-organ-specific manner to mediate lymphocyte-EC adhesion. Finally, other non-organ-specific lymphocyte adhesion molecules for EC may include CD4 and CD8 (which bind to class II and class I MHC antigens, respectively), and CD2 (which binds to LFA-3). © 1990.
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页码:S41 / S48
页数:8
相关论文
共 78 条
[41]  
KANSAS GS, 1989, J IMMUNOL, V142, P3050
[42]   TOWARDS A BETTER DEFINITION OF HUMAN-LEUKOCYTE SURFACE MOLECULES [J].
KNAPP, W ;
RIEBER, P ;
DORKEN, B ;
SCHMIDT, RE ;
STEIN, H ;
VANDERBORNE, AEGK .
IMMUNOLOGY TODAY, 1989, 10 (08) :253-258
[43]   CLONING OF A LYMPHOCYTE HOMING RECEPTOR REVEALS A LECTIN DOMAIN [J].
LASKY, LA ;
SINGER, MS ;
YEDNOCK, TA ;
DOWBENKO, D ;
FENNIE, C ;
RODRIGUEZ, H ;
NGUYEN, T ;
STACHEL, S ;
ROSEN, SD .
CELL, 1989, 56 (06) :1045-1055
[44]   MECHANISMS OF LYMPHOCYTE ADHESION TO HUMAN VASCULAR ENDOTHELIAL-CELLS IN CULTURE - LYMPHOCYTE-T ADHESION TO ENDOTHELIAL-CELLS THROUGH ENDOTHELIAL HLA-DR ANTIGENS INDUCED BY GAMMA INTERFERON [J].
MASUYAMA, J ;
MINATO, N ;
KANO, S .
JOURNAL OF CLINICAL INVESTIGATION, 1986, 77 (05) :1596-1605
[45]   ADHESION OF LYMPHOCYTES-T TO HUMAN-ENDOTHELIAL CELLS IS REGULATED BY THE LFA-1 MEMBRANE MOLECULE [J].
MENTZER, SJ ;
BURAKOFF, SJ ;
FALLER, DV .
JOURNAL OF CELLULAR PHYSIOLOGY, 1986, 126 (02) :285-290
[46]  
MIOSSEC P, 1988, CLIN EXP IMMUNOL, V73, P250
[47]   CELL-CELL ADHESION MEDIATED BY CD8 AND MHC CLASS-I MOLECULES [J].
NORMENT, AM ;
SALTER, RD ;
PARHAM, P ;
ENGELHARD, VH ;
LITTMAN, DR .
NATURE, 1988, 336 (6194) :79-81
[48]   MIGRATION OF LYMPHOCYTES THROUGH ENDOTHELIAL-CELL MONOLAYERS - AUGMENTATION BY INTERFERON-GAMMA [J].
OPPENHEIMERMARKS, N ;
ZIFF, M .
CELLULAR IMMUNOLOGY, 1988, 114 (02) :307-323
[49]  
PALS ST, 1989, J IMMUNOL, V143, P851
[50]  
PALS ST, 1988, J IMMUNOL, V140, P1851