Receptor communication within the lymphocyte plasma membrane:: a role for the thrombospondin family of matricellular proteins

被引:17
作者
Forslow, A. [1 ]
Liu, Z. [1 ]
Sundqvist, K. -G. [1 ]
机构
[1] Karolinska Univ, Huddinge Hosp, Karolinska Inst, Div Clin Immunol,Dept Lab Med, SE-14186 Stockholm, Sweden
关键词
thrombospondin; lymphocyte; extracellular matrix; adhesion; integrin-associated protein; antigen-presenting cell;
D O I
10.1007/s00018-006-6255-8
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Lymphocytes, the principal cells of the immune system, carry out immune surveillance throughout the body by their unique capacity to constantly reposition themselves between a free-floating vascular state and a tissue state characterized by migration and frequent adhesive interactions with endothelial cells and components of the extracellular matrix. Therefore, mechanisms co-ordinating adhesion and migration with signals delivered through antigen recognition probably play a pivotal role for the regulation of lymphocyte behaviour and function. Endogenous thrombospondin-1 (TSP-1) seems to be the hub in such a mechanism for autocrine regulation of T cell adhesion and migration. TSP-1 functions as a mediator of cis interaction of vital receptors within the T lymphocyte plasma membrane, including integrins, low density lipoprotein receptor-related protein, calreticulin and integrin-associated protein.
引用
收藏
页码:66 / 76
页数:11
相关论文
共 126 条
[1]  
Adams J, 2004, INT J BIOCHEM CELL B, V36, P960, DOI 10.1016/j.biocel.2004.02.009
[2]   EXTRACELLULAR-MATRIX - THE THROMBOSPONDIN FAMILY [J].
ADAMS, J ;
LAWLER, J .
CURRENT BIOLOGY, 1993, 3 (03) :188-190
[3]  
ADAMS JC, 1993, J CELL SCI, V104, P1061
[4]   Thrombospondins: Multifunctional regulators of cell interactions [J].
Adams, JC .
ANNUAL REVIEW OF CELL AND DEVELOPMENTAL BIOLOGY, 2001, 17 :25-51
[5]  
Adams S, 1998, J IMMUNOL, V161, P1853
[6]   The lack of thrombospondin-1 (TSP1) dictates the course of wound healing in double-TSP1/TSP2-null mice [J].
Agah, A ;
Kyriakides, TR ;
Lawler, J ;
Bornstein, P .
AMERICAN JOURNAL OF PATHOLOGY, 2002, 161 (03) :831-839
[7]   THROMBOSPONDIN SEQUENCE MOTIF (CSVTCG) IS RESPONSIBLE FOR CD36-BINDING [J].
ASCH, AS ;
SILBIGER, S ;
HEIMER, E ;
NACHMAN, RL .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1992, 182 (03) :1208-1217
[8]   ANALYSIS OF CD36 BINDING DOMAINS - LIGAND SPECIFICITY CONTROLLED BY DEPHOSPHORYLATION OF AN ECTODOMAIN [J].
ASCH, AS ;
LIU, I ;
BRICCETTI, FM ;
BARNWELL, JW ;
KWAKYEBERKO, F ;
DOKUN, A ;
GOLDBERGER, J ;
PERNAMBUCO, M .
SCIENCE, 1993, 262 (5138) :1436-1440
[9]   Role of CD47 in the induction of human naive T cell anergy [J].
Avice, MN ;
Rubio, M ;
Sergerie, M ;
Delespesse, G ;
Sarfati, M .
JOURNAL OF IMMUNOLOGY, 2001, 167 (05) :2459-2468
[10]   Thrombospondin type 1 repeats interact with matrix metalloproteinase 2 - Regulation of metalloproteinase activity [J].
Bein, K ;
Simons, M .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (41) :32167-32173