β2 Integrin signaling in leukocytes

被引:46
作者
Dib, K [1 ]
Andersson, T [1 ]
机构
[1] Lund Univ, Malmo Univ Hosp, Dept Lab Med, Div Expt Pathol, SE-20502 Malmo, Sweden
来源
FRONTIERS IN BIOSCIENCE-LANDMARK | 2000年 / 5卷
关键词
beta; 2; integrins; leukocytes; cytoskeleton; small GTPases; tyrosine kinases; Ca2+; review;
D O I
10.2741/Pathology
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
Members of the beta 2 integrin family are the dominating integrins expressed on leukocytes, and they play a major role in leukocyte cell-cell and cell-matrix adhesions during inflammation and other immune responses. beta 2 integrins are signaling receptors, but they are also targets of and are functionally affected by intracellular signals. Accordingly, researchers usually discuss two types of signaling by beta 2 integrins (and integrins in general): transmission of signals into the cell following binding of ligands or counter-receptors to the integrins (outside-in signaling), and regulation of the avidity and conformation of integrins by signals generated by other receptors within the cell (inside-out signaling). In this review, our aim is to summarize what is known about the capacity of beta 2 integrins to generate outside-in signaling in leukocytes, in particular polymorphonuclear neutrophils. Results in the literature clearly demonstrate that one of the earliest events in beta 2 integrin signaling is activation of non-receptor tyrosine kinases, which in turn triggers downstream activation of various signaling pathways that affect different functional responses of the cell. We also discuss molecules of potential importance in beta 2 integrin signaling.
引用
收藏
页码:D438 / D451
页数:14
相关论文
共 132 条
[1]   REGULATED CA2+ SIGNALING THROUGH LEUKOCYTE CD11B/CD18 INTEGRIN [J].
ALTIERI, DC ;
STAMNES, SJ ;
GAHMBERG, CG .
BIOCHEMICAL JOURNAL, 1992, 288 :465-473
[2]   The Cbl proto-oncogene product negatively regulates the Src-family tyrosine kinase Fyn by enhancing its degradation [J].
Andoniou, CE ;
Lill, NL ;
Thien, CB ;
Lupher, ML ;
Ota, S ;
Bowtell, DDL ;
Scaife, RM ;
Langdon, WY ;
Band, H .
MOLECULAR AND CELLULAR BIOLOGY, 2000, 20 (03) :851-867
[3]  
Aplin AE, 1998, PHARMACOL REV, V50, P197
[4]  
ARNAOUT MA, 1990, BLOOD, V75, P1037
[5]  
AXELSSON LC, 2000, EXP CELL RES, V256
[6]   Negative regulation of lymphocyte activation and autoimmunity by the molecular adaptor Cbl-b [J].
Bachmaier, K ;
Krawczyk, C ;
Kozieradzki, I ;
Kong, YY ;
Sasaki, T ;
Oliveira-dos-Santos, A ;
Mariathasan, S ;
Bouchard, D ;
Wakeham, A ;
Itie, A ;
Le, J ;
Ohashi, PS ;
Sarosi, I ;
Nishina, H ;
Lipkowitz, S ;
Penninger, JM .
NATURE, 2000, 403 (6766) :211-216
[7]   Are changes in integrin affinity and conformation overemphasized? [J].
Bazzoni, G ;
Hemler, ME .
TRENDS IN BIOCHEMICAL SCIENCES, 1998, 23 (01) :30-34
[8]   Characterization of Rac and Cdc42 activation in chemoattractant-stimulated human neutrophils using a novel assay for active GTPases [J].
Benard, V ;
Bohl, BP ;
Bokoch, GM .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (19) :13198-13204
[9]   INOSITOL TRISPHOSPHATE AND CALCIUM SIGNALING [J].
BERRIDGE, MJ .
NATURE, 1993, 361 (6410) :315-325
[10]   Neutrophil activation by adhesion: Mechanisms and pathophysiological implications [J].
Berton, G ;
Yan, SR ;
Funagalli, L ;
Lowell, CA .
INTERNATIONAL JOURNAL OF CLINICAL & LABORATORY RESEARCH, 1996, 26 (03) :160-177