Intercellular adhesion molecule-1 (ICAM-1) expression and cell signaling cascades

被引:527
作者
Hubbard, AK
Rothlein, R
机构
[1] Univ Connecticut, Sch Pharm, Dept Pharmaceut Sci, Storrs, CT 06269 USA
[2] Boehringer Ingelheim Pharmaceut Inc, Dept Immunol, Ridgefield, CT 06877 USA
关键词
ICAM-1; cell signaling pathways; free radical;
D O I
10.1016/S0891-5849(00)00223-9
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
The collective interaction between cells is, in part, mediated by different families of adhesion molecules. Intercellular adhesion molecules (ICAMs) are structurally related members of the immunoglobulin supergene family and are ligands for the beta 2 integrin molecules present on leukocytes. Of the five ICAMs identified, ICAM-1 is the most extensively studied. Although ICAM-1 is expressed constitutively at low levels on endothelial cells and on some lymphocytes and monocytes, its expression can be significantly increased in the presence of cytokines (TNF alpha, IL-1, IFN gamma) and reactive oxygen species. Depending upon cell type, ICAM-1 participates in trafficking of inflammatory cells, in cell:cell interactions during antigen presentation, in microbial pathogenesis, and in signal transduction through outside-in signaling events. Again, depending upon cell type examined, ICAM-1 engagement has been documented to activate specific kinases through phosphorylation, resulting in transcription factor activation and increased cytokine production, increased cell membrane protein expression, reactive oxygen species production, and cell proliferation. (C) 2000 Elsevier Science Inc.
引用
收藏
页码:1379 / 1386
页数:8
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