JAM family and related proteins in leukocyte migration (Vestweber series)

被引：86

作者：

Bradfield, Paul F.

Nourshargh, Sussan

Aurrand-Lions, Michel

Imhof, Beat A.

机构：

[1] Univ Geneva, Ctr Med, Dept Pathol & Immunol, CH-1211 Geneva 4, Switzerland

[2] Imperial Coll London, Cardiovasc Med Unit, Natl Heart & Lung Inst, Fac Med, London, England

来源：

ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY | 2007年 / 27卷 / 10期

关键词：

endothelium; leukocyte; transmigration; inflammation;

D O I：

10.1161/ATVBAHA.107.147694

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

Exploring the role of junctional adhesion molecules (JAMs) has proven to be varied and controversial. The purpose of this review is to discuss the new and exciting roles of these IgSF molecules and how they have evolved to contribute to diverse functions from development to inflammation. In particular, recent research has focused on JAM subfamily members JAM-A, -B, and -C with newly described roles in leukocyte trafficking during inflammation and angiogenesis. However, research on all JAM family members has demonstrated recurring themes with striking similarities in the many diverse processes they are now known to regulate.

引用

收藏

页码：2104 / 2112

页数：9

相关论文

共 100 条

[1] Cloning of human junctional adhesion molecule 3 (JAM3) and its identification as the JAM2 counter-receptor [J].

Arrate, MP ;

Rodriguez, JM ;

Tran, TM ;

Brock, TA ;

Cunningham, SA .

JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (49) :45826-45832

[2] Coxsackievirus and adenovirus receptor is essential for cardiomyocyte development [J].

Asher, DR ;

Cerny, AM ;

Weiler, SR ;

Horner, JW ;

Keeler, ML ;

Neptune, MA ;

Jones, SN ;

Bronson, RT ;

DePinho, RA ;

Finberg, RW .

GENESIS, 2005, 42 (02) :77-85

[3] Junctional adhesion molecule-C regulates the early influx of leukocytes into tissues during inflammation [J].

Aurrand-Lions, M ;

Lamagna, C ;

Dangerfield, JP ;

Wang, SJ ;

Herrera, P ;

Nourshargh, S ;

Imhof, BA .

JOURNAL OF IMMUNOLOGY, 2005, 174 (10) :6406-6415

[4] Heterogeneity of endothelial junctions is reflected by differential expression and specific subcellular localization of the three JAM family members [J].

Aurrand-Lions, M ;

Johnson-Leger, C ;

Wong, C ;

Du Pasquier, L ;

Imhof, BA .

BLOOD, 2001, 98 (13) :3699-3707

[5] JAM-2, a novel immunoglobulin superfamily molecule, expressed by endothelial and lymphatic cells [J].

Aurrand-Lions, M ;

Duncan, L ;

Ballestrem, C ;

Imhof, BA .

JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (04) :2733-2741

[6] Junction adhesion molecule is a receptor for reovirus [J].

Barton, ES ;

Forrest, JC ;

Connolly, JL ;

Chappell, JD ;

Liu, Y ;

Schnell, FJ ;

Nusrat, A ;

Parkos, CA ;

Dermody, TS .

CELL, 2001, 104 (03) :441-451

[7] Endothelial cell-to-cell junctions: Molecular organization and role in vascular homeostasis [J].

Bazzoni, G ;

Dejana, E .

PHYSIOLOGICAL REVIEWS, 2004, 84 (03) :869-901

[8] The JAM family of junctional adhesion molecules [J].

Bazzoni, G .

CURRENT OPINION IN CELL BIOLOGY, 2003, 15 (05) :525-530

[9] Mouse CD99 participates in T-cell recruitment into inflamed skin [J].

Bixel, G ;

Kloep, S ;

Butz, S ;

Petri, B ;

Engelhardt, B ;

Vestweber, D .

BLOOD, 2004, 104 (10) :3205-3213

[10]

BRADFIELD PF, 2007, BLOOD

← 1 2 3 4 5 6 7 8 9 10 →