Getting to the site of inflammation: the leukocyte adhesion cascade updated

被引:3158
作者
Ley, Klaus [1 ]
Laudanna, Carlo
Cybulsky, Myron I.
Nourshargh, Sussan
机构
[1] Univ Virginia, Robert M Berne Cardiovasc Res Ctr, Charlottesville, VA 22908 USA
[2] Univ Virginia, Dept Biomed Engn, Charlottesville, VA 22908 USA
[3] Univ Virginia, Dept Mol Physiol, Charlottesville, VA 22908 USA
[4] Univ Virginia, Dept Biol Phys, Charlottesville, VA 22908 USA
[5] Univ Verona, Dept Pathol, I-37134 Verona, Italy
[6] Univ Verona, Dept Pathol, I-37134 Verona, Italy
[7] Univ Verona, Ctr Biomed Comp, I-37134 Verona, Italy
[8] Univ Toronto, Toronto Gen Res Inst, Toronto, ON M5G 1L7, Canada
[9] Univ Toronto, Dept Lab Med & Pathobiol, Toronto, ON M5G 1L7, Canada
[10] William Harvey Res Inst, Ctr Microvasc Res, London EC1M 68Q, England
基金
英国惠康基金;
关键词
D O I
10.1038/nri2156
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Neutrophil recruitment, lymphocyte recirculation and monocyte trafficking all require adhesion and transmigration through blood-vessel walls. The traditional three steps of rolling, activation and firm adhesion have recently been augmented and refined. Slow rolling, adhesion strengthening, intraluminal crawling and paracellular and transcellular migration are now recognized as separate, additional steps. In neutrophils, a second activation pathway has been discovered that does not require signalling through G-protein-coupled receptors and the signalling steps leading to integrin activation are beginning to emerge. This Review focuses on new aspects of one of the central paradigms of inflammation and immunity - the leukocyte adhesion cascade.
引用
收藏
页码:678 / 689
页数:12
相关论文
共 135 条
[71]   Binding of paxillin to α4 integrins modifies integrin-dependent biological responses [J].
Liu, S ;
Thomas, SM ;
Woodside, DG ;
Rose, DM ;
Kiosses, WB ;
Pfaff, M ;
Ginsberg, MH .
NATURE, 1999, 402 (6762) :676-681
[72]   A fragment of paxillin binds the α4 integrin cytoplasmic domain (tail) and selectively inhibits α4-mediated cell migration [J].
Liu, SC ;
Kiosses, WB ;
Rose, DM ;
Slepak, M ;
Salgia, R ;
Griffin, JD ;
Turner, CE ;
Schwartz, MA ;
Ginsberg, MH .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (23) :20887-20894
[73]   ENDOTHELIAL-LEUKOCYTE ADHESION MOLECULE-1 STIMULATES THE ADHESIVE ACTIVITY OF LEUKOCYTE INTEGRIN CR3 (CD11B CD18, MAC-1, ALPHA-M-BETA-2) ON HUMAN NEUTROPHILS [J].
LO, SK ;
LEE, S ;
RAMOS, RA ;
LOBB, R ;
ROSA, M ;
CHIROSSO, G ;
WRIGHT, SD .
JOURNAL OF EXPERIMENTAL MEDICINE, 1991, 173 (06) :1493-1500
[74]   CD99 is a key mediator of the transendothelial migration of neutrophils [J].
Lou, Olivia ;
Alcaide, Pilar ;
Luscinskas, Francis W. ;
Muller, William A. .
JOURNAL OF IMMUNOLOGY, 2007, 178 (02) :1136-1143
[75]   The alpha(1,3)Fucosyltransferase Fuc-TVII controls leukocyte trafficking through an essential role in L-, E-, and P-selectin ligand biosynthesis [J].
Maly, P ;
Thall, AD ;
Petryniak, B ;
Rogers, GE ;
Smith, PL ;
Marks, RM ;
Kelly, RJ ;
Gersten, KM ;
Cheng, GY ;
Saunders, TL ;
Camper, SA ;
Camphausen, RT ;
Sullivan, FX ;
Isogai, Y ;
Hindsgaul, O ;
vonAndrian, UH ;
Lowe, JB .
CELL, 1996, 86 (04) :643-653
[76]   Targeted recycling of PECAM from endothelial surface-connected compartments during diapedesis [J].
Mamdouh, Z ;
Chen, X ;
Pierini, LM ;
Maxfield, FR ;
Muller, WA .
NATURE, 2003, 421 (6924) :748-753
[77]   Direct observation of catch bonds involving cell-adhesion molecules [J].
Marshall, BT ;
Long, M ;
Piper, JW ;
Yago, T ;
McEver, RP ;
Zhu, C .
NATURE, 2003, 423 (6936) :190-193
[78]   Role of PSGL-1 binding to selectins in leukocyte recruitment [J].
McEver, RP ;
Cummings, RD .
JOURNAL OF CLINICAL INVESTIGATION, 1997, 100 (03) :485-492
[79]   Transcytosis and surface presentation of IL-8 ky venular endothelial cells [J].
Middleton, J ;
Neil, S ;
Wintle, J ;
ClarkLewis, I ;
Moore, H ;
Lam, C ;
Auer, M ;
Hub, E ;
Rot, A .
CELL, 1997, 91 (03) :385-395
[80]   Lymphocyte transcellular migration occurs through recruitment of endothelial ICAM-1 to caveola- and F-actin-rich domains [J].
Millán, J ;
Hewlett, L ;
Glyn, M ;
Toomre, D ;
Clark, P ;
Ridley, AJ .
NATURE CELL BIOLOGY, 2006, 8 (02) :113-U5