P-selectin cell adhesion molecule in inflammation, thrombosis, cancer growth and metastasis

被引:86
作者
Geng, JG [1 ]
Chen, M
Chou, KC
机构
[1] Univ Minnesota, Sch Med, Vasc Biol Ctr, Minneapolis, MN 55455 USA
[2] Univ Minnesota, Sch Med, Div Hematol Oncol & Transplantat, Minneapolis, MN 55455 USA
[3] Chinese Acad Sci, Shanghai Inst Biol Sci, Inst Biochem & Cell Biol, Mol Cell Biol Lab, Shanghai 200031, Peoples R China
[4] Tianjin Inst Bioinformat & Drug Discovery, Tianjin 300074, Peoples R China
[5] Shanghai Jiao Tong Univ, Life Sci Res Ctr, Shanghai 200030, Peoples R China
[6] Gordon Life Sci Inst, San Diego, CA 92130 USA
关键词
selectin; cell adhesion molecule; leukocyte; platelet; endothelial cell; cancer cell; inflammation; thrombosis; cancer growth and metastasis;
D O I
10.2174/0929867043364720
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
P-selectin (CD62P) is a member of the selectin family of cell adhesion molecules. It is expressed on stimulated endothelial cells and activated platelets and mediates leukocyte rolling on stimulated endothelial cells and heterotypic aggregation of activated platelets onto leukocytes. It also mediates heterotypic aggregation of activated platelets to cancer cells and adhesion of cancer cells to stimulated endothelial cells. Using P-selectin knockout mice, the importance of P-selectin-mediated cell adhesive interactions in the pathogeneses of inflammation, thrombosis, growth and metastasis of cancers has been clearly demonstrated. Here we will summarize the current knowledge and highlight the important progress in the biomedical research of P-selectin biology, providing a suitable target for therapeutic interventions developed through both experimental and bioinformatic approaches.
引用
收藏
页码:2153 / 2160
页数:8
相关论文
共 96 条
[11]   Prediction of the tertiary structure of the complement control protein module [J].
Chou, KC ;
Heinrikson, RL .
JOURNAL OF PROTEIN CHEMISTRY, 1997, 16 (08) :765-773
[12]   THE CONVERGENCE-DIVERGENCE DUALITY IN LECTIN DOMAINS OF SELECTIN FAMILY AND ITS IMPLICATIONS [J].
CHOU, KC .
FEBS LETTERS, 1995, 363 (1-2) :123-126
[13]   Knowledge-based model building of the tertiary structures for lectin domains of the selectin family [J].
Chou, KC .
JOURNAL OF PROTEIN CHEMISTRY, 1996, 15 (02) :161-168
[14]   Chemokines - Chemokines and cell migration in secondary lymphoid organs [J].
Cyster, JG .
SCIENCE, 1999, 286 (5447) :2098-2102
[15]   Thrombin promotes platelet-mediated melanoma cell adhesion to endothelial cells under flow conditions: role of platelet glycoproteins P-selectin and GPIIb-IIIA [J].
Dardik, R ;
Savion, N ;
Kaufmann, Y ;
Varon, D .
BRITISH JOURNAL OF CANCER, 1998, 77 (12) :2069-2075
[16]   MECHANISMS OF LEUKOCYTE MOTILITY AND CHEMOTAXIS [J].
DOWNEY, GP .
CURRENT OPINION IN IMMUNOLOGY, 1994, 6 (01) :113-124
[17]   Anti-P-selectin antibody decreases inflammation and thrombus formation in venous thrombosis [J].
Downing, LJ ;
Wakefield, TW ;
Strieter, RM ;
Prince, MR ;
Londy, FJ ;
Fowlkes, JB ;
Hulin, MS ;
Kadell, AM ;
Wilke, CA ;
Brown, SL ;
Wrobleski, SK ;
Burdick, MD ;
Anderson, DC ;
Greenfield, LJ .
JOURNAL OF VASCULAR SURGERY, 1997, 25 (05) :816-827
[18]   CHARACTERIZATION OF GMP-140 (P-SELECTIN) AS A CIRCULATING PLASMA-PROTEIN [J].
DUNLOP, LC ;
SKINNER, MP ;
BENDALL, LJ ;
FAVALORO, EJ ;
CASTALDI, PA ;
GORMAN, JJ ;
GAMBLE, JR ;
VADAS, MA ;
BERNDT, MC .
JOURNAL OF EXPERIMENTAL MEDICINE, 1992, 175 (04) :1147-1150
[19]   Accumulation of tissue factor into developing thrombi in vivo is dependent upon microparticle P-selectin glycoprotein ligand 1 and platelet P-selectin [J].
Falati, S ;
Liu, QD ;
Gross, P ;
Merrill-Skoloff, G ;
Chou, J ;
Vandendries, E ;
Celi, A ;
Croce, K ;
Furie, BC ;
Furie, B .
JOURNAL OF EXPERIMENTAL MEDICINE, 2003, 197 (11) :1585-1598
[20]   Proteins of the exocytotic core complex mediate platelet α-granule secretion -: Roles of vesicle-associated membrane protein, SNAP-23, and syntaxin 4 [J].
Flaumenhaft, R ;
Croce, K ;
Chen, E ;
Furie, B ;
Furie, BC .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (04) :2492-2501