PI3 kinase-dependent stimulation of platelet migration by stromal cell-derived factor 1 (SDF-1)

被引:75
作者
Kraemer, Bjoern F. [2 ]
Borst, Oliver [1 ,2 ]
Gehring, Eva-Maria [1 ]
Schoenberger, Tanja [2 ]
Urban, Benjamin [2 ]
Ninci, Elena [2 ]
Seizer, Peter [2 ]
Schmidt, Christine [2 ]
Bigalke, Boris [2 ]
Koch, Miriam [2 ]
Martinovic, Ivo [3 ]
Daub, Karin [2 ]
Merz, Tobias [4 ]
Schwanitz, Laura [2 ]
Stellos, Konstantinos [2 ]
Fiesel, Fabienne [5 ]
Schaller, Martin [6 ]
Lang, Florian [1 ]
Gawaz, Meinrad [2 ]
Lindemann, Stephan [2 ]
机构
[1] Univ Tubingen, Inst Physiol, D-72076 Tubingen, Germany
[2] Univ Klinikum Tubingen, Med Klin, Abt 3, D-72076 Tubingen, Germany
[3] Univ Marburg, Klin Herz & Thorakale Gefasschirurg, D-35037 Marburg, Germany
[4] Univ Tubingen, Nat Wissensch & Med Inst, D-72770 Reutlingen, Germany
[5] HERTIE Inst Klin Hirnforsch, Abt Neurodegenerat Erkrankungen, D-72076 Tubingen, Germany
[6] Univ Hautklin Tubingen, Haut Klin, D-72076 Tubingen, Germany
来源
JOURNAL OF MOLECULAR MEDICINE-JMM | 2010年 / 88卷 / 12期
关键词
Platelets; SDF-1; Cell migration; Cell signaling; Inflammation; ENDOTHELIAL PROGENITOR CELLS; TRANSENDOTHELIAL MIGRATION; PERTUSSIS-TOXIN; T-LYMPHOCYTES; CD34(+) CELLS; CHEMOKINE; ACTIVATION; CHEMOTAXIS; RECEPTORS; CXCR4;
D O I
10.1007/s00109-010-0680-8
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Platelets have been regarded as static cells that do not move once they adhere to a matrix. The present study explored, whether platelets are able to migrate. In contrast to the current opinion, we found that platelets were mobile, able to migrate over a surface, and transmigrate through a transwell membrane and endothelium toward a source of stromal cell-derived factor 1 (SDF-1). Platelet migration was stimulated by SDF-1, which led to the downstream activation and phosphorylation of Wiskott-Aldrich syndrome protein. SDF-1 signaling and subsequent platelet migration could be inhibited by CXCR4-receptor blocker AMD3100, pertussis toxin, inhibition of phosphoinositol 3-kinase (PI3 kinase) with LY294002 or wortmannin, and disruption of actin polymerization with cytochalasin B. The potential of platelets to migrate in an SDF-1-mediated fashion may redefine the role of platelets in the pathophysiology of vascular inflammation, subsequent atherosclerotic degeneration, and vascular regeneration.
引用
收藏
页码:1277 / 1288
页数:12
相关论文
共 34 条
[1]   The stromal cell-derived factor-1 chemokine is a potent platelet agonist highly expressed in atherosclerotic plaques [J].
Abi-Younes, S ;
Sauty, A ;
Mach, F ;
Sukhova, GK ;
Libby, P ;
Luster, AD .
CIRCULATION RESEARCH, 2000, 86 (02) :131-138
[2]  
BANGAHS, 1987, J BIOL CHEM, V262, P14871
[3]  
Berger G, 1998, BLOOD, V92, p347A
[4]   A highly efficacious lymphocyte chemoattractant, stromal cell-derived factor 1 (SDF-1) [J].
Bleul, CC ;
Fuhlbrigge, RC ;
Casasnovas, JM ;
Aiuti, A ;
Springer, TA .
JOURNAL OF EXPERIMENTAL MEDICINE, 1996, 184 (03) :1101-1109
[5]   PI-3-kinase and MAPK regulate mesangial cell proliferation and migration in response to PDGF [J].
Choudhury, GG ;
Karamitsos, C ;
Hernandez, J ;
Gentilini, A ;
Bardgette, J ;
Abboud, HE .
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY, 1997, 273 (06) :F931-F938
[6]  
Clemetson KJ, 2000, BLOOD, V96, P4046
[7]   Human platelets exhibit chemotaxis using functional N-formyl peptide receptors [J].
Czapiga, M ;
Gao, JL ;
Kirk, A ;
Lekstrom-Himes, J .
EXPERIMENTAL HEMATOLOGY, 2005, 33 (01) :73-84
[8]   Escaping the nuclear confines: Signal-dependent Pre-mRNA splicing in anucleate platelets [J].
Denis, MM ;
Tolley, ND ;
Bunting, M ;
Schwertz, H ;
Jiang, HM ;
Lindemann, S ;
Yost, CC ;
Rubner, FJ ;
Albertine, KH ;
Swoboda, KJ ;
Fratto, CM ;
Tolley, E ;
Kraiss, LW ;
McIntyre, TM ;
Zimmerman, GA ;
Weyrich, AS .
CELL, 2005, 122 (03) :379-391
[9]   Platelets exit venules by a transcellular pathway at sites of F-Met peptide-induced acute inflammation in guinea pigs [J].
Feng, D ;
Nagy, JA ;
Pyne, K ;
Dvorak, HF ;
Dvorak, AM .
INTERNATIONAL ARCHIVES OF ALLERGY AND IMMUNOLOGY, 1998, 116 (03) :188-195
[10]   Regulation of CXCR4-mediated chemotaxis and chemoinvasion of breast cancer cells [J].
Fernandis, AZ ;
Prasad, A ;
Band, H ;
Klösel, R ;
Ganju, RK .
ONCOGENE, 2004, 23 (01) :157-167