Vav1 and Vav2 play different roles in macrophage migration and cytoskeletal organization

被引:33
作者
Wells, CM
Bhavsar, PJ
Evans, IR
Vigorito, E
Turner, M
Tybulewicz, V
Ridley, AJ
机构
[1] Royal Free & Univ Coll Med Sch, Med Sch Branch, Ludwig Inst Canc Res, London W1W 7BS, England
[2] UCL, Dept Biochem & Mol Biol, London, England
[3] UCL, MRC, Lab Mol Cell Biol, London, England
[4] UCL, Cell Biol Unit, London, England
[5] Babraham Inst, Lab Lymphocyte Signalling & Dev, Cambridge, England
[6] Natl Inst Med Res, Div Immune Cell Biol, London NW7 1AA, England
基金
英国生物技术与生命科学研究理事会; 英国医学研究理事会;
关键词
D O I
10.1016/j.yexcr.2005.07.015
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Vav family proteins act as guanine nucleotide exchange factors for Rho family proteins, which are known to orchestrate cytoskeletal changes and cell migration in response to extracellular stimuli. Using mice deficient for Vav1, Vav2 and/or Vav3, overlapping and isoform-specific functions of the three Vav proteins have been described in various hematopoietic cell types, but their roles in regulating cell morphology and migration have not been studied in detail. To investigate whether Vav isoforms have redundant or unique functions in regulating adhesion and migration, we investigated the properties of Vav1-deficient and Vav2-deficient macrophages. Both Vav1-deficient and Vav2-deficient cells have a smaller adhesive area; yet, only Vav1-deficient cells have a reduced migration speed, which coincides with a lower level of microtubules. Vav2-deficient inacrophages display a high level of constitutive membrane ruffling, but neither Vav1 nor Vav2 is required for colony stimulating factor-1-induced membrane ruffling and cell spreading. Our results suggest that the migration speed of macrophages is regulated independently of spread area or membrane ruffling and that Vav1 is selectively required to maintain a normal migration speed. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:303 / 310
页数:8
相关论文
共 53 条
[1]   Vav2 is an activator of Cdc42, Rac1, and RhoA [J].
Abe, K ;
Rossman, KL ;
Liu, B ;
Ritola, KD ;
Chiang, D ;
Campbell, SL ;
Burridge, K ;
Der, CJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (14) :10141-10149
[2]   Structural basis for relief of autoinhibition of the Dbl homology domain of proto-oncogene Vav by tyrosine phosphorylation [J].
Aghazadeh, B ;
Lowry, WE ;
Huang, XY ;
Rosen, MK .
CELL, 2000, 102 (05) :625-633
[3]   A role for Cdc42 in macrophage chemotaxis [J].
Allen, WE ;
Zicha, D ;
Ridley, AJ ;
Jones, GE .
JOURNAL OF CELL BIOLOGY, 1998, 141 (05) :1147-1157
[4]  
Allen WE, 1997, J CELL SCI, V110, P707
[5]  
Amieva MR, 1999, J CELL SCI, V112, P111
[6]   Vav1 transduces TCR signals required for LFA-1 function and cell polarization at the immunological synapse [J].
Ardouin, L ;
Bracke, M ;
Mathiot, A ;
Pagakis, SN ;
Norton, T ;
Hogg, N ;
Tybulewicz, VLJ .
EUROPEAN JOURNAL OF IMMUNOLOGY, 2003, 33 (03) :790-797
[7]   Regulatory and signaling properties of the Vav family [J].
Bustelo, XR .
MOLECULAR AND CELLULAR BIOLOGY, 2000, 20 (05) :1461-1477
[8]   Thrombin receptor activation and integrin engagement stimulate tyrosine phosphorylation of the proto-oncogene product, p95(vav), in platelets [J].
Cichowski, K ;
Brugge, JS ;
Brass, LF .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (13) :7544-7550
[9]   Phosphotyrosine-dependent activation of Rac-1 GDP/GTP exchange by the vav proto-oncogene product [J].
Crespo, P ;
Schuebel, KE ;
Ostrom, AA ;
Gutkind, JS ;
Bustelo, XR .
NATURE, 1997, 385 (6612) :169-172
[10]   Rac2-deficient mice display perturbed T-cell distribution and chemotaxis, but only minor abnormalities in TH1 responses [J].
Croker, BA ;
Handman, E ;
Hayball, JD ;
Baldwin, TM ;
Voigt, V ;
Cluse, LA ;
Yang, FC ;
Williams, DA ;
Roberts, AW .
IMMUNOLOGY AND CELL BIOLOGY, 2002, 80 (03) :231-240