Phosphorylation of the endothelial nitric oxide synthase at Ser-1177 is required for VEGF-induced endothelial cell migration

被引:313
作者
Dimmeler, S [1 ]
Dernbach, E [1 ]
Zeiher, AM [1 ]
机构
[1] Goethe Univ Frankfurt, Dept Internal Med 4, D-60590 Frankfurt, Germany
关键词
migration; proliferation; protein kinase; nitric oxide; vascular endothelial growth factor;
D O I
10.1016/S0014-5793(00)01657-4
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
Vascular endothelial growth factor (VEGF) stimulates endothelial cell (EC) migration. The protein kinase Akt activates the endothelial NO synthase (eNOS) by phosphorylation of Ser-1177, Therefore, we investigated the contribution of Akt-mediated eNOS phosphorylation to VEGF-induced EC migration. Inhibition of NO synthase or overexpression of a dominant negative Akt abrogated VEGF-induced cell migration. In contrast, overexpression of constitutively active Akt was sufficient to induce cell migration. Moreover, transfection of an Akt site phospho-mimetic eNOS (S1177D) potently stimulated EC migration, whereas a non-phosphorylatable mutant (S1177A) inhibited VEGF-induced EC migration. Our data indicate that eNOS activation via phosphorylation of Ser-1177 by Akt is necessary and sufficient for VEGF-mediated EC migration. (C) 2000 Federation of European Biochemical Societies. Published by Elsevier Science B.V, All rights reserved.
引用
收藏
页码:258 / 262
页数:5
相关论文
共 21 条
  • [1] BROCK TA, 1991, AM J PATHOL, V138, P213
  • [2] Targeted deficiency or cytosolic truncation of the VE-cadherin gene in mice impairs VEGF-mediated endothelial survival and angiogenesis
    Carmeliet, P
    Lampugnani, MG
    Moons, L
    Breviario, F
    Compernolle, V
    Bono, F
    Balconi, G
    Spagnuolo, R
    Oosthuyse, B
    Dewerchin, M
    Zanetti, A
    Angellilo, A
    Mattot, V
    Nuyens, D
    Lutgens, E
    Clotman, F
    de Ruiter, MC
    Gittenberger-de Groot, A
    Poelmann, R
    Lupu, F
    Herbert, JM
    Collen, D
    Dejana, E
    [J]. CELL, 1999, 98 (02) : 147 - 157
  • [3] Akt takes center stage in angiogenesis signaling
    Dimmeler, S
    Zeiher, AM
    [J]. CIRCULATION RESEARCH, 2000, 86 (01) : 4 - 5
  • [4] Activation of nitric oxide synthase in endothelial cells by Akt-dependent phosphorylation
    Dimmeler, S
    Fleming, I
    Fisslthaler, B
    Hermann, C
    Busse, R
    Zeiher, AM
    [J]. NATURE, 1999, 399 (6736) : 601 - 605
  • [5] Fluid shear stress stimulates phosphorylation of Akt in human endothelial cells - Involvement in suppression of apoptosis
    Dimmeler, S
    Assmus, B
    Hermann, C
    Haendeler, J
    Zeiher, AM
    [J]. CIRCULATION RESEARCH, 1998, 83 (03) : 334 - 341
  • [6] Akt mediates cytoprotection of endothelial cells by vascular endothelial growth factor in an anchorage-dependent manner
    Fujio, Y
    Walsh, K
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (23) : 16349 - 16354
  • [7] Regulation of endothelium-derived nitric oxide production by the protein kinase Akt
    Fulton, D
    Gratton, JP
    McCabe, TJ
    Fontana, J
    Fujio, Y
    Walsh, K
    Franke, TF
    Papapetropoulos, A
    Sessa, WC
    [J]. NATURE, 1999, 399 (6736) : 597 - 601
  • [8] Vascular endothelial growth factor regulates endothelial cell survival through the phosphatidylinositol 3′-kinase Akt signal transduction pathway -: Requirement for Flk-1/KDR activation
    Gerber, HP
    McMurtrey, A
    Kowalski, J
    Yan, MH
    Keyt, BA
    Dixit, V
    Ferrara, N
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (46) : 30336 - 30343
  • [9] Hood JD, 1998, AM J PHYSIOL-HEART C, V274, pH1054
  • [10] Angiogenesis and vasculogenesis as therapeutic strategies for postnatal neovascularization
    Isner, JM
    Asahara, T
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1999, 103 (09) : 1231 - 1236