Meyer Rosana D, Latz Catharina, Rahimi Nader
Departments of Ophthalmology and Biochemistry, Boston University School of Medicine, 715 Albany Street, Boston, MA 02118, USA.
J Biol Chem. 2003 May 2;278(18):16347-55. doi: 10.1074/jbc.M300259200. Epub 2003 Feb 21.
Vascular endothelial growth factor-mediated angiogenic signal transduction relay is achieved by coordinated induction of endothelial cell proliferation, migration, and differentiation. These complex cellular processes are most likely controlled by activation of both cooperative and antagonistic signals by vascular endothelial growth factor receptors (VEGFRs). Here, we investigated the contribution of tyrosine-phosphorylated residues of VEGFR-2/fetal liver kinase-1 to endothelial cell proliferation and differentiation and activation of signaling proteins. Mutation of tyrosine 1006 of VEGFR-2 to phenylalanine severely impaired the ability of this receptor to stimulate endothelial cell differentiation and tubulogenesis. Paradoxically, the mutant receptor stimulated endothelial cell proliferation far better than the wild-type receptor. Further analysis showed that tyrosine 1006 is responsible for phospholipase Cgamma1 (PLCgamma1) activation and intracellular calcium release in endothelial cells. Activation of PLCgamma1 was selectively mediated by tyrosine 1006. Mutation of tyrosines 799, 820, 949, 994, 1080, 1173, and 1221 had no measurable effect on the ability of VEGFR-2 to stimulate PLCgamma1 activation. Association of VEGFR-2 with PLCgamma1 was mainly established between tyrosine 1006 and the C-terminal SH2 domain of PLCgamma1 in vitro and in vivo. Taken together, the results indicate that phosphorylation of tyrosine 1006 is essential for VEGFR-2-mediated PLCgamma1 activation, calcium flux, and cell differentiation. More importantly, VEGFR-2-mediated endothelial cell proliferation is inversely correlated with the ability of VEGFR-2 to associate with and activate PLCgamma1.
血管内皮生长因子介导的血管生成信号转导中继是通过协调诱导内皮细胞增殖、迁移和分化来实现的。这些复杂的细胞过程很可能由血管内皮生长因子受体(VEGFRs)激活协同和拮抗信号来控制。在此,我们研究了VEGFR-2/胎儿肝激酶-1的酪氨酸磷酸化残基对内皮细胞增殖、分化以及信号蛋白激活的作用。将VEGFR-2的酪氨酸1006突变为苯丙氨酸严重损害了该受体刺激内皮细胞分化和形成管状结构的能力。矛盾的是,突变受体刺激内皮细胞增殖的能力远比野生型受体强。进一步分析表明,酪氨酸1006负责内皮细胞中磷脂酶Cγ1(PLCγ1)的激活和细胞内钙释放。PLCγ1的激活由酪氨酸1006选择性介导。酪氨酸799、820、949、994、1080、1173和1221的突变对VEGFR-2刺激PLCγ1激活的能力没有可测量的影响。在体外和体内,VEGFR-2与PLCγ1的结合主要在酪氨酸1006和PLCγ1的C末端SH2结构域之间建立。综上所述,结果表明酪氨酸1006的磷酸化对于VEGFR-2介导的PLCγ1激活、钙通量和细胞分化至关重要。更重要的是,VEGFR-2介导的内皮细胞增殖与VEGFR-2与PLCγ1结合并激活它的能力呈负相关。