VEGF165的肝素结合域直接与整合素αvβ3结合,在信号传导中起关键作用。

Yoko K Takada, Jessica Yu, Xiaojin Ye, Chun-Yi Wu, Brunie H Felding, Masaaki Fujita, yoshikazu takada
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引用次数: 0

摘要

VEGF-A是肿瘤血管生成的关键细胞因子,也是肿瘤的主要治疗靶点。VEGF165是主要的异构体,是最有效的血管生成兴奋剂。VEGFR2/KDR结构域2和3 (D2D3)与VEGF165的n端结构域(NTD,残基1-110)结合。由于去除肝素结合结构域(HBD,残基111-165)显著降低了VEGF165的有丝分裂活性,因此有人提出HBD在VEGF165的有丝分裂性中起关键作用。整合素αvβ3已被证实与VEGF165结合,但整合素αvβ3在VEGF165信号传导中的作用尚不清楚。在这里,我们描述了αvβ3特异性结合到分离的HBD,而不是NTD。通过对接模拟和诱变,我们确定了HBD中整合素结合的几个关键氨基酸残基(Arg-123、Arg-124、Lys-125、Lys-140、Arg-145和Arg-149),并通过在HBD中加入突变,生成了全长的整合素结合缺陷VEGF165。全长突变体VEGF165整合素结合缺陷(R123A/R124A/K125A/K140A/R145A/R149A)在ERK1/2磷酸化、整合素β3磷酸化和KDR磷酸化方面存在缺陷,尽管该突变不影响KDR与VEGF165的结合。我们提出了一个模型,其中VEGF165诱导KDR(通过NTD)-VEGF165(通过HBD)-整合素αvβ3三元复合物在细胞表面形成,这一过程对VEGF165的强有丝分裂性至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The heparin-binding domain of VEGF165 directly binds to integrin αvβ3 and plays a critical role in signaling.
VEGF-A is a key cytokine in tumor angiogenesis and a major therapeutic target for cancer. VEGF165 is the predominant isoform and is the most potent angiogenesis stimulant. VEGFR2/KDR domains 2 and 3 (D2D3) bind to the N-terminal domain (NTD, residues 1-110) of VEGF165. Since removal of the heparin-binding domain (HBD, residues 111-165) markedly reduced the mitogenic activity of VEGF165, it has been proposed that the HBD plays a critical role in the mitogenicity of VEGF165. Integrin αvβ3 has been shown to bind to VEGF165, but the role of integrin αvβ3 in VEGF165 signaling are unclear. Here we describe that αvβ3 specifically bound to the isolated HBD, but not to the NTD. We identified several critical amino acid residues in HBD for integrin binding (Arg-123, Arg-124, Lys-125, Lys-140, Arg-145, and Arg-149) by docking simulation and mutagenesis, and generated full-length VEGF165 that is defective in integrin binding by including mutations in the HBD. The full-length VEGF165 mutant defective in integrin binding (R123A/R124A/K125A/K140A/R145A/R149A) was defective in ERK1/2 phosphorylation, integrin β3 phosphorylation, and KDR phosphorylation, although the mutation did not affect KDR binding to VEGF165. We propose a model in which VEGF165 induces KDR (through NTD)-VEGF165 (through HBD)-integrin αvβ3 ternary complex formation on the cell surface and this process is critically involved in potent mitogenicity of VEGF165.
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