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Repulsive Guidance Molecule a Inhibits Angiogenesis by Downregulating VEGF and Phosphorylated Focal Adhesion Kinase In Vitro

机译:排斥指导分子通过下调VEGF和磷酸化的局灶性粘附激酶在体外抑制血管生成。

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摘要

Repulsive guidance molecule a (RGMa) is a major neuron guidance factor in central nervous systems. We previously found that inhibition of RGMa could greatly enhance neural function rehabilitation in rats after MCAO/reperfusion. Neuron guidance factors are often regulators of angiogenesis. However, the effect of RGMa on angiogenesis and its mechanisms remain to be determined. Here, we investigated the effect of RGMa on endothelial cell (EC) proliferation, migration, tube formation, and cytoskeleton reassembly. The addition of recombinant RGMa significantly decreased the proliferation, migration, and tube formation of ECs. It also decreased the level of phosphorylated focal adhesion kinase (p-FAK Tyr397). Furthermore, the F-actin of the cytoskeleton assembly was obviously suppressed, with decreased filopodia and lamellipodia after the addition of RGMa. Knockout of neogenin or Unc5b significantly diminished RGMa’s inhibition of EC migration, tube formation, and cytoskeleton reassembly. RGMa-induced p-FAK (Tyr397) decrease was also abolished by knockout of neogenin or Unc5b. These results indicate that RGMa may be a negative regulator of angiogenesis through downregulating VEGF and p-FAK (Tyr397) via neogenin and Unc5b in vitro.
机译:排斥性指导分子a(RGMa)是中枢神经系统中的主要神经元指导因素。我们先前发现抑制RGMa可以大大增强MCAO /再灌注后大鼠的神经功能康复。神经元指导因子通常是血管生成的调节剂。然而,RGMa对血管生成及其机制的影响尚待确定。在这里,我们研究了RGMa对内皮细胞(EC)增殖,迁移,管形成和细胞骨架重组的影响。重组RGMa的加入显着降低了EC的增殖,迁移和管形成。它还降低了磷酸化粘着斑激酶(p-FAK Tyr397)的水平。此外,加入RGMa后,细胞骨架组装体的F-肌动蛋白受到明显抑制,丝状伪足和纤毛脂质减少。剔除新生成素或Unc5b大大降低了RGMa对EC迁移,管形成和细胞骨架重组的抑制作用。 RGMa诱导的p-FAK(Tyr397)的减少也被新蛋白或Unc5b的敲除所消除。这些结果表明,RGMa可能是通过新生蛋白和Unc5b在体外下调VEGF和p-FAK(Tyr397)而成为血管生成的负调节剂。

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