首页> 外文期刊>Developmental cell >Vangl2 promotes Wnt/planar cell polarity-like signaling by antagonizing Dvl1-mediated feedback inhibition in growth cone guidance.
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Vangl2 promotes Wnt/planar cell polarity-like signaling by antagonizing Dvl1-mediated feedback inhibition in growth cone guidance.

机译:Vangl2通过拮抗在生长锥引导中的Dvl1介导的反馈抑制作用来促进Wnt /平面细胞极性样信号传导。

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Although a growing body of evidence supports that Wnt-Frizzled signaling controls axon guidance from vertebrates to worms, whether and how this is mediated by planar cell polarity (PCP) signaling remain elusive. We show here that the core PCP components are required for Wnt5a-stimulated outgrowth and anterior-posterior guidance of commissural axons. Dishevelled1 can inhibit PCP signaling by increasing hyperphosphorylation of Frizzled3 and preventing its internalization. Vangl2 antagonizes that by reducing Frizzled3 phosphorylation and promotes its internalization. In commissural axon growth cones, Vangl2 is predominantly localized on the plasma membrane and is highly enriched on the tips of the filopodia as well as in patches of membrane where new filopodia emerge. Taken together, we propose that the antagonistic functions of Vangl2 and Dvl1 (over Frizzled3 hyperphosphorylation and endocytosis) allow sharpening of PCP signaling locally on the tips of the filopodia to sense directional cues, Wnts, eventually causing turning of growth cones.
机译:尽管越来越多的证据支持Wnt-Frizzled信号控制着从脊椎动物到蠕虫的轴突导向,但是否以及如何由平面细胞极性(PCP)信号介导的轴突导向仍然难以捉摸。我们在这里显示核心的PCP组件是Wnt5a刺激的连合轴突的后向生长和前后引导所必需的。 Dishevelled1可以通过增加Frizzled3的过度磷酸化并阻止其内在化来抑制PCP信号传导。 Vangl2通过减少Frizzled3磷酸化来拮抗它,并促进其内在化。在连合轴突生长锥中,Vangl2主要定位在质膜上,并在丝状伪足的尖端以及新丝状伪足出现的膜片中高度富集。两者合计,我们建议Vangl2和Dvl1的拮抗作用(通过Frizzled3过度磷酸化和内吞作用)允许局部丝状伪足尖端上的PCP信号转导锐化,以感知方向提示,Wnt,最终引起生长视锥的转动。

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