首页> 外文期刊>Journal of Neurochemistry: Offical Journal of the International Society for Neurochemistry >Myosin II activity regulates neurite outgrowth and guidance in response to chondroitin sulfate proteoglycans.
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Myosin II activity regulates neurite outgrowth and guidance in response to chondroitin sulfate proteoglycans.

机译:肌球蛋白II活性调节神经突的出现和指导,以应对硫酸软骨素蛋白多糖蛋白多糖。

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摘要

Chondroitin sulfate proteoglycans (CSPGs) are major components of the extracellular matrix in the CNS that inhibit axonal regeneration after CNS injury. Signaling pathways in neurons triggered by CSPGs are still largely unknown. In this study, using well-characterized in vitro assays for neurite outgrowth and neurite guidance, we demonstrate a major role for myosin II in the response of neurons to CSPGs. We found that the phosphorylation of myosin II regulatory light chains is increased by CSPGs. Specific inhibition of myosin II activity with blebbistatin allows growing neurites to cross onto CSPG-rich areas and increases the length of neurites of neurons growing on CSPGs. Using specific gene knockdown, we demonstrate selective roles for myosin IIA and IIB in these processes. Time lapse microscopy and immunocytochemistry demonstrated that CSPGs also inhibit cell adhesion and cell spreading. Inhibition of myosin II selectively accelerated neurite initiation without altering cell adhesion and spreading on CSPGs.
机译:软骨素硫酸酯蛋白多糖(CSPG)是CNS损伤后抑制轴突再生的CNS细胞外基质的主要组分。 CSPG触发的神经元中的信号通路仍然很大程度上是未知的。在这项研究中,使用良好的体外测定的神经突血肿和神经突指导,我们对肌球蛋白II的主要作用表现出在神经元对CSPG的反应中。我们发现,CSPGs增加了肌霉素II调节性轻链的磷酸化。用Blebbistatin的肌蛋白II活性对肌球蛋白II活性的特异性抑制允许生长的神经毒素穿过CSPG的区域并增加神经元在CSPG上生长的神经脉的长度。使用特定的基因敲低,我们证明了在这些过程中的肌球蛋白IIA和IIB的选择性作用。时间流逝显微镜和免疫细胞化学证明CSPG也抑制细胞粘附和细胞扩散。抑制肌蛋白II选择性地加速神经沸石引发,而不改变细胞粘附并在CSPG上扩散。

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