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活性调节神经突向外生长和对硫酸软骨素蛋白聚糖的引导。

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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:硫酸软骨素蛋白聚糖(CSPG)是中枢神经系统中细胞外基质的主要成分,可抑制中枢神经系统损伤后的轴突再生。 CSPG触发的神经元中的信号传导途径仍是未知之数。在这项研究中,使用特征明确的体外试验进行神经突增生和神经突引导,我们证明了肌球蛋白II在神经元对CSPG的反应中起主要作用。我们发现CSPGs增加了肌球蛋白II调节性轻链的磷酸化。 blebbistatin对肌球蛋白II活性的特异性抑制使生长的神经突穿过CSPG丰富的区域,并增加了在CSPG上生长的神经元的神经突长度。使用特定的基因敲低,我们证明了肌球蛋白IIA和IIB在这些过程中的选择性作用。延时显微镜和免疫细胞化学表明,CSPG还抑制细胞粘附和细胞扩散。抑制肌球蛋白II选择性地加速了神经突的发生,而没有改变细胞的粘附力并在CSPGs上扩散。

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