首页> 外文期刊>The Journal of Neuroscience: The Official Journal of the Society for Neuroscience >F-actin and myosin II accelerate catecholamine release from chromaffin granules.
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F-actin and myosin II accelerate catecholamine release from chromaffin granules.

机译:F-肌动蛋白和肌球蛋白II加速儿茶酚胺从嗜铬菌素颗粒释放。

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摘要

The roles of nonmuscle myosin II and cortical actin filaments in chromaffin granule exocytosis were studied by confocal fluorescence microscopy, amperometry, and cell-attached capacitance measurements. Fluorescence imaging indicated decreased mobility of granules near the plasma membrane following inhibition of myosin II function with blebbistatin. Slower fusion pore expansion rates and longer fusion pore lifetimes were observed after inhibition of actin polymerization using cytochalasin D. Amperometric recordings revealed increased amperometric spike half-widths without change in quantal size after either myosin II inhibition or actin disruption. These results suggest that actin and myosin II facilitate release from individual chromaffin granules by accelerating dissociation of catecholamines from the intragranular matrix possibly through generation of mechanical forces.
机译:通过共聚焦荧光显微镜,安培法和细胞附着电容测量研究了肌无肌球蛋白II和皮质肌动蛋白丝在嗜铬粒细胞胞吐作用中的作用。荧光成像表明,用肌白蛋白抑制肌球蛋白II功能后,质膜附近颗粒的迁移率降低。使用细胞松弛素D抑制肌动蛋白聚合后,观察到较慢的融合孔扩展速率和更长的融合孔寿命。安培测量记录显示,肌球蛋白II抑制或肌动蛋白破坏后,安培峰的半峰宽度增加,而定量大小没有变化。这些结果表明肌动蛋白和肌球蛋白II可能通过产生机械力来促进儿茶酚胺从颗粒内基质中的解离,从而促进从各个嗜铬粒蛋白颗粒中释放。

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