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首页> 外文期刊>Journal of Neurochemistry: Offical Journal of the International Society for Neurochemistry >F-actin cytoskeleton and the fate of organelles in chromaffin cells
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F-actin cytoskeleton and the fate of organelles in chromaffin cells

机译:F-肌动蛋白细胞骨架与嗜铬细胞中细胞器的命运

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In addition to playing a fundamental structural role, the F-actin cytoskeleton in neuroendocrine chromaffin cells has a prominent influence on governing the molecular mechanism and regulating the secretory process. Performing such roles, the F-actin network might be essential to first transport, and later locate the cellular organelles participating in the secretory cycle. Chromaffin granules are transported from the internal cytosolic regions to the cell periphery along microtubular and F-actin structures. Once in the cortical region, they are embedded in the F-actin network where these vesicles experience restrictions in motility. Similarly, mitochondria transport is affected by both microtubule and F-actin inhibitors and suffers increasing motion restrictions when they are located in the cortical region. Therefore, the F-actin cortex is a key factor in defining the existence of two populations of cortical and perinuclear granules and mitochondria which could be distinguished by their different location and mobility. Interestingly, other important organelles for controlling intracellular calcium levels, such as the endoplasmic reticulum network, present clear differences in distribution and much lower mobility than chromaffin vesicles and mitochondria. Nevertheless, both mitochondria and the endoplasmic reticulum appear to distribute in the proximity of secretory sites to fulfill a pivotal role, forming triads with calcium channels ensuring the fine tuning of the secretory response. This review presents the contributions that provide the basis for our current view regarding the influence that F-actin has on the distribution of organelles participating in the release of catecholamines in chromaffin cells, and summarizes this knowledge in simple models.
机译:除了发挥基本的结构作用外,神经内分泌嗜铬细胞中的F-肌动蛋白细胞骨架还对控制分子机制和调节分泌过程具有重要影响。扮演这样的角色,F-肌动蛋白网络可能是必不可少的,首先运输,然后定位参与分泌周期的细胞器。嗜铬粒蛋白颗粒沿着微管和F-肌动蛋白结构从内部胞质区域运输到细胞外围。一旦进入皮层区域,它们就会被嵌入F-肌动蛋白网络中,在这些网络中,这些囊泡会受到运动能力的限制。同样,线粒体运输受微管和F-肌动蛋白抑制剂的影响,并且当它们位于皮质区域时,运动受限性增加。因此,F-肌动蛋白皮质是确定存在两个皮质和核周颗粒和线粒体种群的关键因素,可以通过它们的不同位置和流动性来区分它们。有趣的是,其他控制细胞内钙水平的重要细胞器(例如内质网)呈现出明显的分布差异,并且迁移率比色氨酸囊泡和线粒体低得多。然而,线粒体和内质网似乎都分布在分泌部位附近,以发挥关键作用,形成具有钙通道的三联体,从而确保分泌反应的微调。这篇综述提出的贡献为我们当前关于F-肌动蛋白对参与嗜铬细胞中儿茶酚胺释放的细胞器分布的影响的观点提供了基础,并在简单模型中总结了这一知识。

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