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首页> 外文期刊>Frontiers in Cellular Neuroscience >Sustained Exocytosis after Action Potential-Like Stimulation at Low Frequencies in Mouse Chromaffin Cells Depends on a Dynamin-Dependent Fast Endocytotic Process
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Sustained Exocytosis after Action Potential-Like Stimulation at Low Frequencies in Mouse Chromaffin Cells Depends on a Dynamin-Dependent Fast Endocytotic Process

机译:在小鼠嗜铬细胞中以低频率进行类似动作电位刺激后的持续胞吐作用取决于动力依赖的快速内吞过程

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摘要

Under basal conditions the action potential firing rate of adrenal chromaffin cells is lower than 0.5 Hz. The maintenance of the secretory response at such frequencies requires a continuous replenishment of releasable vesicles. However, the mechanism that allows such vesicle replenishment remains unclear. Here, using membrane capacitance measurements on mouse chromaffin cells, we studied the mechanism of replenishment of a group of vesicles released by a single action potential-like stimulus (AP_(ls)). The exocytosis triggered by AP_(ls)(ETAP) represents a fraction (40%) of the immediately releasable pool, a group of vesicles highly coupled to voltage dependent calcium channels. ETAP was replenished with a time constant of 0.73 ± 0.11 s, fast enough to maintain synchronous exocytosis at 0.2–0.5 Hz stimulation. Regarding the mechanism involved in rapid ETAP replenishment, we found that it depends on the ready releasable pool; indeed depletion of this vesicle pool significantly delays ETAP replenishment. On the other hand, ETAP replenishment also correlates with a dynamin-dependent fast endocytosis process (τ = 0.53 ± 0.01 s). In this regard, disruption of dynamin function markedly inhibits the fast endocytosis and delays ETAP replenishment, but also significantly decreases the synchronous exocytosis during repetitive AP_(ls)stimulation at low frequencies (0.2 and 0.5 Hz). Considering these findings, we propose a model in where both the transfer of vesicles from ready releasable pool and fast endocytosis allow rapid ETAP replenishment during low stimulation frequencies.
机译:在基础条件下,肾上腺嗜铬细胞的动作电位激发速率低于0.5 Hz。要维持这种频率的分泌反应,就需要连续补充可释放的囊泡。但是,允许这种囊泡补充的机制仍不清楚。在这里,使用对小鼠嗜铬细胞的膜电容测量,我们研究了由单个动作电位样刺激(AP_(ls))释放的一组囊泡的补充机制。由AP_(Is)(ETAP)触发的胞吐作用代表立即释放池的一部分(40%),池是与电压依赖性钙通道高度偶联的一组囊泡。 ETAP的时间常数为0.73±0.11 s,足以在0.2-0.5 Hz刺激下保持同步胞吐作用。关于快速ETAP补给所涉及的机制,我们发现它取决于现成的可释放池。实际上,该囊泡池的耗竭明显延迟了ETAP的补给。另一方面,ETAP补充也与依赖于动力的快速内吞作用有关(τ= 0.53±0.01 s)。在这方面,动力蛋白功能的破坏明显抑制了快速的内吞作用并延迟了ETAP的补充,但在低频(0.2和0.5 Hz)的重复AP_(ls)刺激过程中,也显着降低了同步胞吐作用。考虑到这些发现,我们提出了一个模型,在该模型中,从可释放池的囊泡转移和快速内吞作用均允许在低刺激频率下快速补充ETAP。

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