Voets T, Neher E, Moser T
Department of Membrane Biophysics, Max-Planck-Institute for Biophysical Chemistry, Göttingen, Federal Republic of Germany.
Neuron. 1999 Jul;23(3):607-15. doi: 10.1016/s0896-6273(00)80812-0.
Many neurosecretory preparations display two components of depolarization-induced exocytosis: a phasic component synchronized with Ca2+ channel opening, followed by a slower sustained component. We evaluated possible mechanisms underlying this biphasic behavior by stimulating mouse chromaffin cells in situ with both depolarizations and flash photolysis of caged Ca2+. From a direct comparison of the secretory responses to both stimuli, we conclude that phasic and sustained release components originate from a readily releasable pool (RRP) of equally fusion-competent vesicles, suggesting that differences in the vesicles' proximity to Ca2+ channels underlie the biphasic secretory behavior. An intermediate pool in dynamic equilibrium with the RRP ensures rapid recruitment of release-ready vesicles after RRP depletion. Our results are discussed in terms of a refined model for secretion in chromaffin cells.
一个与Ca2+通道开放同步的相性组分,随后是一个较慢的持续性组分。我们通过对笼锁Ca2+进行去极化和闪光光解来原位刺激小鼠嗜铬细胞,评估了这种双相行为背后的可能机制。通过对两种刺激的分泌反应进行直接比较,我们得出结论,相性和持续性释放组分源自具有同等融合能力的囊泡的易释放池(RRP),这表明囊泡与Ca2+通道的接近程度差异是双相分泌行为的基础。与RRP处于动态平衡的中间池可确保RRP耗尽后快速募集准备好释放的囊泡。我们根据嗜铬细胞分泌的改进模型对结果进行了讨论。