Spatio-temporal regulation of neurotransmitter release by PKC; studies in adrenal chromaffin cells.

Konosuke Kumakura, Nobuyiki Sasakawa, Norie Murayama, Mica Ohara-Imaizumi
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引用次数: 8

Abstract

Activation of protein kinase C (PKC) seems to promote vesicle recruitment to the release-ready state prior to Ca2+ -triggered fusion in chromaffin cells. To understand spatio-temporal regulation of vesicle recruitment by PKC, we studied the effects of a phorbol ester, 12-O-tetradecanoylphorbol-13-acetate (TPA), on the vesicle movements in living chromaffin cells by imaging with a fluorescence microscope-cooled CCD system. About 60 approximately 80% of the chromaffin vesicles showed a rapid movement, about 20% showed a moderate movement, and the rest showed slow/no movement in resting and post-stimulation. The vesicles with slow/no movement increased to 40% upon a depolarizing stimulation, and TPA increased this population to about 70%. TPA treatment, in addition, increased the number of visible chromaffin vesicles beneath the plasma membrane, suggesting that the potentiation of vesicle recruitment by PKC involves a substantial increase in the subplasmalemmal distribution of vesicles.

PKC对神经递质释放的时空调控肾上腺染色质细胞的研究。
蛋白激酶C (PKC)的激活似乎在Ca2+触发的染色质细胞融合之前促进囊泡募集到释放准备状态。为了了解PKC对囊泡募集的时空调控,我们利用荧光显微镜冷却CCD成像系统研究了12- o-十四烷醇-13-乙酸磷酯(TPA)对活嗜铬细胞囊泡运动的影响。约60% - 80%的染色质囊泡在静息和刺激后表现为快速运动,约20%表现为中等运动,其余表现为缓慢或不运动。在去极化刺激下,运动缓慢或无运动的囊泡增加到40%,而TPA使这一群体增加到70%左右。此外,TPA处理增加了质膜下可见的染色质囊泡的数量,这表明PKC增强囊泡募集涉及到囊泡在质下分布的大量增加。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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