Thrower Edwin C, Park Hee Yun, So Seung Ho, Yoo Seung Hyun, Ehrlich Barbara E
Department of Pharmacology, Yale University, New Haven, Connecticut 06520, USA.
J Biol Chem. 2002 May 3;277(18):15801-6. doi: 10.1074/jbc.M110139200. Epub 2002 Feb 12.
Secretory granules of neuroendocrine cells are inositol 1,4,5-trisphosphate (InsP(3))-sensitive Ca(2+) stores in which the Ca(2+) storage protein, chromogranin A (CGA), couples with InsP(3)-gated Ca(2+) channels (InsP(3)R) located in the granule membrane. The functional aspect of this coupling has been investigated via release studies and planar lipid bilayer experiments in the presence and absence of CGA. CGA drastically increased the release activity of the InsP(3)R by increasing the channel open probability by 9-fold and the mean open time by 12-fold. Our results show that CGA-coupled InsP(3)Rs are more sensitive to activation than uncoupled receptors. This modulation of InsP(3)R channel activity by CGA appears to be an essential component in the control of intracellular Ca(2+) concentration by secretory granules and may regulate the rate of vesicle fusion and exocytosis.
神经内分泌细胞的分泌颗粒是对肌醇1,4,5-三磷酸(InsP(3))敏感的钙库,其中钙储存蛋白嗜铬粒蛋白A(CGA)与位于颗粒膜上的InsP(3)门控钙通道(InsP(3)R)偶联。这种偶联的功能方面已通过在有和没有CGA的情况下进行的释放研究和平面脂质双层实验进行了研究。CGA通过将通道开放概率提高9倍和平均开放时间提高12倍,极大地增加了InsP(3)R的释放活性。我们的结果表明,与CGA偶联的InsP(3)R比未偶联的受体对激活更敏感。CGA对InsP(3)R通道活性的这种调节似乎是分泌颗粒控制细胞内钙浓度的一个重要组成部分,并且可能调节囊泡融合和胞吐作用的速率。