Silence of Synaptotagmin VII inhibits release of dense core vesicles in PC12 cells.

JiangLi Li, Yang Xiao, Wei Zhou, ZhengXing Wu, RongYing Zhang, Tao Xu
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引用次数: 10

Abstract

Synaptotagmin VII (Syt VII), which has a higher Ca(2+) affinity and slower disassembly kinetics with lipid than Syt I and Syt IX, was regarded as being uninvolved in synaptic vesicle (SV) exocytosis but instead possibly as a calcium sensor for the slower kinetic phase of dense core vesicles (DCVs) release. By using high temporal resolution capacitance and amperometry measurements, it was demonstrated that the knockdown of endogenous Syt VII attenuated the fusion of DCV with the plasma membrane, reduced the amplitude of the exocytotic burst of the Ca(2+)-triggered DCV release without affecting the slope of the sustained component, and blocked the fusion pore expansion. This suggests that Syt VII is the Ca(2+) sensor of DCV fusion machinery and is an essential factor for the establishment and maintenance of the pool size of releasable DCVs in PC12 cells.

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Synaptotagmin VII沉默抑制PC12细胞致密核囊泡的释放。
Synaptotagmin VII (Syt VII)具有比Syt I和Syt IX更高的Ca(2+)亲和力和更慢的脂质分解动力学,被认为与突触囊泡(SV)胞外作用无关,而可能是致密核心囊泡(DCVs)释放较慢动力学阶段的钙传感器。通过高时间分辨率电容和安培测量,结果表明,内源性Syt 7的敲低减弱了DCV与质膜的融合,降低了Ca(2+)触发的DCV释放的胞外爆发幅度,而不影响持续组分的斜率,并阻断了融合孔的扩张。这表明Syt VII是DCV融合机制的Ca(2+)传感器,是PC12细胞中可释放DCV池大小建立和维持的重要因素。
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