Department of Physiology, University of Wisconsin-Madison, Madison, Wisconsin, USA.
Biophys J. 2010 Mar 17;98(6):968-78. doi: 10.1016/j.bpj.2009.11.024.
Many synaptotagmins are Ca(2+)-binding membrane proteins with functions in Ca(2+)-triggered exocytosis. Synaptotagmin IV (syt IV) has no Ca(2+) binding activity, but nevertheless modulates exocytosis. Here, cell-attached capacitance recording was used to study single vesicle fusion and fission in control and syt IV overexpressing PC12 cells. Unitary capacitance steps varied widely in size, indicating that both microvesicles (MVs) and dense-core vesicles (DCVs) undergo fusion. Syt IV overexpression reduced the size of DCVs and endocytotic vesicles but not MVs. Syt IV also reduced the basal rate of Ca(2+)-induced fusion. During kiss-and-run, syt IV increased the conductance and duration of DCV fusion pores but not MV fusion pores. During full-fusion of DCVs syt IV increased the fusion pore conductance but not the duration. Syt IV overexpression increased the duration but not the conductance of fission pores during endocytosis. The effects of syt IV on fusion pores in PC12 cells resembled the effects on fusion pores in peptidergic nerve terminals. However, differences between these and results obtained with amperometry may indicate that amperometry and capacitance detect the fusion of different populations of vesicles. The effects of syt IV on fusion pores are discussed in terms of structural models and kinetic mechanisms.
许多突触结合蛋白是具有 Ca(2+)触发胞吐作用的 Ca(2+)结合膜蛋白。突触结合蛋白 IV(syt IV)没有 Ca(2+)结合活性,但仍然调节胞吐作用。在这里,使用细胞附着电容记录研究了对照和 syt IV 过表达 PC12 细胞中单囊泡融合和裂变。单位电容步的大小变化很大,表明微囊泡 (MVs) 和致密核心囊泡 (DCVs) 都发生融合。syt IV 过表达减小了 DCVs 和内吞小泡的大小,但不减小 MV。syt IV 还降低了 Ca(2+)诱导融合的基础速率。在 kiss-and-run 期间,syt IV 增加了 DCV 融合孔的电导和持续时间,但不增加 MV 融合孔的电导和持续时间。在 DCVs 的完全融合期间,syt IV 增加了融合孔的电导,但不增加其持续时间。syt IV 过表达增加了内吞过程中裂变孔的持续时间,但不增加其电导。syt IV 对 PC12 细胞融合孔的影响类似于对肽能神经末梢融合孔的影响。然而,这些与安培检测法结果之间的差异可能表明安培检测法和电容检测法检测到不同群体的囊泡融合。根据结构模型和动力学机制讨论了 syt IV 对融合孔的影响。