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Push-and-pull regulation of the fusion pore by synaptotagmin-7.


ABSTRACT: In chromaffin cells, Ca(2+) binding to synaptotagmin-1 and -7 triggers exocytosis by promoting fusion pore opening and fusion pore expansion. Synaptotagmins contain two C2 domains that both bind Ca(2+) and contribute to exocytosis; however, it remains unknown whether the C2 domains act similarly or differentially to promote opening and expansion of fusion pores. Here, we use patch amperometry measurements in WT and synaptotagmin-7-mutant chromaffin cells to analyze the role of Ca(2+) binding to the two synaptotagmin-7 C2 domains in exocytosis. We show that, surprisingly, Ca(2+) binding to the C2A domain suffices to trigger fusion pore opening but that the resulting fusion pores are unstable and collapse, causing a dramatic increase in kiss-and-run fusion events. Thus, synaptotagmin-7 controls fusion pore dynamics during exocytosis via a push-and-pull mechanism in which Ca(2+) binding to both C2 domains promotes fusion pore opening, but the C2B domain is selectively essential for continuous expansion of an otherwise unstable fusion pore.

SUBMITTER: Segovia M 

PROVIDER: S-EPMC2973888 | biostudies-other | 2010 Nov

REPOSITORIES: biostudies-other

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Push-and-pull regulation of the fusion pore by synaptotagmin-7.

Segovia Margarita M   Alés Eva E   Montes María Angeles MA   Bonifas Imelda I   Jemal Imane I   Lindau Manfred M   Maximov Anton A   Südhof Thomas C TC   Alvarez de Toledo Guillermo G  

Proceedings of the National Academy of Sciences of the United States of America 20101018 44


In chromaffin cells, Ca(2+) binding to synaptotagmin-1 and -7 triggers exocytosis by promoting fusion pore opening and fusion pore expansion. Synaptotagmins contain two C2 domains that both bind Ca(2+) and contribute to exocytosis; however, it remains unknown whether the C2 domains act similarly or differentially to promote opening and expansion of fusion pores. Here, we use patch amperometry measurements in WT and synaptotagmin-7-mutant chromaffin cells to analyze the role of Ca(2+) binding to  ...[more]

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