Journal article
Triple Function of Synaptotagmin 7 Ensures Efficiency of High-Frequency Transmission at Central GABAergic Synapses
Cell reports (Cambridge), Vol.21(8), pp.2082-2089
11/21/2017
DOI: 10.1016/j.celrep.2017.10.122
PMCID: PMC5863544
PMID: 29166601
Abstract
Synaptotagmin 7 (Syt7) is thought to be a Ca2+ sensor that mediates asynchronous transmitter release and facilitation at synapses. However, Syt7 is strongly expressed in fast-spiking, parvalbumin-expressing GABAergic interneurons, and the output synapses of these neurons produce only minimal asynchronous release and show depression rather than facilitation. To resolve this apparent contradiction, we examined the effects of genetic elimination of Syt7 on synaptic transmission at the GABAergic basket cell (BC)-Purkinje cell (PC) synapse in cerebellum. Our results indicate that at the BC-PC synapse, Syt7 contributes to asynchronous release, pool replenishment, and facilitation. In combination, these three effects ensure efficient transmitter release during high-frequency activity and guarantee frequency independence of inhibition. Our results identify a distinct function of Syt7: ensuring the efficiency of high-frequency inhibitory synaptic transmission.
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•Syt7 contributes to asynchronous release, facilitation, and replenishment•Syt7 conveys efficient and frequency-independent release during repetitive activity•Syt7 enables the powerful control of PC activity by single BC synaptic inputs•Syt7 has similar functions at cerebellar and hippocampal BC synapses
Chen et al. demonstrate that synaptotagmin 7 at cerebellar inhibitory synapses functions as a Ca2+ sensor for asynchronous release, facilitation, and vesicle pool replenishment. This triple function of Syt7 ensures efficacy and frequency independence of inhibitory synaptic transmission.
Details
- Title: Subtitle
- Triple Function of Synaptotagmin 7 Ensures Efficiency of High-Frequency Transmission at Central GABAergic Synapses
- Creators
- Chong Chen - IST Austria (Institute of Science and Technology Austria), Am Campus 1, A-3400 Klosterneuburg, AustriaRachel Satterfield - Max Planck Florida Institute for Neuroscience, Research Group Molecular Mechanisms of Synaptic Function, Jupiter, FL 33458, USASamuel M Young - Max Planck Florida Institute for Neuroscience, Research Group Molecular Mechanisms of Synaptic Function, Jupiter, FL 33458, USAPeter Jonas - IST Austria (Institute of Science and Technology Austria), Am Campus 1, A-3400 Klosterneuburg, Austria
- Resource Type
- Journal article
- Publication Details
- Cell reports (Cambridge), Vol.21(8), pp.2082-2089
- DOI
- 10.1016/j.celrep.2017.10.122
- PMID
- 29166601
- PMCID
- PMC5863544
- NLM abbreviation
- Cell Rep
- ISSN
- 2211-1247
- eISSN
- 2211-1247
- Publisher
- Elsevier Inc
- Language
- English
- Date published
- 11/21/2017
- Academic Unit
- Anatomy and Cell Biology; Iowa Neuroscience Institute; Otolaryngology
- Record Identifier
- 9984025307402771
Metrics
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