Local routes revisited: the space and time dependence of the Ca2+ signal for phasic transmitter release at the rat calyx of Held
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During the last decade, advances in experimental techniques and quantitative modelling have resulted in the development of the calyx of Held as one of the best preparations in which to study synaptic transmission. Here we review some of these advances, including simultaneous recording of pre- and postsynaptic currents, measuring the Ca2+ sensitivity of transmitter release, reconstructing the 3-D anatomy at the electron microscope (EM) level, and modelling the buffered diffusion of Ca2+ in the nerve terminal. An important outcome of these studies is an improved understanding of the Ca2+ signal that controls phasic transmitter release. This article illustrates the spatial and temporal aspects of the three main steps in the presynaptic signalling cascade: Ca2+ influx through voltage-gated calcium channels, buffered Ca2+ diffusion from the channels to releasable vesicles, and activation of the Ca2+ sensor for release. Particular emphasis is placed on how presynaptic Ca2+ buffers affect the Ca2+ signal and thus the amplitude and time course of the release probability. Since many aspects of the signalling cascade were first conceived with reference to the squid giant presynaptic terminal, we include comparisons with the squid model and revisit some of its implications. Whilst the characteristics of buffered Ca2+ diffusion presented here are based on the calyx of Held, we demonstrate the circumstances under which they may be valid for other nerve terminals at mammalian CNS synapses.
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Ca2+ entering the active zone via Ca2+ channels is buffered away quickly, leading to Ca2+-transients of less than 1 ms.
“Ca2+ entering the active zone via Ca2+ channels is buffered away quickly, leading to Ca2+-transients of less than 1 ms (Meinrenken et al., 2003).”
From The Presynaptic Active Zone (2012) · cites this paper as Meinrenken et al., 2003
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- Authors
- Meinrenken, C. J., Borst, J. G. G., & Sakmann, B.
- Affiliations
- Max Planck Institute for Medical Research (DE)
- Max Planck Society (DE)
- Venue
- The Journal of Physiology
- Publisher
- Wiley
- Published
- 2003-01-31
- Volume
- 547
- Issue
- 3
- Pages
- 665-689
- ISSN
- 0022-3751 (ISSN-L)
- PMC
- PMC2342725
- OpenAlex
- W2085537082
- Cited by
- 183
- References
- 0
- Citations by year
- 2025: 5 · 2023: 2 · 2022: 3 · 2021: 2 · 2020: 2 · 2019: 7 · 2018: 7 · 2017: 6 · 2016: 7 · 2015: 5 · 2014: 8 · 2013: 5 · 2012: 12
- FWCI
- 6.05
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- The Journal of Physiology (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- EUR Research Repository (Erasmus University Rotterdam) (publishedVersion)
- EUR Research Repository (Erasmus University Rotterdam) (submittedVersion)
- Max Planck Institute for Plasma Physics (submittedVersion)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Cellular transport and secretion
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Ion channel regulation and function
- Keywords
- calyx of Held, calcium buffering, calcium diffusion, voltage-gated calcium channels, release probability, squid giant axon, presynaptic terminals, synaptic transmission
- MeSH terms
- Animals, Synaptic Transmission, Neurons, Presynaptic Terminals, Calcium Signaling, Rats
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