Abstract
Short-term synaptic plasticity is a defining feature of neuronal activity, but the underlying molecular mechanisms are poorly understood. Depression of synaptic activity might be due to limited vesicle availability, whereas facilitation is thought to result from elevated calcium levels. However, it is unclear whether the strength and direction (facilitation versus depression) of plasticity at a given synapse result from preexisting synaptic strength or whether they are regulated by separate mechanisms. Here we show, in rat hippocampal cell cultures, that increases in the calcium binding protein neuronal calcium sensor-1 (NCS-1) can switch paired-pulse depression to facilitation without altering basal synaptic transmission or initial neurotransmitter release probability. Facilitation persisted during high-frequency trains of stimulation, indicating that NCS-1 can recruit 'dormant' vesicles. Our results suggest that NCS-1 acts as a calcium sensor for short-term plasticity by facilitating neurotransmitter output independent of initial release. We conclude that separate mechanisms are responsible for determining basal synaptic strength and short-term plasticity.
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References
Tsodyks, M.V. & Markram, H. The neural code between neocortical pyramidal neurons depends on neurotransmitter release probability. Proc. Natl. Acad. Sci. USA 94, 719–723 (1997).
Buonomano, D.V. Decoding temporal information: a model based on short-term synaptic plasticity. J. Neurosci. 20, 1129–1141 (2000).
Marder, E. From biophysics to models of network function. Annu. Rev. Neurosci. 21, 25–45 (1998).
Atwood, H.L. & Karunanithi, S. Diversification of synaptic strength: presynaptic elements. Nat. Rev. Neurosci. 3, 497–516 (2002).
Stevens, C.F. & Tsujimoto, T. Estimates for the pool size of releasable quanta at a single central synapse and for the time required to refill the pool. Proc. Natl. Acad. Sci. USA 92, 846–849 (1995).
Rosenmund, C. & Stevens, C.F. Definition of the readily releasable pool of vesicles at hippocampal synapses. Neuron 16, 1197–1207 (1996).
Waldeck, R.F., Pereda, A. & Faber, D.S. Properties and plasticity of paired-pulse depression at a central synapse. J. Neurosci. 20, 5312–5320 (2000).
Zucker, R.S. Calcium- and activity-dependent synaptic plasticity. Curr. Opin. Neurobiol. 9, 305–313 (1999).
Katz, B. & Miledi, R. The role of calcium in neuromuscular facilitation. J. Physiol. (Lond.) 195, 481–492 (1968).
Felmy, F., Neher, E. & Schneggenburger, R. Probing the Intracellular Calcium Sensitivity of Transmitter Release during Synaptic Facilitation. Neuron 37, 801–811 (2003).
Rozov, A., Burnashev, N., Sakmann, B. & Neher, E. Transmitter release modulation by intracellular Ca2+ buffers in facilitating and depressing nerve terminals of pyramidal cells in layer 2/3 of the rat neocortex indicates a target cell-specific difference in presynaptic calcium dynamics. J. Physiol. 531, 807–826 (2001).
Blatow, M., Caputi, A., Burnashev, N., Monyer, H. & Rozov, A. Ca2+ buffer saturation underlies paired pulse facilitation in calbindin-d28k-containing terminals. Neuron 38, 79–88 (2003).
Atluri, P.P. & Regehr, W.G. Determinants of the time course of facilitation at the granule cell to Purkinje cell synapse. J. Neurosci. 16, 5661–5671 (1996).
Zucker, R.S. & Regehr, W.G. Short-term synaptic plasticity. Annu. Rev. Physiol. 64, 355–405 (2002).
Pongs, O. et al. Frequenin: a novel calcium-binding protein that modulates synaptic efficacy in the Drosophila nervous system. Neuron 11, 15–28 (1993).
Burgoyne, R.D. & Weiss, J.L. The neuronal calcium sensor family of Ca2+-binding proteins. Biochem. J. 353, 1–12 (2001).
Olafsson, P., Wang, T. & Lu, B. Molecular cloning and functional characterization of the Xenopus Ca2+-binding protein frequenin. Proc. Natl. Acad. Sci. USA 92, 8001–8005 (1995).
Tsujimoto, T., Jeromin, A., Saitoh, N., Roder, J.C. & Takahashi, T. Neuronal calcium sensor 1 and activity-dependent facilitation of P/Q-type calcium currents at presynaptic nerve terminals. Science 295, 2276–2279 (2002).
Tong, G. & Jahr, C.E. Multivesicular release from excitatory synapses of cultured hippocampal neurons. Neuron 12, 51–59 (1994).
Wilcox, K.S. & Dichter, M.A. Paired pulse depression in cultured hippocampal neurons is due to a presynaptic mechanism independent of GABAB autoreceptor activation. J. Neurosci. 14, 1775–1788 (1994).
Debanne, D., Geahwiler, B.H. & Thompson, S.M. Long-term synaptic plasticity between pairs of individual CA3 pyramidal cells in rat hippocampal slice cultures. J. Physiol. (Lond.) 507, 237–247 (1998).
Weiss, J.L., Archer, D.A. & Burgoyne, R.D. Neuronal Ca2+ sensor-1/frequenin functions in an autocrine pathway regulating Ca2+ channels in bovine adrenal chromaffin cells. J. Biol. Chem. 275, 40082–40087 (2000).
Rajebhosale, M., Greenwood, S., Vidugiriene, J., Jeromin, A. & Hilfiker, S. Phosphatidylinositol 4-OH kinase is a downstream target of neuronal calcium sensor-1 in enhancing exocytosis in neuroendocrine cells. J. Biol. Chem. 278, 6075–6084 (2003).
McFerran, B.W., Weiss, J.L. & Burgoyne, R.D. Neuronal Ca2+ sensor 1. Characterization of the myristoylated protein, its cellular effects in permeabilized adrenal chromaffin cells, Ca2+-independent membrane association, and interaction with binding proteins, suggesting a role in rapid Ca2+ signal transduction. J. Biol. Chem. 274, 30258–30265 (1999).
Jinno, S., Jeromin, A., Roder, J. & Kosaka, T. Immunocytochemical localization of neuronal calcium sensor-1 in the hippocampus and cerebellum of the mouse, with special reference to presynaptic terminals. Neuroscience 113, 449–461 (2002).
Cummings, D.D., Wilcox, K.S. & Dichter, M.A. Calcium-dependent paired-pulse facilitation of miniature EPSC frequency accompanies depression of EPSCs at hippocampal synapses in culture. J. Neurosci. 16, 5312–5323 (1996).
Weiss, J.L. & Burgoyne, R.D. Voltage-independent inhibition of P/Q-type Ca2+ channels in adrenal chromaffin cells via a neuronal Ca2+ sensor-1-dependent pathway involves Src family tyrosine kinase. J. Biol. Chem. 276, 44804–44811 (2001).
Wheeler, D.B., Randall, A. & Tsien, R.W. Roles of N-type and Q-type Ca2+ channels in supporting hippocampal synaptic transmission. Science 264, 107–111 (1994).
Huettner, J.E. & Bean, B.P. Block of N-methyl-D-aspartate-activated current by the anticonvulsant MK-801: selective binding to open channels. Proc. Natl. Acad. Sci. USA 85, 1307–1311 (1988).
Hessler, N.A., Shirke, A.M. & Malinow, R. The probability of transmitter release at a mammalian central synapse. Nature 366, 569–572 (1993).
Rosenmund, C., Clements, J.D. & Westbrook, G.L. Nonuniform probability of glutamate release at a hippocampal synapse. Science 262, 754–757 (1993).
McFerran, B.W., Graham, M.E. & Burgoyne, R.D. Neuronal Ca2+ sensor 1, the mammalian homologue of frequenin, is expressed in chromaffin and PC12 cells and regulates neurosecretion from dense-core granules. J. Biol. Chem. 273, 22768–22772 (1998).
Koizumi, S. et al. Mechanisms underlying the neuronal calcium sensor-1-evoked enhancement of exocytosis in PC12 cells. J. Biol. Chem. 277, 30315–30324 (2002).
Rivosecchi, R., Pongs, O., Theil, T. & Mallart, A. Implication of frequenin in the facilitation of transmitter release in Drosophila. J. Physiol. 474, 223–232 (1994).
Cox, J.A. et al. Cation binding and conformational changes in VILIP and NCS-1, two neuron-specific calcium-binding proteins. J. Biol. Chem. 269, 32807–32813 (1994).
Zucker, R.S. Increased Ca2+ buffering enhances Ca2+-dependent process. J. Physiol. 531, 583 (2001).
Vyshedskiy, A., Allana, T. & Lin, J.W. Analysis of presynaptic Ca2+ influx and transmitter release kinetics during facilitation at the inhibitor of the crayfish neuromuscular junction. J. Neurosci. 20, 6326–6332 (2000).
Salin, P.A., Scanziani, M., Malenka, R.C. & Nicoll, R.A. Distinct short-term plasticity at two excitatory synapses in the hippocampus. Proc. Natl. Acad. Sci. USA 93, 13304–13309 (1996).
Genin, A. et al. Regulated expression of the neuronal calcium sensor-1 gene during long-term potentiation in the dentate gyrus in vivo. Neuroscience 106, 571–577 (2001).
Koh, P.O. et al. Up-regulation of neuronal calcium sensor-1 (NCS-1) in the prefrontal cortex of schizophrenic and bipolar patients. Proc. Natl. Acad. Sci. USA 100, 313–317 (2003).
Ryan, T.A. et al. The kinetics of synaptic vesicle recycling measured at single presynaptic boutons. Neuron 11, 713–724 (1993).
Threadgill, R., Bobb, K. & Ghosh, A. Regulation of dendritic growth and remodeling by Rho, Rac and Cdc42. Neuron 19, 625–634 (1997).
Acknowledgements
We thank B. Hargrove for technical assistance and all members of the Schweizer lab. We are also grateful to D. Buonomano, A. Dempsey, J.L. Feldman, M. Klein, N.A. Lambert, K.C. Martin, T.S. Otis, T.J. O'Dell, S.L. Smith and S.A. White for valuable and encouraging discussions, and H.T. Blair for help with statistics. This work was supported by grants from the Whitehall Foundation and the National Institutes of Health (NS41317) to F.E.S.
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Sippy, T., Cruz-Martín, A., Jeromin, A. et al. Acute changes in short-term plasticity at synapses with elevated levels of neuronal calcium sensor-1. Nat Neurosci 6, 1031–1038 (2003). https://doi.org/10.1038/nn1117
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DOI: https://doi.org/10.1038/nn1117