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Facilitation versus depression in cultured hippocampal neurons determined by targeting of Ca(2+) channel Ca(v)β(4) versus Ca(v)β(2) subunits to synaptic terminals

Ca(2+) channel β subunits determine the transport and physiological properties of high voltage–activated Ca(2+) channel complexes. Our analysis of the distribution of the Ca(v)β subunit family members in hippocampal neurons correlates their synaptic distribution with their involvement in transmitter...

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Detalles Bibliográficos
Autores principales: Xie, Mian, Li, Xiang, Han, Jing, Vogt, Daniel L., Wittemann, Silke, Mark, Melanie D., Herlitze, Stefan
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2064847/
https://www.ncbi.nlm.nih.gov/pubmed/17664337
http://dx.doi.org/10.1083/jcb.200702072
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author Xie, Mian
Li, Xiang
Han, Jing
Vogt, Daniel L.
Wittemann, Silke
Mark, Melanie D.
Herlitze, Stefan
author_facet Xie, Mian
Li, Xiang
Han, Jing
Vogt, Daniel L.
Wittemann, Silke
Mark, Melanie D.
Herlitze, Stefan
author_sort Xie, Mian
collection PubMed
description Ca(2+) channel β subunits determine the transport and physiological properties of high voltage–activated Ca(2+) channel complexes. Our analysis of the distribution of the Ca(v)β subunit family members in hippocampal neurons correlates their synaptic distribution with their involvement in transmitter release. We find that exogenously expressed Ca(v)β(4b) and Ca(v)β(2a) subunits distribute in clusters and localize to synapses, whereas Ca(v)β(1b) and Ca(v)β(3) are homogenously distributed. According to their localization, Ca(v)β(2a) and Ca(v)β(4b) subunits modulate the synaptic plasticity of autaptic hippocampal neurons (i.e., Ca(v)β(2a) induces depression, whereas Ca(v)β(4b) induces paired-pulse facilitation [PPF] followed by synaptic depression during longer stimuli trains). The induction of PPF by Ca(v)β(4b) correlates with a reduction in the release probability and cooperativity of the transmitter release. These results suggest that Ca(v)β subunits determine the gating properties of the presynaptic Ca(2+) channels within the presynaptic terminal in a subunit-specific manner and may be involved in organization of the Ca(2+) channel relative to the release machinery.
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spelling pubmed-20648472008-01-30 Facilitation versus depression in cultured hippocampal neurons determined by targeting of Ca(2+) channel Ca(v)β(4) versus Ca(v)β(2) subunits to synaptic terminals Xie, Mian Li, Xiang Han, Jing Vogt, Daniel L. Wittemann, Silke Mark, Melanie D. Herlitze, Stefan J Cell Biol Research Articles Ca(2+) channel β subunits determine the transport and physiological properties of high voltage–activated Ca(2+) channel complexes. Our analysis of the distribution of the Ca(v)β subunit family members in hippocampal neurons correlates their synaptic distribution with their involvement in transmitter release. We find that exogenously expressed Ca(v)β(4b) and Ca(v)β(2a) subunits distribute in clusters and localize to synapses, whereas Ca(v)β(1b) and Ca(v)β(3) are homogenously distributed. According to their localization, Ca(v)β(2a) and Ca(v)β(4b) subunits modulate the synaptic plasticity of autaptic hippocampal neurons (i.e., Ca(v)β(2a) induces depression, whereas Ca(v)β(4b) induces paired-pulse facilitation [PPF] followed by synaptic depression during longer stimuli trains). The induction of PPF by Ca(v)β(4b) correlates with a reduction in the release probability and cooperativity of the transmitter release. These results suggest that Ca(v)β subunits determine the gating properties of the presynaptic Ca(2+) channels within the presynaptic terminal in a subunit-specific manner and may be involved in organization of the Ca(2+) channel relative to the release machinery. The Rockefeller University Press 2007-07-30 /pmc/articles/PMC2064847/ /pubmed/17664337 http://dx.doi.org/10.1083/jcb.200702072 Text en Copyright © 2007, The Rockefeller University Press This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Research Articles
Xie, Mian
Li, Xiang
Han, Jing
Vogt, Daniel L.
Wittemann, Silke
Mark, Melanie D.
Herlitze, Stefan
Facilitation versus depression in cultured hippocampal neurons determined by targeting of Ca(2+) channel Ca(v)β(4) versus Ca(v)β(2) subunits to synaptic terminals
title Facilitation versus depression in cultured hippocampal neurons determined by targeting of Ca(2+) channel Ca(v)β(4) versus Ca(v)β(2) subunits to synaptic terminals
title_full Facilitation versus depression in cultured hippocampal neurons determined by targeting of Ca(2+) channel Ca(v)β(4) versus Ca(v)β(2) subunits to synaptic terminals
title_fullStr Facilitation versus depression in cultured hippocampal neurons determined by targeting of Ca(2+) channel Ca(v)β(4) versus Ca(v)β(2) subunits to synaptic terminals
title_full_unstemmed Facilitation versus depression in cultured hippocampal neurons determined by targeting of Ca(2+) channel Ca(v)β(4) versus Ca(v)β(2) subunits to synaptic terminals
title_short Facilitation versus depression in cultured hippocampal neurons determined by targeting of Ca(2+) channel Ca(v)β(4) versus Ca(v)β(2) subunits to synaptic terminals
title_sort facilitation versus depression in cultured hippocampal neurons determined by targeting of ca(2+) channel ca(v)β(4) versus ca(v)β(2) subunits to synaptic terminals
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2064847/
https://www.ncbi.nlm.nih.gov/pubmed/17664337
http://dx.doi.org/10.1083/jcb.200702072
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