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Differential modulation of short-term plasticity at hippocampal mossy fiber and Schaffer collateral synapses by mitochondrial Ca(2+)
Presynaptic mitochondrial Ca(2+) plays a critical role in the regulation of synaptic transmission and plasticity. The presynaptic bouton of the hippocampal mossy fiber (MF) is much larger in size than that of the Schaffer collateral (SC) synapse. Here we compare the structural and physiological char...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7553293/ https://www.ncbi.nlm.nih.gov/pubmed/33049001 http://dx.doi.org/10.1371/journal.pone.0240610 |
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author | Lee, Sang Hun Lutz, David Drexler, Dagmar Frotscher, Michael Shen, Jie |
author_facet | Lee, Sang Hun Lutz, David Drexler, Dagmar Frotscher, Michael Shen, Jie |
author_sort | Lee, Sang Hun |
collection | PubMed |
description | Presynaptic mitochondrial Ca(2+) plays a critical role in the regulation of synaptic transmission and plasticity. The presynaptic bouton of the hippocampal mossy fiber (MF) is much larger in size than that of the Schaffer collateral (SC) synapse. Here we compare the structural and physiological characteristics of MF and SC presynaptic boutons to reveal functional and mechanistic differences between these two synapses. Our quantitative ultrastructural analysis using electron microscopy show many more mitochondria in MF presynaptic bouton cross-section profiles compared to SC boutons. Consistent with these results, post-tetanic potentiation (PTP), a form of presynaptic short-term plasticity dependent on mitochondrial Ca(2+), is reduced by inhibition of mitochondrial Ca(2+) release at MF synapses but not at SC synapses. However, blockade of mitochondrial Ca(2+) release results in reduction of PTP at SC synapses by disynaptic MF stimulation. Furthermore, inhibition of mitochondrial Ca(2+) release selectively decreases frequency facilitation evoked by short trains of presynaptic stimulation at MF synapses, while having no effect at SC synapses. Moreover, depletion of ER Ca(2+) stores leads to reduction of PTP at MF synapses, but PTP is unaffected by ER Ca(2+) depletion at SC synapses. These findings show that MF and SC synapses differ in presynaptic mitochondrial content as well as mitochondrial Ca(2+) dependent synaptic plasticity, highlighting differential regulatory mechanisms of presynaptic plasticity at MF and SC synapses. |
format | Online Article Text |
id | pubmed-7553293 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-75532932020-10-21 Differential modulation of short-term plasticity at hippocampal mossy fiber and Schaffer collateral synapses by mitochondrial Ca(2+) Lee, Sang Hun Lutz, David Drexler, Dagmar Frotscher, Michael Shen, Jie PLoS One Research Article Presynaptic mitochondrial Ca(2+) plays a critical role in the regulation of synaptic transmission and plasticity. The presynaptic bouton of the hippocampal mossy fiber (MF) is much larger in size than that of the Schaffer collateral (SC) synapse. Here we compare the structural and physiological characteristics of MF and SC presynaptic boutons to reveal functional and mechanistic differences between these two synapses. Our quantitative ultrastructural analysis using electron microscopy show many more mitochondria in MF presynaptic bouton cross-section profiles compared to SC boutons. Consistent with these results, post-tetanic potentiation (PTP), a form of presynaptic short-term plasticity dependent on mitochondrial Ca(2+), is reduced by inhibition of mitochondrial Ca(2+) release at MF synapses but not at SC synapses. However, blockade of mitochondrial Ca(2+) release results in reduction of PTP at SC synapses by disynaptic MF stimulation. Furthermore, inhibition of mitochondrial Ca(2+) release selectively decreases frequency facilitation evoked by short trains of presynaptic stimulation at MF synapses, while having no effect at SC synapses. Moreover, depletion of ER Ca(2+) stores leads to reduction of PTP at MF synapses, but PTP is unaffected by ER Ca(2+) depletion at SC synapses. These findings show that MF and SC synapses differ in presynaptic mitochondrial content as well as mitochondrial Ca(2+) dependent synaptic plasticity, highlighting differential regulatory mechanisms of presynaptic plasticity at MF and SC synapses. Public Library of Science 2020-10-13 /pmc/articles/PMC7553293/ /pubmed/33049001 http://dx.doi.org/10.1371/journal.pone.0240610 Text en © 2020 Lee et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Lee, Sang Hun Lutz, David Drexler, Dagmar Frotscher, Michael Shen, Jie Differential modulation of short-term plasticity at hippocampal mossy fiber and Schaffer collateral synapses by mitochondrial Ca(2+) |
title | Differential modulation of short-term plasticity at hippocampal mossy fiber and Schaffer collateral synapses by mitochondrial Ca(2+) |
title_full | Differential modulation of short-term plasticity at hippocampal mossy fiber and Schaffer collateral synapses by mitochondrial Ca(2+) |
title_fullStr | Differential modulation of short-term plasticity at hippocampal mossy fiber and Schaffer collateral synapses by mitochondrial Ca(2+) |
title_full_unstemmed | Differential modulation of short-term plasticity at hippocampal mossy fiber and Schaffer collateral synapses by mitochondrial Ca(2+) |
title_short | Differential modulation of short-term plasticity at hippocampal mossy fiber and Schaffer collateral synapses by mitochondrial Ca(2+) |
title_sort | differential modulation of short-term plasticity at hippocampal mossy fiber and schaffer collateral synapses by mitochondrial ca(2+) |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7553293/ https://www.ncbi.nlm.nih.gov/pubmed/33049001 http://dx.doi.org/10.1371/journal.pone.0240610 |
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