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Mitochondrial support of persistent presynaptic vesicle mobilization with age-dependent synaptic growth after LTP
Mitochondria support synaptic transmission through production of ATP, sequestration of calcium, synthesis of glutamate, and other vital functions. Surprisingly, less than 50% of hippocampal CA1 presynaptic boutons contain mitochondria, raising the question of whether synapses without mitochondria ca...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5235352/ https://www.ncbi.nlm.nih.gov/pubmed/27991850 http://dx.doi.org/10.7554/eLife.15275 |
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author | Smith, Heather L Bourne, Jennifer N Cao, Guan Chirillo, Michael A Ostroff, Linnaea E Watson, Deborah J Harris, Kristen M |
author_facet | Smith, Heather L Bourne, Jennifer N Cao, Guan Chirillo, Michael A Ostroff, Linnaea E Watson, Deborah J Harris, Kristen M |
author_sort | Smith, Heather L |
collection | PubMed |
description | Mitochondria support synaptic transmission through production of ATP, sequestration of calcium, synthesis of glutamate, and other vital functions. Surprisingly, less than 50% of hippocampal CA1 presynaptic boutons contain mitochondria, raising the question of whether synapses without mitochondria can sustain changes in efficacy. To address this question, we analyzed synapses from postnatal day 15 (P15) and adult rat hippocampus that had undergone theta-burst stimulation to produce long-term potentiation (TBS-LTP) and compared them to control or no stimulation. At 30 and 120 min after TBS-LTP, vesicles were decreased only in presynaptic boutons that contained mitochondria at P15, and vesicle decrement was greatest in adult boutons containing mitochondria. Presynaptic mitochondrial cristae were widened, suggesting a sustained energy demand. Thus, mitochondrial proximity reflected enhanced vesicle mobilization well after potentiation reached asymptote, in parallel with the apparently silent addition of new dendritic spines at P15 or the silent enlargement of synapses in adults. DOI: http://dx.doi.org/10.7554/eLife.15275.001 |
format | Online Article Text |
id | pubmed-5235352 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-52353522017-01-17 Mitochondrial support of persistent presynaptic vesicle mobilization with age-dependent synaptic growth after LTP Smith, Heather L Bourne, Jennifer N Cao, Guan Chirillo, Michael A Ostroff, Linnaea E Watson, Deborah J Harris, Kristen M eLife Cell Biology Mitochondria support synaptic transmission through production of ATP, sequestration of calcium, synthesis of glutamate, and other vital functions. Surprisingly, less than 50% of hippocampal CA1 presynaptic boutons contain mitochondria, raising the question of whether synapses without mitochondria can sustain changes in efficacy. To address this question, we analyzed synapses from postnatal day 15 (P15) and adult rat hippocampus that had undergone theta-burst stimulation to produce long-term potentiation (TBS-LTP) and compared them to control or no stimulation. At 30 and 120 min after TBS-LTP, vesicles were decreased only in presynaptic boutons that contained mitochondria at P15, and vesicle decrement was greatest in adult boutons containing mitochondria. Presynaptic mitochondrial cristae were widened, suggesting a sustained energy demand. Thus, mitochondrial proximity reflected enhanced vesicle mobilization well after potentiation reached asymptote, in parallel with the apparently silent addition of new dendritic spines at P15 or the silent enlargement of synapses in adults. DOI: http://dx.doi.org/10.7554/eLife.15275.001 eLife Sciences Publications, Ltd 2016-12-19 /pmc/articles/PMC5235352/ /pubmed/27991850 http://dx.doi.org/10.7554/eLife.15275 Text en © 2016, Smith et al http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Cell Biology Smith, Heather L Bourne, Jennifer N Cao, Guan Chirillo, Michael A Ostroff, Linnaea E Watson, Deborah J Harris, Kristen M Mitochondrial support of persistent presynaptic vesicle mobilization with age-dependent synaptic growth after LTP |
title | Mitochondrial support of persistent presynaptic vesicle mobilization with age-dependent synaptic growth after LTP |
title_full | Mitochondrial support of persistent presynaptic vesicle mobilization with age-dependent synaptic growth after LTP |
title_fullStr | Mitochondrial support of persistent presynaptic vesicle mobilization with age-dependent synaptic growth after LTP |
title_full_unstemmed | Mitochondrial support of persistent presynaptic vesicle mobilization with age-dependent synaptic growth after LTP |
title_short | Mitochondrial support of persistent presynaptic vesicle mobilization with age-dependent synaptic growth after LTP |
title_sort | mitochondrial support of persistent presynaptic vesicle mobilization with age-dependent synaptic growth after ltp |
topic | Cell Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5235352/ https://www.ncbi.nlm.nih.gov/pubmed/27991850 http://dx.doi.org/10.7554/eLife.15275 |
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