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The role of cAMP in synaptic homeostasis in response to environmental temperature challenges and hyperexcitability mutations
Homeostasis is the ability of physiological systems to regain functional balance following environment or experimental insults and synaptic homeostasis has been demonstrated in various species following genetic or pharmacological disruptions. Among environmental challenges, homeostatic responses to...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2015
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4313691/ https://www.ncbi.nlm.nih.gov/pubmed/25698925 http://dx.doi.org/10.3389/fncel.2015.00010 |
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author | Ueda, Atsushi Wu, Chun-Fang |
author_facet | Ueda, Atsushi Wu, Chun-Fang |
author_sort | Ueda, Atsushi |
collection | PubMed |
description | Homeostasis is the ability of physiological systems to regain functional balance following environment or experimental insults and synaptic homeostasis has been demonstrated in various species following genetic or pharmacological disruptions. Among environmental challenges, homeostatic responses to temperature extremes are critical to animal survival under natural conditions. We previously reported that axon terminal arborization in Drosophila larval neuromuscular junctions (NMJs) is enhanced at elevated temperatures; however, the amplitude of excitatory junctional potentials (EJPs) remains unaltered despite the increase in synaptic bouton numbers. Here we determine the cellular basis of this homeostatic adjustment in larvae reared at high temperature (HT, 29°C). We found that synaptic current focally recorded from individual synaptic boutons was unaffected by rearing temperature (<15°C to >30°C). However, HT rearing decreased the quantal size (amplitude of spontaneous miniature EJPs, or mEJPs), which compensates for the increased number of synaptic releasing sites to retain a normal EJP size. The quantal size decrease is accounted for by a decrease in input resistance of the postsynaptic muscle fiber, indicating an increase in membrane area that matches the synaptic growth at HT. Interestingly, a mutation in rutabaga (rut) encoding adenylyl cyclase (AC) exhibited no obvious changes in quantal size or input resistance of postsynaptic muscle cells after HT rearing, suggesting an important role for rut AC in temperature-induced synaptic homeostasis in Drosophila. This extends our previous finding of rut-dependent synaptic homeostasis in hyperexcitable mutants, e.g., slowpoke (slo). In slo larvae, the lack of BK channel function is partially ameliorated by upregulation of presynaptic Shaker (Sh) IA current to limit excessive transmitter release in addition to postsynaptic glutamate receptor recomposition that reduces the quantal size. |
format | Online Article Text |
id | pubmed-4313691 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-43136912015-02-19 The role of cAMP in synaptic homeostasis in response to environmental temperature challenges and hyperexcitability mutations Ueda, Atsushi Wu, Chun-Fang Front Cell Neurosci Neuroscience Homeostasis is the ability of physiological systems to regain functional balance following environment or experimental insults and synaptic homeostasis has been demonstrated in various species following genetic or pharmacological disruptions. Among environmental challenges, homeostatic responses to temperature extremes are critical to animal survival under natural conditions. We previously reported that axon terminal arborization in Drosophila larval neuromuscular junctions (NMJs) is enhanced at elevated temperatures; however, the amplitude of excitatory junctional potentials (EJPs) remains unaltered despite the increase in synaptic bouton numbers. Here we determine the cellular basis of this homeostatic adjustment in larvae reared at high temperature (HT, 29°C). We found that synaptic current focally recorded from individual synaptic boutons was unaffected by rearing temperature (<15°C to >30°C). However, HT rearing decreased the quantal size (amplitude of spontaneous miniature EJPs, or mEJPs), which compensates for the increased number of synaptic releasing sites to retain a normal EJP size. The quantal size decrease is accounted for by a decrease in input resistance of the postsynaptic muscle fiber, indicating an increase in membrane area that matches the synaptic growth at HT. Interestingly, a mutation in rutabaga (rut) encoding adenylyl cyclase (AC) exhibited no obvious changes in quantal size or input resistance of postsynaptic muscle cells after HT rearing, suggesting an important role for rut AC in temperature-induced synaptic homeostasis in Drosophila. This extends our previous finding of rut-dependent synaptic homeostasis in hyperexcitable mutants, e.g., slowpoke (slo). In slo larvae, the lack of BK channel function is partially ameliorated by upregulation of presynaptic Shaker (Sh) IA current to limit excessive transmitter release in addition to postsynaptic glutamate receptor recomposition that reduces the quantal size. Frontiers Media S.A. 2015-02-02 /pmc/articles/PMC4313691/ /pubmed/25698925 http://dx.doi.org/10.3389/fncel.2015.00010 Text en Copyright © 2015 Ueda and Wu. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution and reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neuroscience Ueda, Atsushi Wu, Chun-Fang The role of cAMP in synaptic homeostasis in response to environmental temperature challenges and hyperexcitability mutations |
title | The role of cAMP in synaptic homeostasis in response to environmental temperature challenges and hyperexcitability mutations |
title_full | The role of cAMP in synaptic homeostasis in response to environmental temperature challenges and hyperexcitability mutations |
title_fullStr | The role of cAMP in synaptic homeostasis in response to environmental temperature challenges and hyperexcitability mutations |
title_full_unstemmed | The role of cAMP in synaptic homeostasis in response to environmental temperature challenges and hyperexcitability mutations |
title_short | The role of cAMP in synaptic homeostasis in response to environmental temperature challenges and hyperexcitability mutations |
title_sort | role of camp in synaptic homeostasis in response to environmental temperature challenges and hyperexcitability mutations |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4313691/ https://www.ncbi.nlm.nih.gov/pubmed/25698925 http://dx.doi.org/10.3389/fncel.2015.00010 |
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