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Organelle-Specific Sensors for Monitoring Ca(2+) Dynamics in Neurons
Calcium (Ca(2+)) plays innumerable critical functions in neurons ranging from regulation of neurotransmitter release and synaptic plasticity to activity-dependent transcription. Therefore, more than any other cell types, neurons are critically dependent on spatially and temporally controlled Ca(2+)...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2016
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5025517/ https://www.ncbi.nlm.nih.gov/pubmed/27695411 http://dx.doi.org/10.3389/fnsyn.2016.00029 |
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author | Kwon, Seok-Kyu Hirabayashi, Yusuke Polleux, Franck |
author_facet | Kwon, Seok-Kyu Hirabayashi, Yusuke Polleux, Franck |
author_sort | Kwon, Seok-Kyu |
collection | PubMed |
description | Calcium (Ca(2+)) plays innumerable critical functions in neurons ranging from regulation of neurotransmitter release and synaptic plasticity to activity-dependent transcription. Therefore, more than any other cell types, neurons are critically dependent on spatially and temporally controlled Ca(2+) dynamics. This is achieved through an exquisite level of compartmentalization of Ca(2+) storage and release from various organelles. The function of these organelles in the regulation of Ca(2+) dynamics has been studied for decades using electrophysiological and optical methods combined with pharmacological and genetic alterations. Mitochondria and the endoplasmic reticulum (ER) are among the organelles playing the most critical roles in Ca(2+) dynamics in neurons. At presynaptic boutons, Ca(2+) triggers neurotransmitter release and synaptic plasticity, and postsynaptically, Ca(2+) mobilization mediates long-term synaptic plasticity. To explore Ca(2+) dynamics in live cells and intact animals, various synthetic and genetically encoded fluorescent Ca(2+) sensors were developed, and recently, many groups actively increased the sensitivity and diversity of genetically encoded Ca(2+) indicators (GECIs). Following conjugation with various signal peptides, these improved GECIs can be targeted to specific subcellular compartments, allowing monitoring of organelle-specific Ca(2+) dynamics. Here, we review recent findings unraveling novel roles for mitochondria- and ER-dependent Ca(2+) dynamics in neurons and at synapses. |
format | Online Article Text |
id | pubmed-5025517 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-50255172016-09-30 Organelle-Specific Sensors for Monitoring Ca(2+) Dynamics in Neurons Kwon, Seok-Kyu Hirabayashi, Yusuke Polleux, Franck Front Synaptic Neurosci Neuroscience Calcium (Ca(2+)) plays innumerable critical functions in neurons ranging from regulation of neurotransmitter release and synaptic plasticity to activity-dependent transcription. Therefore, more than any other cell types, neurons are critically dependent on spatially and temporally controlled Ca(2+) dynamics. This is achieved through an exquisite level of compartmentalization of Ca(2+) storage and release from various organelles. The function of these organelles in the regulation of Ca(2+) dynamics has been studied for decades using electrophysiological and optical methods combined with pharmacological and genetic alterations. Mitochondria and the endoplasmic reticulum (ER) are among the organelles playing the most critical roles in Ca(2+) dynamics in neurons. At presynaptic boutons, Ca(2+) triggers neurotransmitter release and synaptic plasticity, and postsynaptically, Ca(2+) mobilization mediates long-term synaptic plasticity. To explore Ca(2+) dynamics in live cells and intact animals, various synthetic and genetically encoded fluorescent Ca(2+) sensors were developed, and recently, many groups actively increased the sensitivity and diversity of genetically encoded Ca(2+) indicators (GECIs). Following conjugation with various signal peptides, these improved GECIs can be targeted to specific subcellular compartments, allowing monitoring of organelle-specific Ca(2+) dynamics. Here, we review recent findings unraveling novel roles for mitochondria- and ER-dependent Ca(2+) dynamics in neurons and at synapses. Frontiers Media S.A. 2016-09-16 /pmc/articles/PMC5025517/ /pubmed/27695411 http://dx.doi.org/10.3389/fnsyn.2016.00029 Text en Copyright © 2016 Kwon, Hirabayashi and Polleux. 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 Kwon, Seok-Kyu Hirabayashi, Yusuke Polleux, Franck Organelle-Specific Sensors for Monitoring Ca(2+) Dynamics in Neurons |
title | Organelle-Specific Sensors for Monitoring Ca(2+) Dynamics in Neurons |
title_full | Organelle-Specific Sensors for Monitoring Ca(2+) Dynamics in Neurons |
title_fullStr | Organelle-Specific Sensors for Monitoring Ca(2+) Dynamics in Neurons |
title_full_unstemmed | Organelle-Specific Sensors for Monitoring Ca(2+) Dynamics in Neurons |
title_short | Organelle-Specific Sensors for Monitoring Ca(2+) Dynamics in Neurons |
title_sort | organelle-specific sensors for monitoring ca(2+) dynamics in neurons |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5025517/ https://www.ncbi.nlm.nih.gov/pubmed/27695411 http://dx.doi.org/10.3389/fnsyn.2016.00029 |
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