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Multiplex imaging relates quantal glutamate release to presynaptic Ca(2+) homeostasis at multiple synapses in situ
Information processing by brain circuits depends on Ca(2+)-dependent, stochastic release of the excitatory neurotransmitter glutamate. Whilst optical glutamate sensors have enabled detection of synaptic discharges, understanding presynaptic machinery requires simultaneous readout of glutamate releas...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6441074/ https://www.ncbi.nlm.nih.gov/pubmed/30926781 http://dx.doi.org/10.1038/s41467-019-09216-8 |
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author | Jensen, Thomas P. Zheng, Kaiyu Cole, Nicholas Marvin, Jonathan S. Looger, Loren L. Rusakov, Dmitri A. |
author_facet | Jensen, Thomas P. Zheng, Kaiyu Cole, Nicholas Marvin, Jonathan S. Looger, Loren L. Rusakov, Dmitri A. |
author_sort | Jensen, Thomas P. |
collection | PubMed |
description | Information processing by brain circuits depends on Ca(2+)-dependent, stochastic release of the excitatory neurotransmitter glutamate. Whilst optical glutamate sensors have enabled detection of synaptic discharges, understanding presynaptic machinery requires simultaneous readout of glutamate release and nanomolar presynaptic Ca(2+) in situ. Here, we find that the fluorescence lifetime of the red-shifted Ca(2+) indicator Cal-590 is Ca(2+)-sensitive in the nanomolar range, and employ it in combination with green glutamate sensors to relate quantal neurotransmission to presynaptic Ca(2+) kinetics. Multiplexed imaging of individual and multiple synapses in identified axonal circuits reveals that glutamate release efficacy, but not its short-term plasticity, varies with time-dependent fluctuations in presynaptic resting Ca(2+) or spike-evoked Ca(2+) entry. Within individual presynaptic boutons, we find no nanoscopic co-localisation of evoked presynaptic Ca(2+) entry with the prevalent glutamate release site, suggesting loose coupling between the two. The approach enables a better understanding of release machinery at central synapses. |
format | Online Article Text |
id | pubmed-6441074 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-64410742019-04-01 Multiplex imaging relates quantal glutamate release to presynaptic Ca(2+) homeostasis at multiple synapses in situ Jensen, Thomas P. Zheng, Kaiyu Cole, Nicholas Marvin, Jonathan S. Looger, Loren L. Rusakov, Dmitri A. Nat Commun Article Information processing by brain circuits depends on Ca(2+)-dependent, stochastic release of the excitatory neurotransmitter glutamate. Whilst optical glutamate sensors have enabled detection of synaptic discharges, understanding presynaptic machinery requires simultaneous readout of glutamate release and nanomolar presynaptic Ca(2+) in situ. Here, we find that the fluorescence lifetime of the red-shifted Ca(2+) indicator Cal-590 is Ca(2+)-sensitive in the nanomolar range, and employ it in combination with green glutamate sensors to relate quantal neurotransmission to presynaptic Ca(2+) kinetics. Multiplexed imaging of individual and multiple synapses in identified axonal circuits reveals that glutamate release efficacy, but not its short-term plasticity, varies with time-dependent fluctuations in presynaptic resting Ca(2+) or spike-evoked Ca(2+) entry. Within individual presynaptic boutons, we find no nanoscopic co-localisation of evoked presynaptic Ca(2+) entry with the prevalent glutamate release site, suggesting loose coupling between the two. The approach enables a better understanding of release machinery at central synapses. Nature Publishing Group UK 2019-03-29 /pmc/articles/PMC6441074/ /pubmed/30926781 http://dx.doi.org/10.1038/s41467-019-09216-8 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Jensen, Thomas P. Zheng, Kaiyu Cole, Nicholas Marvin, Jonathan S. Looger, Loren L. Rusakov, Dmitri A. Multiplex imaging relates quantal glutamate release to presynaptic Ca(2+) homeostasis at multiple synapses in situ |
title | Multiplex imaging relates quantal glutamate release to presynaptic Ca(2+) homeostasis at multiple synapses in situ |
title_full | Multiplex imaging relates quantal glutamate release to presynaptic Ca(2+) homeostasis at multiple synapses in situ |
title_fullStr | Multiplex imaging relates quantal glutamate release to presynaptic Ca(2+) homeostasis at multiple synapses in situ |
title_full_unstemmed | Multiplex imaging relates quantal glutamate release to presynaptic Ca(2+) homeostasis at multiple synapses in situ |
title_short | Multiplex imaging relates quantal glutamate release to presynaptic Ca(2+) homeostasis at multiple synapses in situ |
title_sort | multiplex imaging relates quantal glutamate release to presynaptic ca(2+) homeostasis at multiple synapses in situ |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6441074/ https://www.ncbi.nlm.nih.gov/pubmed/30926781 http://dx.doi.org/10.1038/s41467-019-09216-8 |
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