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Visualizing synaptic dopamine efflux with a 2D composite nanofilm
Chemical neurotransmission constitutes one of the fundamental modalities of communication between neurons. Monitoring release of these chemicals has traditionally been difficult to carry out at spatial and temporal scales relevant to neuron function. To understand chemical neurotransmission more ful...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9363124/ https://www.ncbi.nlm.nih.gov/pubmed/35786443 http://dx.doi.org/10.7554/eLife.78773 |
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author | Bulumulla, Chandima Krasley, Andrew T Cristofori-Armstrong, Ben Valinsky, William C Walpita, Deepika Ackerman, David Clapham, David E Beyene, Abraham G |
author_facet | Bulumulla, Chandima Krasley, Andrew T Cristofori-Armstrong, Ben Valinsky, William C Walpita, Deepika Ackerman, David Clapham, David E Beyene, Abraham G |
author_sort | Bulumulla, Chandima |
collection | PubMed |
description | Chemical neurotransmission constitutes one of the fundamental modalities of communication between neurons. Monitoring release of these chemicals has traditionally been difficult to carry out at spatial and temporal scales relevant to neuron function. To understand chemical neurotransmission more fully, we need to improve the spatial and temporal resolutions of measurements for neurotransmitter release. To address this, we engineered a chemi-sensitive, two-dimensional composite nanofilm that facilitates visualization of the release and diffusion of the neurochemical dopamine with synaptic resolution, quantal sensitivity, and simultaneously from hundreds of release sites. Using this technology, we were able to monitor the spatiotemporal dynamics of dopamine release in dendritic processes, a poorly understood phenomenon. We found that dopamine release is broadcast from a subset of dendritic processes as hotspots that have a mean spatial spread of ≈ 3.2 µm (full width at half maximum [FWHM]) and are observed with a mean spatial frequency of one hotspot per ≈ 7.5 µm of dendritic length. Major dendrites of dopamine neurons and fine dendritic processes, as well as dendritic arbors and dendrites with no apparent varicose morphology participated in dopamine release. Remarkably, these release hotspots co-localized with Bassoon, suggesting that Bassoon may contribute to organizing active zones in dendrites, similar to its role in axon terminals. |
format | Online Article Text |
id | pubmed-9363124 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-93631242022-08-10 Visualizing synaptic dopamine efflux with a 2D composite nanofilm Bulumulla, Chandima Krasley, Andrew T Cristofori-Armstrong, Ben Valinsky, William C Walpita, Deepika Ackerman, David Clapham, David E Beyene, Abraham G eLife Neuroscience Chemical neurotransmission constitutes one of the fundamental modalities of communication between neurons. Monitoring release of these chemicals has traditionally been difficult to carry out at spatial and temporal scales relevant to neuron function. To understand chemical neurotransmission more fully, we need to improve the spatial and temporal resolutions of measurements for neurotransmitter release. To address this, we engineered a chemi-sensitive, two-dimensional composite nanofilm that facilitates visualization of the release and diffusion of the neurochemical dopamine with synaptic resolution, quantal sensitivity, and simultaneously from hundreds of release sites. Using this technology, we were able to monitor the spatiotemporal dynamics of dopamine release in dendritic processes, a poorly understood phenomenon. We found that dopamine release is broadcast from a subset of dendritic processes as hotspots that have a mean spatial spread of ≈ 3.2 µm (full width at half maximum [FWHM]) and are observed with a mean spatial frequency of one hotspot per ≈ 7.5 µm of dendritic length. Major dendrites of dopamine neurons and fine dendritic processes, as well as dendritic arbors and dendrites with no apparent varicose morphology participated in dopamine release. Remarkably, these release hotspots co-localized with Bassoon, suggesting that Bassoon may contribute to organizing active zones in dendrites, similar to its role in axon terminals. eLife Sciences Publications, Ltd 2022-07-04 /pmc/articles/PMC9363124/ /pubmed/35786443 http://dx.doi.org/10.7554/eLife.78773 Text en © 2022, Bulumulla et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Neuroscience Bulumulla, Chandima Krasley, Andrew T Cristofori-Armstrong, Ben Valinsky, William C Walpita, Deepika Ackerman, David Clapham, David E Beyene, Abraham G Visualizing synaptic dopamine efflux with a 2D composite nanofilm |
title | Visualizing synaptic dopamine efflux with a 2D composite nanofilm |
title_full | Visualizing synaptic dopamine efflux with a 2D composite nanofilm |
title_fullStr | Visualizing synaptic dopamine efflux with a 2D composite nanofilm |
title_full_unstemmed | Visualizing synaptic dopamine efflux with a 2D composite nanofilm |
title_short | Visualizing synaptic dopamine efflux with a 2D composite nanofilm |
title_sort | visualizing synaptic dopamine efflux with a 2d composite nanofilm |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9363124/ https://www.ncbi.nlm.nih.gov/pubmed/35786443 http://dx.doi.org/10.7554/eLife.78773 |
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