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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...

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Autores principales: Bulumulla, Chandima, Krasley, Andrew T, Cristofori-Armstrong, Ben, Valinsky, William C, Walpita, Deepika, Ackerman, David, Clapham, David E, Beyene, Abraham G
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2022
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.
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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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