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Patch clamp recording from bipolar cells in the wholemount mouse retina

Bipolar cells are the second-order neurons in the retina that are less accessible for investigating their synaptic responses. Here, we present a protocol to conduct patch clamp recordings from bipolar cells in the wholemount retina from Ai32 mutant mice. We detail whole-cell patch-clamp recording fr...

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Detalles Bibliográficos
Autores principales: Bohl, Jeremy M., Shehu, Angela, Hellmer, Chase B., Ichinose, Tomomi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9234155/
https://www.ncbi.nlm.nih.gov/pubmed/35769922
http://dx.doi.org/10.1016/j.xpro.2022.101482
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author Bohl, Jeremy M.
Shehu, Angela
Hellmer, Chase B.
Ichinose, Tomomi
author_facet Bohl, Jeremy M.
Shehu, Angela
Hellmer, Chase B.
Ichinose, Tomomi
author_sort Bohl, Jeremy M.
collection PubMed
description Bipolar cells are the second-order neurons in the retina that are less accessible for investigating their synaptic responses. Here, we present a protocol to conduct patch clamp recordings from bipolar cells in the wholemount retina from Ai32 mutant mice. We detail whole-cell patch-clamp recording from bipolar cells to examine their light-evoked responses to optogenetic stimulation, followed by imaging terminals of recorded cells to determine bipolar cell type. We describe light stimulus information to activate channelrhodopsin-2 (ChR2). For complete details on the use and execution of this protocol, please refer to Hellmer et al. (2021).
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spelling pubmed-92341552022-06-28 Patch clamp recording from bipolar cells in the wholemount mouse retina Bohl, Jeremy M. Shehu, Angela Hellmer, Chase B. Ichinose, Tomomi STAR Protoc Protocol Bipolar cells are the second-order neurons in the retina that are less accessible for investigating their synaptic responses. Here, we present a protocol to conduct patch clamp recordings from bipolar cells in the wholemount retina from Ai32 mutant mice. We detail whole-cell patch-clamp recording from bipolar cells to examine their light-evoked responses to optogenetic stimulation, followed by imaging terminals of recorded cells to determine bipolar cell type. We describe light stimulus information to activate channelrhodopsin-2 (ChR2). For complete details on the use and execution of this protocol, please refer to Hellmer et al. (2021). Elsevier 2022-06-17 /pmc/articles/PMC9234155/ /pubmed/35769922 http://dx.doi.org/10.1016/j.xpro.2022.101482 Text en © 2022 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Protocol
Bohl, Jeremy M.
Shehu, Angela
Hellmer, Chase B.
Ichinose, Tomomi
Patch clamp recording from bipolar cells in the wholemount mouse retina
title Patch clamp recording from bipolar cells in the wholemount mouse retina
title_full Patch clamp recording from bipolar cells in the wholemount mouse retina
title_fullStr Patch clamp recording from bipolar cells in the wholemount mouse retina
title_full_unstemmed Patch clamp recording from bipolar cells in the wholemount mouse retina
title_short Patch clamp recording from bipolar cells in the wholemount mouse retina
title_sort patch clamp recording from bipolar cells in the wholemount mouse retina
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9234155/
https://www.ncbi.nlm.nih.gov/pubmed/35769922
http://dx.doi.org/10.1016/j.xpro.2022.101482
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