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Visualization of trans-interactions of a protocadherin-α between processes originating from single neurons

Clustered protocadherin (Pcdh), a cell adhesion protein, is involved in the self-recognition and non-self-discrimination of neurons by conferring diversity on the cell surface. Although the roles of Pcdh in neurons have been elucidated, it has been challenging to visualize its adhesion activity in n...

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Autores principales: Kanadome, Takashi, Hoshino, Natsumi, Nagai, Takeharu, Yagi, Takeshi, Matsuda, Tomoki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10392085/
https://www.ncbi.nlm.nih.gov/pubmed/37534169
http://dx.doi.org/10.1016/j.isci.2023.107238
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author Kanadome, Takashi
Hoshino, Natsumi
Nagai, Takeharu
Yagi, Takeshi
Matsuda, Tomoki
author_facet Kanadome, Takashi
Hoshino, Natsumi
Nagai, Takeharu
Yagi, Takeshi
Matsuda, Tomoki
author_sort Kanadome, Takashi
collection PubMed
description Clustered protocadherin (Pcdh), a cell adhesion protein, is involved in the self-recognition and non-self-discrimination of neurons by conferring diversity on the cell surface. Although the roles of Pcdh in neurons have been elucidated, it has been challenging to visualize its adhesion activity in neurons, which is a molecular function of Pcdh. Here, we present fluorescent indicators, named IPADs, which visualize the interaction of protocadherin-α4 isoform (α4). IPADs successfully visualize not only homophilic α4 trans-interactions, but also combinatorial homophilic interactions between cells. The reversible nature of IPADs overcomes a drawback of the split-GFP technique and allows for monitoring the dissociation of α4 trans-interactions. Specially designed IPADs for self-recognition are able to monitor the formation and disruption of α4 trans-interactions between processes originating from the same neurons. We expect that IPADs will be useful tools for obtaining spatiotemporal information on Pcdh interactions in neuronal self-recognition and non-self-discrimination processes.
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spelling pubmed-103920852023-08-02 Visualization of trans-interactions of a protocadherin-α between processes originating from single neurons Kanadome, Takashi Hoshino, Natsumi Nagai, Takeharu Yagi, Takeshi Matsuda, Tomoki iScience Article Clustered protocadherin (Pcdh), a cell adhesion protein, is involved in the self-recognition and non-self-discrimination of neurons by conferring diversity on the cell surface. Although the roles of Pcdh in neurons have been elucidated, it has been challenging to visualize its adhesion activity in neurons, which is a molecular function of Pcdh. Here, we present fluorescent indicators, named IPADs, which visualize the interaction of protocadherin-α4 isoform (α4). IPADs successfully visualize not only homophilic α4 trans-interactions, but also combinatorial homophilic interactions between cells. The reversible nature of IPADs overcomes a drawback of the split-GFP technique and allows for monitoring the dissociation of α4 trans-interactions. Specially designed IPADs for self-recognition are able to monitor the formation and disruption of α4 trans-interactions between processes originating from the same neurons. We expect that IPADs will be useful tools for obtaining spatiotemporal information on Pcdh interactions in neuronal self-recognition and non-self-discrimination processes. Elsevier 2023-07-17 /pmc/articles/PMC10392085/ /pubmed/37534169 http://dx.doi.org/10.1016/j.isci.2023.107238 Text en © 2023 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 Article
Kanadome, Takashi
Hoshino, Natsumi
Nagai, Takeharu
Yagi, Takeshi
Matsuda, Tomoki
Visualization of trans-interactions of a protocadherin-α between processes originating from single neurons
title Visualization of trans-interactions of a protocadherin-α between processes originating from single neurons
title_full Visualization of trans-interactions of a protocadherin-α between processes originating from single neurons
title_fullStr Visualization of trans-interactions of a protocadherin-α between processes originating from single neurons
title_full_unstemmed Visualization of trans-interactions of a protocadherin-α between processes originating from single neurons
title_short Visualization of trans-interactions of a protocadherin-α between processes originating from single neurons
title_sort visualization of trans-interactions of a protocadherin-α between processes originating from single neurons
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10392085/
https://www.ncbi.nlm.nih.gov/pubmed/37534169
http://dx.doi.org/10.1016/j.isci.2023.107238
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