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Protocadherin 15 suppresses oligodendrocyte progenitor cell proliferation and promotes motility through distinct signalling pathways

Oligodendrocyte progenitor cells (OPCs) express protocadherin 15 (Pcdh15), a member of the cadherin superfamily of transmembrane proteins. Little is known about the function of Pcdh15 in the central nervous system (CNS), however, Pcdh15 expression can predict glioma aggression and promote the separa...

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Autores principales: Zhen, Yilan, Cullen, Carlie L., Ricci, Raphael, Summers, Benjamin S., Rehman, Sakina, Ahmed, Zubair M., Foster, Antoinette Y., Emery, Ben, Gasperini, Robert, Young, Kaylene M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9151716/
https://www.ncbi.nlm.nih.gov/pubmed/35637313
http://dx.doi.org/10.1038/s42003-022-03470-1
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author Zhen, Yilan
Cullen, Carlie L.
Ricci, Raphael
Summers, Benjamin S.
Rehman, Sakina
Ahmed, Zubair M.
Foster, Antoinette Y.
Emery, Ben
Gasperini, Robert
Young, Kaylene M.
author_facet Zhen, Yilan
Cullen, Carlie L.
Ricci, Raphael
Summers, Benjamin S.
Rehman, Sakina
Ahmed, Zubair M.
Foster, Antoinette Y.
Emery, Ben
Gasperini, Robert
Young, Kaylene M.
author_sort Zhen, Yilan
collection PubMed
description Oligodendrocyte progenitor cells (OPCs) express protocadherin 15 (Pcdh15), a member of the cadherin superfamily of transmembrane proteins. Little is known about the function of Pcdh15 in the central nervous system (CNS), however, Pcdh15 expression can predict glioma aggression and promote the separation of embryonic human OPCs immediately following a cell division. Herein, we show that Pcdh15 knockdown significantly increases extracellular signal-related kinase (ERK) phosphorylation and activation to enhance OPC proliferation in vitro. Furthermore, Pcdh15 knockdown elevates Cdc42-Arp2/3 signalling and impairs actin kinetics, reducing the frequency of lamellipodial extrusion and slowing filopodial withdrawal. Pcdh15 knockdown also reduces the number of processes supported by each OPC and new process generation. Our data indicate that Pcdh15 is a critical regulator of OPC proliferation and process motility, behaviours that characterise the function of these cells in the healthy CNS, and provide mechanistic insight into the role that Pcdh15 might play in glioma progression.
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spelling pubmed-91517162022-06-01 Protocadherin 15 suppresses oligodendrocyte progenitor cell proliferation and promotes motility through distinct signalling pathways Zhen, Yilan Cullen, Carlie L. Ricci, Raphael Summers, Benjamin S. Rehman, Sakina Ahmed, Zubair M. Foster, Antoinette Y. Emery, Ben Gasperini, Robert Young, Kaylene M. Commun Biol Article Oligodendrocyte progenitor cells (OPCs) express protocadherin 15 (Pcdh15), a member of the cadherin superfamily of transmembrane proteins. Little is known about the function of Pcdh15 in the central nervous system (CNS), however, Pcdh15 expression can predict glioma aggression and promote the separation of embryonic human OPCs immediately following a cell division. Herein, we show that Pcdh15 knockdown significantly increases extracellular signal-related kinase (ERK) phosphorylation and activation to enhance OPC proliferation in vitro. Furthermore, Pcdh15 knockdown elevates Cdc42-Arp2/3 signalling and impairs actin kinetics, reducing the frequency of lamellipodial extrusion and slowing filopodial withdrawal. Pcdh15 knockdown also reduces the number of processes supported by each OPC and new process generation. Our data indicate that Pcdh15 is a critical regulator of OPC proliferation and process motility, behaviours that characterise the function of these cells in the healthy CNS, and provide mechanistic insight into the role that Pcdh15 might play in glioma progression. Nature Publishing Group UK 2022-05-30 /pmc/articles/PMC9151716/ /pubmed/35637313 http://dx.doi.org/10.1038/s42003-022-03470-1 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Zhen, Yilan
Cullen, Carlie L.
Ricci, Raphael
Summers, Benjamin S.
Rehman, Sakina
Ahmed, Zubair M.
Foster, Antoinette Y.
Emery, Ben
Gasperini, Robert
Young, Kaylene M.
Protocadherin 15 suppresses oligodendrocyte progenitor cell proliferation and promotes motility through distinct signalling pathways
title Protocadherin 15 suppresses oligodendrocyte progenitor cell proliferation and promotes motility through distinct signalling pathways
title_full Protocadherin 15 suppresses oligodendrocyte progenitor cell proliferation and promotes motility through distinct signalling pathways
title_fullStr Protocadherin 15 suppresses oligodendrocyte progenitor cell proliferation and promotes motility through distinct signalling pathways
title_full_unstemmed Protocadherin 15 suppresses oligodendrocyte progenitor cell proliferation and promotes motility through distinct signalling pathways
title_short Protocadherin 15 suppresses oligodendrocyte progenitor cell proliferation and promotes motility through distinct signalling pathways
title_sort protocadherin 15 suppresses oligodendrocyte progenitor cell proliferation and promotes motility through distinct signalling pathways
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9151716/
https://www.ncbi.nlm.nih.gov/pubmed/35637313
http://dx.doi.org/10.1038/s42003-022-03470-1
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