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Modulation of oligodendrocyte differentiation and maturation by combined biochemical and mechanical cues

Extracellular matrix (ECM) proteins play a key role during oligodendrogenesis. While fibronectin (FN) is involved in the maintenance and proliferation of oligodendrocyte progenitor cells (OPCs), merosin (MN) promotes differentiation into oligodendrocytes (OLs). Mechanical properties of the ECM also...

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Autores principales: Lourenço, Tânia, Paes de Faria, Joana, Bippes, Christian A., Maia, João, Lopes-da-Silva, José A., Relvas, João B., Grãos, Mário
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4754901/
https://www.ncbi.nlm.nih.gov/pubmed/26879561
http://dx.doi.org/10.1038/srep21563
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author Lourenço, Tânia
Paes de Faria, Joana
Bippes, Christian A.
Maia, João
Lopes-da-Silva, José A.
Relvas, João B.
Grãos, Mário
author_facet Lourenço, Tânia
Paes de Faria, Joana
Bippes, Christian A.
Maia, João
Lopes-da-Silva, José A.
Relvas, João B.
Grãos, Mário
author_sort Lourenço, Tânia
collection PubMed
description Extracellular matrix (ECM) proteins play a key role during oligodendrogenesis. While fibronectin (FN) is involved in the maintenance and proliferation of oligodendrocyte progenitor cells (OPCs), merosin (MN) promotes differentiation into oligodendrocytes (OLs). Mechanical properties of the ECM also seem to affect OL differentiation, hence this study aimed to clarify the impact of combined biophysical and biochemical elements during oligodendrocyte differentiation and maturation using synthetic elastic polymeric ECM-like substrates. CG-4 cells presented OPC- or OL-like morphology in response to brain-compliant substrates functionalised with FN or MN, respectively. The expression of the differentiation and maturation markers myelin basic protein — MBP — and proteolipid protein — PLP — (respectively) by primary rat oligodendrocytes was enhanced in presence of MN, but only on brain-compliant conditions, considering the distribution (MBP) or amount (PLP) of the protein. It was also observed that maturation of OLs was attained earlier (by assessing PLP expression) by cells differentiated on MN-functionalised brain-compliant substrates than on standard culture conditions. Moreover, the combination of MN and substrate compliance enhanced the maturation and morphological complexity of OLs. Considering the distinct degrees of stiffness tested ranging within those of the central nervous system, our results indicate that 6.5 kPa is the most suitable rigidity for oligodendrocyte differentiation.
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spelling pubmed-47549012016-02-24 Modulation of oligodendrocyte differentiation and maturation by combined biochemical and mechanical cues Lourenço, Tânia Paes de Faria, Joana Bippes, Christian A. Maia, João Lopes-da-Silva, José A. Relvas, João B. Grãos, Mário Sci Rep Article Extracellular matrix (ECM) proteins play a key role during oligodendrogenesis. While fibronectin (FN) is involved in the maintenance and proliferation of oligodendrocyte progenitor cells (OPCs), merosin (MN) promotes differentiation into oligodendrocytes (OLs). Mechanical properties of the ECM also seem to affect OL differentiation, hence this study aimed to clarify the impact of combined biophysical and biochemical elements during oligodendrocyte differentiation and maturation using synthetic elastic polymeric ECM-like substrates. CG-4 cells presented OPC- or OL-like morphology in response to brain-compliant substrates functionalised with FN or MN, respectively. The expression of the differentiation and maturation markers myelin basic protein — MBP — and proteolipid protein — PLP — (respectively) by primary rat oligodendrocytes was enhanced in presence of MN, but only on brain-compliant conditions, considering the distribution (MBP) or amount (PLP) of the protein. It was also observed that maturation of OLs was attained earlier (by assessing PLP expression) by cells differentiated on MN-functionalised brain-compliant substrates than on standard culture conditions. Moreover, the combination of MN and substrate compliance enhanced the maturation and morphological complexity of OLs. Considering the distinct degrees of stiffness tested ranging within those of the central nervous system, our results indicate that 6.5 kPa is the most suitable rigidity for oligodendrocyte differentiation. Nature Publishing Group 2016-02-16 /pmc/articles/PMC4754901/ /pubmed/26879561 http://dx.doi.org/10.1038/srep21563 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Lourenço, Tânia
Paes de Faria, Joana
Bippes, Christian A.
Maia, João
Lopes-da-Silva, José A.
Relvas, João B.
Grãos, Mário
Modulation of oligodendrocyte differentiation and maturation by combined biochemical and mechanical cues
title Modulation of oligodendrocyte differentiation and maturation by combined biochemical and mechanical cues
title_full Modulation of oligodendrocyte differentiation and maturation by combined biochemical and mechanical cues
title_fullStr Modulation of oligodendrocyte differentiation and maturation by combined biochemical and mechanical cues
title_full_unstemmed Modulation of oligodendrocyte differentiation and maturation by combined biochemical and mechanical cues
title_short Modulation of oligodendrocyte differentiation and maturation by combined biochemical and mechanical cues
title_sort modulation of oligodendrocyte differentiation and maturation by combined biochemical and mechanical cues
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4754901/
https://www.ncbi.nlm.nih.gov/pubmed/26879561
http://dx.doi.org/10.1038/srep21563
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