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

Detalhes bibliográficos
Autor(a) principal: Lourenço, T
Data de Publicação: 2016
Outros Autores: Faria, JP, Bippes, C, Maia, J, Lopes-Da-Silva, J, Relvas, JB, Graõs, M
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10216/108241
Resumo: 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 Modulation of oligodendrocyte differentiation and maturation by combined biochemical and mechanical cuesAtomic-force microscopyCell-differentiationMyosin-iiMorphological-differentiationExtracellular-matrixMultiple-sclerosisProgenitor cellsStem-cellsCNSSpecificationExtracellular 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 Group20162016-01-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfapplication/pdfhttp://hdl.handle.net/10216/108241eng2045-232210.1038/srep21563Lourenço, TFaria, JPBippes, CMaia, JLopes-Da-Silva, JRelvas, JBGraõs, Minfo:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2023-11-29T15:55:11Zoai:repositorio-aberto.up.pt:10216/108241Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-20T00:35:18.900339Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv 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
spellingShingle Modulation of oligodendrocyte differentiation and maturation by combined biochemical and mechanical cues
Lourenço, T
Atomic-force microscopy
Cell-differentiation
Myosin-ii
Morphological-differentiation
Extracellular-matrix
Multiple-sclerosis
Progenitor cells
Stem-cells
CNS
Specification
title_short 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_sort Modulation of oligodendrocyte differentiation and maturation by combined biochemical and mechanical cues
author Lourenço, T
author_facet Lourenço, T
Faria, JP
Bippes, C
Maia, J
Lopes-Da-Silva, J
Relvas, JB
Graõs, M
author_role author
author2 Faria, JP
Bippes, C
Maia, J
Lopes-Da-Silva, J
Relvas, JB
Graõs, M
author2_role author
author
author
author
author
author
dc.contributor.author.fl_str_mv Lourenço, T
Faria, JP
Bippes, C
Maia, J
Lopes-Da-Silva, J
Relvas, JB
Graõs, M
dc.subject.por.fl_str_mv Atomic-force microscopy
Cell-differentiation
Myosin-ii
Morphological-differentiation
Extracellular-matrix
Multiple-sclerosis
Progenitor cells
Stem-cells
CNS
Specification
topic Atomic-force microscopy
Cell-differentiation
Myosin-ii
Morphological-differentiation
Extracellular-matrix
Multiple-sclerosis
Progenitor cells
Stem-cells
CNS
Specification
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.
publishDate 2016
dc.date.none.fl_str_mv 2016
2016-01-01T00:00:00Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://hdl.handle.net/10216/108241
url http://hdl.handle.net/10216/108241
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 2045-2322
10.1038/srep21563
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
application/pdf
dc.publisher.none.fl_str_mv Nature Publishing Group
publisher.none.fl_str_mv Nature Publishing Group
dc.source.none.fl_str_mv reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
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instacron_str RCAAP
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reponame_str Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
collection Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
repository.name.fl_str_mv Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
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