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Recapitulation of Human Neural Microenvironment Signatures in iPSC-Derived NPC 3D Differentiation

Brain microenvironment plays an important role in neurodevelopment and pathology, where the extracellular matrix (ECM) and soluble factors modulate multiple cellular processes. Neural cell culture typically relies on heterologous matrices poorly resembling brain ECM. Here, we employed neurospheroids...

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Detalles Bibliográficos
Autores principales: Simão, Daniel, Silva, Marta M., Terrasso, Ana P., Arez, Francisca, Sousa, Marcos F.Q., Mehrjardi, Narges Z., Šarić, Tomo, Gomes-Alves, Patrícia, Raimundo, Nuno, Alves, Paula M., Brito, Catarina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6094163/
https://www.ncbi.nlm.nih.gov/pubmed/30057262
http://dx.doi.org/10.1016/j.stemcr.2018.06.020
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author Simão, Daniel
Silva, Marta M.
Terrasso, Ana P.
Arez, Francisca
Sousa, Marcos F.Q.
Mehrjardi, Narges Z.
Šarić, Tomo
Gomes-Alves, Patrícia
Raimundo, Nuno
Alves, Paula M.
Brito, Catarina
author_facet Simão, Daniel
Silva, Marta M.
Terrasso, Ana P.
Arez, Francisca
Sousa, Marcos F.Q.
Mehrjardi, Narges Z.
Šarić, Tomo
Gomes-Alves, Patrícia
Raimundo, Nuno
Alves, Paula M.
Brito, Catarina
author_sort Simão, Daniel
collection PubMed
description Brain microenvironment plays an important role in neurodevelopment and pathology, where the extracellular matrix (ECM) and soluble factors modulate multiple cellular processes. Neural cell culture typically relies on heterologous matrices poorly resembling brain ECM. Here, we employed neurospheroids to address microenvironment remodeling during neural differentiation of human stem cells, without the confounding effects of exogenous matrices. Proteome and transcriptome dynamics revealed significant changes at cell membrane and ECM during 3D differentiation, diverging significantly from the 2D differentiation. Structural proteoglycans typical of brain ECM were enriched during 3D differentiation, in contrast to basement membrane constituents in 2D. Moreover, higher expression of synaptic and ion transport machinery was observed in 3D cultures, suggesting higher neuronal maturation in neurospheroids. This work demonstrates that 3D neural differentiation as neurospheroids promotes the expression of cellular and extracellular features found in neural tissue, highlighting its value to address molecular defects in cell-ECM interactions associated with neurological disorders.
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spelling pubmed-60941632018-08-16 Recapitulation of Human Neural Microenvironment Signatures in iPSC-Derived NPC 3D Differentiation Simão, Daniel Silva, Marta M. Terrasso, Ana P. Arez, Francisca Sousa, Marcos F.Q. Mehrjardi, Narges Z. Šarić, Tomo Gomes-Alves, Patrícia Raimundo, Nuno Alves, Paula M. Brito, Catarina Stem Cell Reports Resource Brain microenvironment plays an important role in neurodevelopment and pathology, where the extracellular matrix (ECM) and soluble factors modulate multiple cellular processes. Neural cell culture typically relies on heterologous matrices poorly resembling brain ECM. Here, we employed neurospheroids to address microenvironment remodeling during neural differentiation of human stem cells, without the confounding effects of exogenous matrices. Proteome and transcriptome dynamics revealed significant changes at cell membrane and ECM during 3D differentiation, diverging significantly from the 2D differentiation. Structural proteoglycans typical of brain ECM were enriched during 3D differentiation, in contrast to basement membrane constituents in 2D. Moreover, higher expression of synaptic and ion transport machinery was observed in 3D cultures, suggesting higher neuronal maturation in neurospheroids. This work demonstrates that 3D neural differentiation as neurospheroids promotes the expression of cellular and extracellular features found in neural tissue, highlighting its value to address molecular defects in cell-ECM interactions associated with neurological disorders. Elsevier 2018-08-14 /pmc/articles/PMC6094163/ /pubmed/30057262 http://dx.doi.org/10.1016/j.stemcr.2018.06.020 Text en © 2018 The Authors http://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 Resource
Simão, Daniel
Silva, Marta M.
Terrasso, Ana P.
Arez, Francisca
Sousa, Marcos F.Q.
Mehrjardi, Narges Z.
Šarić, Tomo
Gomes-Alves, Patrícia
Raimundo, Nuno
Alves, Paula M.
Brito, Catarina
Recapitulation of Human Neural Microenvironment Signatures in iPSC-Derived NPC 3D Differentiation
title Recapitulation of Human Neural Microenvironment Signatures in iPSC-Derived NPC 3D Differentiation
title_full Recapitulation of Human Neural Microenvironment Signatures in iPSC-Derived NPC 3D Differentiation
title_fullStr Recapitulation of Human Neural Microenvironment Signatures in iPSC-Derived NPC 3D Differentiation
title_full_unstemmed Recapitulation of Human Neural Microenvironment Signatures in iPSC-Derived NPC 3D Differentiation
title_short Recapitulation of Human Neural Microenvironment Signatures in iPSC-Derived NPC 3D Differentiation
title_sort recapitulation of human neural microenvironment signatures in ipsc-derived npc 3d differentiation
topic Resource
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6094163/
https://www.ncbi.nlm.nih.gov/pubmed/30057262
http://dx.doi.org/10.1016/j.stemcr.2018.06.020
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