Cargando…
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...
Autores principales: | , , , , , , , , , , |
---|---|
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 |
_version_ | 1783347770492452864 |
---|---|
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. |
format | Online Article Text |
id | pubmed-6094163 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT simaodaniel recapitulationofhumanneuralmicroenvironmentsignaturesinipscderivednpc3ddifferentiation AT silvamartam recapitulationofhumanneuralmicroenvironmentsignaturesinipscderivednpc3ddifferentiation AT terrassoanap recapitulationofhumanneuralmicroenvironmentsignaturesinipscderivednpc3ddifferentiation AT arezfrancisca recapitulationofhumanneuralmicroenvironmentsignaturesinipscderivednpc3ddifferentiation AT sousamarcosfq recapitulationofhumanneuralmicroenvironmentsignaturesinipscderivednpc3ddifferentiation AT mehrjardinargesz recapitulationofhumanneuralmicroenvironmentsignaturesinipscderivednpc3ddifferentiation AT sarictomo recapitulationofhumanneuralmicroenvironmentsignaturesinipscderivednpc3ddifferentiation AT gomesalvespatricia recapitulationofhumanneuralmicroenvironmentsignaturesinipscderivednpc3ddifferentiation AT raimundonuno recapitulationofhumanneuralmicroenvironmentsignaturesinipscderivednpc3ddifferentiation AT alvespaulam recapitulationofhumanneuralmicroenvironmentsignaturesinipscderivednpc3ddifferentiation AT britocatarina recapitulationofhumanneuralmicroenvironmentsignaturesinipscderivednpc3ddifferentiation |