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Generation of the Human Pluripotent Stem-Cell-Derived Astrocyte Model with Forebrain Identity
Astrocytes form functionally and morphologically distinct populations of cells with brain-region-specific properties. Human pluripotent stem cells (hPSCs) offer possibilities to generate astroglia for studies investigating mechanisms governing the emergence of astrocytic diversity. We established a...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7914711/ https://www.ncbi.nlm.nih.gov/pubmed/33572154 http://dx.doi.org/10.3390/brainsci11020209 |
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author | Peteri, Ulla-Kaisa Pitkonen, Juho Utami, Kagistia Hana Paavola, Jere Roybon, Laurent Pouladi, Mahmoud A. Castrén, Maija L. |
author_facet | Peteri, Ulla-Kaisa Pitkonen, Juho Utami, Kagistia Hana Paavola, Jere Roybon, Laurent Pouladi, Mahmoud A. Castrén, Maija L. |
author_sort | Peteri, Ulla-Kaisa |
collection | PubMed |
description | Astrocytes form functionally and morphologically distinct populations of cells with brain-region-specific properties. Human pluripotent stem cells (hPSCs) offer possibilities to generate astroglia for studies investigating mechanisms governing the emergence of astrocytic diversity. We established a method to generate human astrocytes from hPSCs with forebrain patterning and final specification with ciliary neurotrophic factor (CNTF). Transcriptome profiling and gene enrichment analysis monitored the sequential expression of genes determining astrocyte differentiation and confirmed activation of forebrain differentiation pathways at Day 30 (D30) and D60 of differentiation in vitro. More than 90% of astrocytes aged D95 in vitro co-expressed the astrocytic markers glial fibrillary acidic protein (GFAP) and S100β. Intracellular calcium responses to ATP indicated differentiation of the functional astrocyte population with constitutive monocyte chemoattractant protein-1 (MCP-1/CCL2) and tissue inhibitor of metalloproteinases-2 (TIMP-2) expression. The method was reproducible across several hPSC lines, and the data demonstrated the usefulness of forebrain astrocyte modeling in research investigating forebrain pathology. |
format | Online Article Text |
id | pubmed-7914711 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-79147112021-03-01 Generation of the Human Pluripotent Stem-Cell-Derived Astrocyte Model with Forebrain Identity Peteri, Ulla-Kaisa Pitkonen, Juho Utami, Kagistia Hana Paavola, Jere Roybon, Laurent Pouladi, Mahmoud A. Castrén, Maija L. Brain Sci Article Astrocytes form functionally and morphologically distinct populations of cells with brain-region-specific properties. Human pluripotent stem cells (hPSCs) offer possibilities to generate astroglia for studies investigating mechanisms governing the emergence of astrocytic diversity. We established a method to generate human astrocytes from hPSCs with forebrain patterning and final specification with ciliary neurotrophic factor (CNTF). Transcriptome profiling and gene enrichment analysis monitored the sequential expression of genes determining astrocyte differentiation and confirmed activation of forebrain differentiation pathways at Day 30 (D30) and D60 of differentiation in vitro. More than 90% of astrocytes aged D95 in vitro co-expressed the astrocytic markers glial fibrillary acidic protein (GFAP) and S100β. Intracellular calcium responses to ATP indicated differentiation of the functional astrocyte population with constitutive monocyte chemoattractant protein-1 (MCP-1/CCL2) and tissue inhibitor of metalloproteinases-2 (TIMP-2) expression. The method was reproducible across several hPSC lines, and the data demonstrated the usefulness of forebrain astrocyte modeling in research investigating forebrain pathology. MDPI 2021-02-09 /pmc/articles/PMC7914711/ /pubmed/33572154 http://dx.doi.org/10.3390/brainsci11020209 Text en © 2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Peteri, Ulla-Kaisa Pitkonen, Juho Utami, Kagistia Hana Paavola, Jere Roybon, Laurent Pouladi, Mahmoud A. Castrén, Maija L. Generation of the Human Pluripotent Stem-Cell-Derived Astrocyte Model with Forebrain Identity |
title | Generation of the Human Pluripotent Stem-Cell-Derived Astrocyte Model with Forebrain Identity |
title_full | Generation of the Human Pluripotent Stem-Cell-Derived Astrocyte Model with Forebrain Identity |
title_fullStr | Generation of the Human Pluripotent Stem-Cell-Derived Astrocyte Model with Forebrain Identity |
title_full_unstemmed | Generation of the Human Pluripotent Stem-Cell-Derived Astrocyte Model with Forebrain Identity |
title_short | Generation of the Human Pluripotent Stem-Cell-Derived Astrocyte Model with Forebrain Identity |
title_sort | generation of the human pluripotent stem-cell-derived astrocyte model with forebrain identity |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7914711/ https://www.ncbi.nlm.nih.gov/pubmed/33572154 http://dx.doi.org/10.3390/brainsci11020209 |
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