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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.
Afiliação
  • Peteri UK; Faculty of Medicine, Department of Physiology, University of Helsinki, P.O. Box 63, FI-00290 Helsinki, Finland.
  • Pitkonen J; Faculty of Medicine, Department of Physiology, University of Helsinki, P.O. Box 63, FI-00290 Helsinki, Finland.
  • Utami KH; Translational Laboratory in Genetic Medicine, Agency for Science, Technology and Research, Singapore (A*STAR), 8A Biomedical Grove, Immunos, Level 5, Singapore 138648, Singapore.
  • Paavola J; Minerva Foundation Institute for Medical Research, Biomedicum 2U, Tukholmankatu 8, FI-00290 Helsinki, Finland.
  • Roybon L; Stem Cell Laboratory for CNS Disease Modeling, Department of Experimental Medical Science, Lund University, SE-221 84 Lund, Sweden.
  • Pouladi MA; MultiPark and the Lund Stem Cell Center, Lund University, SE-221 84 Lund, Sweden.
  • Castrén ML; Translational Laboratory in Genetic Medicine, Agency for Science, Technology and Research, Singapore (A*STAR), 8A Biomedical Grove, Immunos, Level 5, Singapore 138648, Singapore.
Brain Sci ; 11(2)2021 Feb 09.
Article em En | MEDLINE | ID: mdl-33572154
ABSTRACT
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 S100ß. 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.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Revista: Brain Sci Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Finlândia

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Revista: Brain Sci Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Finlândia