The Generation and Functional Characterization of Human Microglia-Like Cells Derived from iPS and Embryonic Stem Cells.

Chemically defined differentiation Hematopoietic precursor cells Induced pluripotent stem (iPS) cells Microglia (iMG)

Journal

Methods in molecular biology (Clifton, N.J.)
ISSN: 1940-6029
Titre abrégé: Methods Mol Biol
Pays: United States
ID NLM: 9214969

Informations de publication

Date de publication:
2023
Historique:
medline: 12 6 2023
pubmed: 10 6 2023
entrez: 10 6 2023
Statut: ppublish

Résumé

The following protocol describes the generation of microglia cells from human-induced pluripotent stem cells (hiPSCs) using commercially available kits by StemCell Technologies. This protocol consists of three major steps: (1) Differentiation of hematopoietic precursor cells, (2) Microglia differentiation, and (3) Microglia maturation. Assays are described to characterize hematopoietic precursor cells and mature microglia.

Identifiants

pubmed: 37300767
doi: 10.1007/978-1-0716-3287-1_6
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

69-78

Subventions

Organisme : NIGMS NIH HHS
ID : P20 GM119943
Pays : United States
Organisme : NIA NIH HHS
ID : R21 AG077697
Pays : United States

Informations de copyright

© 2023. The Author(s), under exclusive license to Springer Science+Business Media, LLC, part of Springer Nature.

Références

Wurm J, Konttinen H, Andressen C et al (2021) Microglia development and maturation and its implications for induction of microglia-like cells from human iPSCs. Int J Mol Sci 22:3088
doi: 10.3390/ijms22063088 pubmed: 33803024 pmcid: 8002593
Abud E, Ramirez R, Martinez E et al (2017) iPSC-derived human microglia-like cells to study neurological diseases. Neuron 94(2):278–293
doi: 10.1016/j.neuron.2017.03.042 pubmed: 28426964 pmcid: 5482419
Guttikonda S, Sikkema L, Tchieu J et al (2021) Fully defined human pluripotent stem cell-derived microglia and tri-culture system model C3 production in Alzheimer’s disease. Nat Neurosci 24:343–354
doi: 10.1038/s41593-020-00796-z pubmed: 33558694 pmcid: 8382543

Auteurs

Mikael Lehoux (M)

Department of Molecular Biology, Cell Biology and Biochemistry, Center for Translational Neuroscience, Carney Institute for Brain Science and Brown Institute of Translational Science, Brown University, Providence, RI, USA.

Kevin Connolly (K)

Department of Molecular Biology, Cell Biology and Biochemistry, Center for Translational Neuroscience, Carney Institute for Brain Science and Brown Institute of Translational Science, Brown University, Providence, RI, USA.

Benedetta Assetta (B)

Department of Molecular Biology, Cell Biology and Biochemistry, Center for Translational Neuroscience, Carney Institute for Brain Science and Brown Institute of Translational Science, Brown University, Providence, RI, USA.

Yu-Wen Alvin Huang (YA)

Department of Molecular Biology, Cell Biology and Biochemistry, Center for Translational Neuroscience, Carney Institute for Brain Science and Brown Institute of Translational Science, Brown University, Providence, RI, USA. alvinhuang@brown.edu.

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Classifications MeSH