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Differentiation of human and murine induced pluripotent stem cells to microglia-like cells

Microglia are the resident inflammatory cells of the central nervous system (CNS) and have important roles in development, homeostasis and a variety of neurologic and psychiatric diseases. Difficulties in procuring human microglia have limited their study and hampered the clinical translation of mic...

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Autores principales: Pandya, Hetal, Shen, Michael J., Ichikawa, David M., Sedlock, Andrea B., Choi, Yong, Johnson, Kory R., Kim, Gloria, Brown, Mason A., Elkhaloun, Abdel G., Maric, Dragan, Sweeney, Colin L., Gossa, Selamawit, Malech, Harry L., McGavern, Dorian B., Park, John K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5404968/
https://www.ncbi.nlm.nih.gov/pubmed/28253233
http://dx.doi.org/10.1038/nn.4534
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author Pandya, Hetal
Shen, Michael J.
Ichikawa, David M.
Sedlock, Andrea B.
Choi, Yong
Johnson, Kory R.
Kim, Gloria
Brown, Mason A.
Elkhaloun, Abdel G.
Maric, Dragan
Sweeney, Colin L.
Gossa, Selamawit
Malech, Harry L.
McGavern, Dorian B.
Park, John K.
author_facet Pandya, Hetal
Shen, Michael J.
Ichikawa, David M.
Sedlock, Andrea B.
Choi, Yong
Johnson, Kory R.
Kim, Gloria
Brown, Mason A.
Elkhaloun, Abdel G.
Maric, Dragan
Sweeney, Colin L.
Gossa, Selamawit
Malech, Harry L.
McGavern, Dorian B.
Park, John K.
author_sort Pandya, Hetal
collection PubMed
description Microglia are the resident inflammatory cells of the central nervous system (CNS) and have important roles in development, homeostasis and a variety of neurologic and psychiatric diseases. Difficulties in procuring human microglia have limited their study and hampered the clinical translation of microglia-based treatments shown to be effective in animal disease models. Here, we report the differentiation of human induced pluripotent stem cells (iPSC) into microglia-like cells by exposure to defined factors and co-culture with astrocytes. These iPSC-derived microglia (iPS-MG) have the phenotype, gene expression profile and functional properties of brain-isolated microglia. Murine iPS-MG generated using a similar protocol have equivalent efficacy to primary brain-isolated microglia in the treatment of murine syngeneic intracranial malignant gliomas. The ability to generate human microglia facilitates the further study of this important CNS cell type and raises the possibility of their use in personalized medicine applications.
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spelling pubmed-54049682017-09-02 Differentiation of human and murine induced pluripotent stem cells to microglia-like cells Pandya, Hetal Shen, Michael J. Ichikawa, David M. Sedlock, Andrea B. Choi, Yong Johnson, Kory R. Kim, Gloria Brown, Mason A. Elkhaloun, Abdel G. Maric, Dragan Sweeney, Colin L. Gossa, Selamawit Malech, Harry L. McGavern, Dorian B. Park, John K. Nat Neurosci Article Microglia are the resident inflammatory cells of the central nervous system (CNS) and have important roles in development, homeostasis and a variety of neurologic and psychiatric diseases. Difficulties in procuring human microglia have limited their study and hampered the clinical translation of microglia-based treatments shown to be effective in animal disease models. Here, we report the differentiation of human induced pluripotent stem cells (iPSC) into microglia-like cells by exposure to defined factors and co-culture with astrocytes. These iPSC-derived microglia (iPS-MG) have the phenotype, gene expression profile and functional properties of brain-isolated microglia. Murine iPS-MG generated using a similar protocol have equivalent efficacy to primary brain-isolated microglia in the treatment of murine syngeneic intracranial malignant gliomas. The ability to generate human microglia facilitates the further study of this important CNS cell type and raises the possibility of their use in personalized medicine applications. 2017-03-02 2017-05 /pmc/articles/PMC5404968/ /pubmed/28253233 http://dx.doi.org/10.1038/nn.4534 Text en Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use: http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Pandya, Hetal
Shen, Michael J.
Ichikawa, David M.
Sedlock, Andrea B.
Choi, Yong
Johnson, Kory R.
Kim, Gloria
Brown, Mason A.
Elkhaloun, Abdel G.
Maric, Dragan
Sweeney, Colin L.
Gossa, Selamawit
Malech, Harry L.
McGavern, Dorian B.
Park, John K.
Differentiation of human and murine induced pluripotent stem cells to microglia-like cells
title Differentiation of human and murine induced pluripotent stem cells to microglia-like cells
title_full Differentiation of human and murine induced pluripotent stem cells to microglia-like cells
title_fullStr Differentiation of human and murine induced pluripotent stem cells to microglia-like cells
title_full_unstemmed Differentiation of human and murine induced pluripotent stem cells to microglia-like cells
title_short Differentiation of human and murine induced pluripotent stem cells to microglia-like cells
title_sort differentiation of human and murine induced pluripotent stem cells to microglia-like cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5404968/
https://www.ncbi.nlm.nih.gov/pubmed/28253233
http://dx.doi.org/10.1038/nn.4534
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