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Microglia innately develop within cerebral organoids

Cerebral organoids are 3D stem cell-derived models that can be utilized to study the human brain. The current consensus is that cerebral organoids consist of cells derived from the neuroectodermal lineage. This limits their value and applicability, as mesodermal-derived microglia are important playe...

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Autores principales: Ormel, Paul R., Vieira de Sá, Renata, van Bodegraven, Emma J., Karst, Henk, Harschnitz, Oliver, Sneeboer, Marjolein A. M., Johansen, Lill Eva, van Dijk, Roland E., Scheefhals, Nicky, Berdenis van Berlekom, Amber, Ribes Martínez, Eduardo, Kling, Sandra, MacGillavry, Harold D., van den Berg, Leonard H., Kahn, René S., Hol, Elly M., de Witte, Lot D., Pasterkamp, R. Jeroen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6177485/
https://www.ncbi.nlm.nih.gov/pubmed/30301888
http://dx.doi.org/10.1038/s41467-018-06684-2
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author Ormel, Paul R.
Vieira de Sá, Renata
van Bodegraven, Emma J.
Karst, Henk
Harschnitz, Oliver
Sneeboer, Marjolein A. M.
Johansen, Lill Eva
van Dijk, Roland E.
Scheefhals, Nicky
Berdenis van Berlekom, Amber
Ribes Martínez, Eduardo
Kling, Sandra
MacGillavry, Harold D.
van den Berg, Leonard H.
Kahn, René S.
Hol, Elly M.
de Witte, Lot D.
Pasterkamp, R. Jeroen
author_facet Ormel, Paul R.
Vieira de Sá, Renata
van Bodegraven, Emma J.
Karst, Henk
Harschnitz, Oliver
Sneeboer, Marjolein A. M.
Johansen, Lill Eva
van Dijk, Roland E.
Scheefhals, Nicky
Berdenis van Berlekom, Amber
Ribes Martínez, Eduardo
Kling, Sandra
MacGillavry, Harold D.
van den Berg, Leonard H.
Kahn, René S.
Hol, Elly M.
de Witte, Lot D.
Pasterkamp, R. Jeroen
author_sort Ormel, Paul R.
collection PubMed
description Cerebral organoids are 3D stem cell-derived models that can be utilized to study the human brain. The current consensus is that cerebral organoids consist of cells derived from the neuroectodermal lineage. This limits their value and applicability, as mesodermal-derived microglia are important players in neural development and disease. Remarkably, here we show that microglia can innately develop within a cerebral organoid model and display their characteristic ramified morphology. The transcriptome and response to inflammatory stimulation of these organoid-grown microglia closely mimic the transcriptome and response of adult microglia acutely isolated from post mortem human brain tissue. In addition, organoid-grown microglia mediate phagocytosis and synaptic material is detected inside them. In all, our study characterizes a microglia-containing organoid model that represents a valuable tool for studying the interplay between microglia, macroglia, and neurons in human brain development and disease.
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spelling pubmed-61774852018-10-11 Microglia innately develop within cerebral organoids Ormel, Paul R. Vieira de Sá, Renata van Bodegraven, Emma J. Karst, Henk Harschnitz, Oliver Sneeboer, Marjolein A. M. Johansen, Lill Eva van Dijk, Roland E. Scheefhals, Nicky Berdenis van Berlekom, Amber Ribes Martínez, Eduardo Kling, Sandra MacGillavry, Harold D. van den Berg, Leonard H. Kahn, René S. Hol, Elly M. de Witte, Lot D. Pasterkamp, R. Jeroen Nat Commun Article Cerebral organoids are 3D stem cell-derived models that can be utilized to study the human brain. The current consensus is that cerebral organoids consist of cells derived from the neuroectodermal lineage. This limits their value and applicability, as mesodermal-derived microglia are important players in neural development and disease. Remarkably, here we show that microglia can innately develop within a cerebral organoid model and display their characteristic ramified morphology. The transcriptome and response to inflammatory stimulation of these organoid-grown microglia closely mimic the transcriptome and response of adult microglia acutely isolated from post mortem human brain tissue. In addition, organoid-grown microglia mediate phagocytosis and synaptic material is detected inside them. In all, our study characterizes a microglia-containing organoid model that represents a valuable tool for studying the interplay between microglia, macroglia, and neurons in human brain development and disease. Nature Publishing Group UK 2018-10-09 /pmc/articles/PMC6177485/ /pubmed/30301888 http://dx.doi.org/10.1038/s41467-018-06684-2 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Ormel, Paul R.
Vieira de Sá, Renata
van Bodegraven, Emma J.
Karst, Henk
Harschnitz, Oliver
Sneeboer, Marjolein A. M.
Johansen, Lill Eva
van Dijk, Roland E.
Scheefhals, Nicky
Berdenis van Berlekom, Amber
Ribes Martínez, Eduardo
Kling, Sandra
MacGillavry, Harold D.
van den Berg, Leonard H.
Kahn, René S.
Hol, Elly M.
de Witte, Lot D.
Pasterkamp, R. Jeroen
Microglia innately develop within cerebral organoids
title Microglia innately develop within cerebral organoids
title_full Microglia innately develop within cerebral organoids
title_fullStr Microglia innately develop within cerebral organoids
title_full_unstemmed Microglia innately develop within cerebral organoids
title_short Microglia innately develop within cerebral organoids
title_sort microglia innately develop within cerebral organoids
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6177485/
https://www.ncbi.nlm.nih.gov/pubmed/30301888
http://dx.doi.org/10.1038/s41467-018-06684-2
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