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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...
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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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. |
format | Online Article Text |
id | pubmed-6177485 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
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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