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Peroxisomal defects in microglial cells induce a disease-associated microglial signature
Microglial cells ensure essential roles in brain homeostasis. In pathological condition, microglia adopt a common signature, called disease-associated microglial (DAM) signature, characterized by the loss of homeostatic genes and the induction of disease-associated genes. In X-linked adrenoleukodyst...
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10149961/ https://www.ncbi.nlm.nih.gov/pubmed/37138705 http://dx.doi.org/10.3389/fnmol.2023.1170313 |
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author | Raas, Quentin Tawbeh, Ali Tahri-Joutey, Mounia Gondcaille, Catherine Keime, Céline Kaiser, Romain Trompier, Doriane Nasser, Boubker Leoni, Valerio Bellanger, Emma Boussand, Maud Hamon, Yannick Benani, Alexandre Di Cara, Francesca Truntzer, Caroline Cherkaoui-Malki, Mustapha Andreoletti, Pierre Savary, Stéphane |
author_facet | Raas, Quentin Tawbeh, Ali Tahri-Joutey, Mounia Gondcaille, Catherine Keime, Céline Kaiser, Romain Trompier, Doriane Nasser, Boubker Leoni, Valerio Bellanger, Emma Boussand, Maud Hamon, Yannick Benani, Alexandre Di Cara, Francesca Truntzer, Caroline Cherkaoui-Malki, Mustapha Andreoletti, Pierre Savary, Stéphane |
author_sort | Raas, Quentin |
collection | PubMed |
description | Microglial cells ensure essential roles in brain homeostasis. In pathological condition, microglia adopt a common signature, called disease-associated microglial (DAM) signature, characterized by the loss of homeostatic genes and the induction of disease-associated genes. In X-linked adrenoleukodystrophy (X-ALD), the most common peroxisomal disease, microglial defect has been shown to precede myelin degradation and may actively contribute to the neurodegenerative process. We previously established BV-2 microglial cell models bearing mutations in peroxisomal genes that recapitulate some of the hallmarks of the peroxisomal β-oxidation defects such as very long-chain fatty acid (VLCFA) accumulation. In these cell lines, we used RNA-sequencing and identified large-scale reprogramming for genes involved in lipid metabolism, immune response, cell signaling, lysosome and autophagy, as well as a DAM-like signature. We highlighted cholesterol accumulation in plasma membranes and observed autophagy patterns in the cell mutants. We confirmed the upregulation or downregulation at the protein level for a few selected genes that mostly corroborated our observations and clearly demonstrated increased expression and secretion of DAM proteins in the BV-2 mutant cells. In conclusion, the peroxisomal defects in microglial cells not only impact on VLCFA metabolism but also force microglial cells to adopt a pathological phenotype likely representing a key contributor to the pathogenesis of peroxisomal disorders. |
format | Online Article Text |
id | pubmed-10149961 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-101499612023-05-02 Peroxisomal defects in microglial cells induce a disease-associated microglial signature Raas, Quentin Tawbeh, Ali Tahri-Joutey, Mounia Gondcaille, Catherine Keime, Céline Kaiser, Romain Trompier, Doriane Nasser, Boubker Leoni, Valerio Bellanger, Emma Boussand, Maud Hamon, Yannick Benani, Alexandre Di Cara, Francesca Truntzer, Caroline Cherkaoui-Malki, Mustapha Andreoletti, Pierre Savary, Stéphane Front Mol Neurosci Molecular Neuroscience Microglial cells ensure essential roles in brain homeostasis. In pathological condition, microglia adopt a common signature, called disease-associated microglial (DAM) signature, characterized by the loss of homeostatic genes and the induction of disease-associated genes. In X-linked adrenoleukodystrophy (X-ALD), the most common peroxisomal disease, microglial defect has been shown to precede myelin degradation and may actively contribute to the neurodegenerative process. We previously established BV-2 microglial cell models bearing mutations in peroxisomal genes that recapitulate some of the hallmarks of the peroxisomal β-oxidation defects such as very long-chain fatty acid (VLCFA) accumulation. In these cell lines, we used RNA-sequencing and identified large-scale reprogramming for genes involved in lipid metabolism, immune response, cell signaling, lysosome and autophagy, as well as a DAM-like signature. We highlighted cholesterol accumulation in plasma membranes and observed autophagy patterns in the cell mutants. We confirmed the upregulation or downregulation at the protein level for a few selected genes that mostly corroborated our observations and clearly demonstrated increased expression and secretion of DAM proteins in the BV-2 mutant cells. In conclusion, the peroxisomal defects in microglial cells not only impact on VLCFA metabolism but also force microglial cells to adopt a pathological phenotype likely representing a key contributor to the pathogenesis of peroxisomal disorders. Frontiers Media S.A. 2023-04-17 /pmc/articles/PMC10149961/ /pubmed/37138705 http://dx.doi.org/10.3389/fnmol.2023.1170313 Text en Copyright © 2023 Raas, Tawbeh, Tahri-Joutey, Gondcaille, Keime, Kaiser, Trompier, Nasser, Leoni, Bellanger, Boussand, Hamon, Benani, Di Cara, Truntzer, Cherkaoui-Malki, Andreoletti and Savary. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Molecular Neuroscience Raas, Quentin Tawbeh, Ali Tahri-Joutey, Mounia Gondcaille, Catherine Keime, Céline Kaiser, Romain Trompier, Doriane Nasser, Boubker Leoni, Valerio Bellanger, Emma Boussand, Maud Hamon, Yannick Benani, Alexandre Di Cara, Francesca Truntzer, Caroline Cherkaoui-Malki, Mustapha Andreoletti, Pierre Savary, Stéphane Peroxisomal defects in microglial cells induce a disease-associated microglial signature |
title | Peroxisomal defects in microglial cells induce a disease-associated microglial signature |
title_full | Peroxisomal defects in microglial cells induce a disease-associated microglial signature |
title_fullStr | Peroxisomal defects in microglial cells induce a disease-associated microglial signature |
title_full_unstemmed | Peroxisomal defects in microglial cells induce a disease-associated microglial signature |
title_short | Peroxisomal defects in microglial cells induce a disease-associated microglial signature |
title_sort | peroxisomal defects in microglial cells induce a disease-associated microglial signature |
topic | Molecular Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10149961/ https://www.ncbi.nlm.nih.gov/pubmed/37138705 http://dx.doi.org/10.3389/fnmol.2023.1170313 |
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