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The Colony Stimulating Factor-1 Receptor (CSF-1R)-Mediated Regulation of Microglia/Macrophages as a Target for Neurological Disorders (Glioma, Stroke)
Immunomodulatory therapies have fueled interest in targeting microglial cells as part of the innate immune response after infection or injury. In this context, the colony-stimulating factor 1 (CSF-1) and its receptor (CSF-1R) have gained attention in various neurological conditions to deplete and re...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8688767/ https://www.ncbi.nlm.nih.gov/pubmed/34950148 http://dx.doi.org/10.3389/fimmu.2021.787307 |
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author | Barca, Cristina Foray, Claudia Hermann, Sven Herrlinger, Ulrich Remory, Isabel Laoui, Damya Schäfers, Michael Grauer, Oliver M. Zinnhardt, Bastian Jacobs, Andreas H. |
author_facet | Barca, Cristina Foray, Claudia Hermann, Sven Herrlinger, Ulrich Remory, Isabel Laoui, Damya Schäfers, Michael Grauer, Oliver M. Zinnhardt, Bastian Jacobs, Andreas H. |
author_sort | Barca, Cristina |
collection | PubMed |
description | Immunomodulatory therapies have fueled interest in targeting microglial cells as part of the innate immune response after infection or injury. In this context, the colony-stimulating factor 1 (CSF-1) and its receptor (CSF-1R) have gained attention in various neurological conditions to deplete and reprogram the microglia/macrophages compartment. Published data in physiological conditions support the use of small-molecule inhibitors to study microglia/macrophages dynamics under inflammatory conditions and as a therapeutic strategy in pathologies where those cells support disease progression. However, preclinical and clinical data highlighted that the complexity of the spatiotemporal inflammatory response could limit their efficiency due to compensatory mechanisms, ultimately leading to therapy resistance. We review the current state-of-art in the field of CSF-1R inhibition in glioma and stroke and provide an overview of the fundamentals, ongoing research, potential developments of this promising therapeutic strategy and further application toward molecular imaging. |
format | Online Article Text |
id | pubmed-8688767 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-86887672021-12-22 The Colony Stimulating Factor-1 Receptor (CSF-1R)-Mediated Regulation of Microglia/Macrophages as a Target for Neurological Disorders (Glioma, Stroke) Barca, Cristina Foray, Claudia Hermann, Sven Herrlinger, Ulrich Remory, Isabel Laoui, Damya Schäfers, Michael Grauer, Oliver M. Zinnhardt, Bastian Jacobs, Andreas H. Front Immunol Immunology Immunomodulatory therapies have fueled interest in targeting microglial cells as part of the innate immune response after infection or injury. In this context, the colony-stimulating factor 1 (CSF-1) and its receptor (CSF-1R) have gained attention in various neurological conditions to deplete and reprogram the microglia/macrophages compartment. Published data in physiological conditions support the use of small-molecule inhibitors to study microglia/macrophages dynamics under inflammatory conditions and as a therapeutic strategy in pathologies where those cells support disease progression. However, preclinical and clinical data highlighted that the complexity of the spatiotemporal inflammatory response could limit their efficiency due to compensatory mechanisms, ultimately leading to therapy resistance. We review the current state-of-art in the field of CSF-1R inhibition in glioma and stroke and provide an overview of the fundamentals, ongoing research, potential developments of this promising therapeutic strategy and further application toward molecular imaging. Frontiers Media S.A. 2021-12-07 /pmc/articles/PMC8688767/ /pubmed/34950148 http://dx.doi.org/10.3389/fimmu.2021.787307 Text en Copyright © 2021 Barca, Foray, Hermann, Herrlinger, Remory, Laoui, Schäfers, Grauer, Zinnhardt and Jacobs 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 | Immunology Barca, Cristina Foray, Claudia Hermann, Sven Herrlinger, Ulrich Remory, Isabel Laoui, Damya Schäfers, Michael Grauer, Oliver M. Zinnhardt, Bastian Jacobs, Andreas H. The Colony Stimulating Factor-1 Receptor (CSF-1R)-Mediated Regulation of Microglia/Macrophages as a Target for Neurological Disorders (Glioma, Stroke) |
title | The Colony Stimulating Factor-1 Receptor (CSF-1R)-Mediated Regulation of Microglia/Macrophages as a Target for Neurological Disorders (Glioma, Stroke) |
title_full | The Colony Stimulating Factor-1 Receptor (CSF-1R)-Mediated Regulation of Microglia/Macrophages as a Target for Neurological Disorders (Glioma, Stroke) |
title_fullStr | The Colony Stimulating Factor-1 Receptor (CSF-1R)-Mediated Regulation of Microglia/Macrophages as a Target for Neurological Disorders (Glioma, Stroke) |
title_full_unstemmed | The Colony Stimulating Factor-1 Receptor (CSF-1R)-Mediated Regulation of Microglia/Macrophages as a Target for Neurological Disorders (Glioma, Stroke) |
title_short | The Colony Stimulating Factor-1 Receptor (CSF-1R)-Mediated Regulation of Microglia/Macrophages as a Target for Neurological Disorders (Glioma, Stroke) |
title_sort | colony stimulating factor-1 receptor (csf-1r)-mediated regulation of microglia/macrophages as a target for neurological disorders (glioma, stroke) |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8688767/ https://www.ncbi.nlm.nih.gov/pubmed/34950148 http://dx.doi.org/10.3389/fimmu.2021.787307 |
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