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SFRP1 modulates astrocyte‐to‐microglia crosstalk in acute and chronic neuroinflammation
Neuroinflammation is a common feature of many neurodegenerative diseases. It fosters a dysfunctional neuron–microglia–astrocyte crosstalk that, in turn, maintains microglial cells in a perniciously reactive state that often enhances neuronal damage. The molecular components that mediate this critica...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8567217/ https://www.ncbi.nlm.nih.gov/pubmed/34569685 http://dx.doi.org/10.15252/embr.202051696 |
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author | Rueda‐Carrasco, Javier Martin‐Bermejo, María Jesús Pereyra, Guadalupe Mateo, María Inés Borroto, Aldo Brosseron, Frederic Kummer, Markus P Schwartz, Stephanie López‐Atalaya, José P Alarcon, Balbino Esteve, Pilar Heneka, Michael T Bovolenta, Paola |
author_facet | Rueda‐Carrasco, Javier Martin‐Bermejo, María Jesús Pereyra, Guadalupe Mateo, María Inés Borroto, Aldo Brosseron, Frederic Kummer, Markus P Schwartz, Stephanie López‐Atalaya, José P Alarcon, Balbino Esteve, Pilar Heneka, Michael T Bovolenta, Paola |
author_sort | Rueda‐Carrasco, Javier |
collection | PubMed |
description | Neuroinflammation is a common feature of many neurodegenerative diseases. It fosters a dysfunctional neuron–microglia–astrocyte crosstalk that, in turn, maintains microglial cells in a perniciously reactive state that often enhances neuronal damage. The molecular components that mediate this critical communication are not fully explored. Here, we show that secreted frizzled‐related protein 1 (SFRP1), a multifunctional regulator of cell‐to‐cell communication, is part of the cellular crosstalk underlying neuroinflammation. In mouse models of acute and chronic neuroinflammation, SFRP1, largely astrocyte‐derived, promotes and sustains microglial activation, and thus a chronic inflammatory state. SFRP1 promotes the upregulation of components of the hypoxia‐induced factor‐dependent inflammatory pathway and, to a lower extent, of those downstream of the nuclear factor‐kappa B. We thus propose that SFRP1 acts as an astrocyte‐to‐microglia amplifier of neuroinflammation, representing a potential valuable therapeutic target for counteracting the harmful effect of chronic inflammation in several neurodegenerative diseases. |
format | Online Article Text |
id | pubmed-8567217 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-85672172021-11-12 SFRP1 modulates astrocyte‐to‐microglia crosstalk in acute and chronic neuroinflammation Rueda‐Carrasco, Javier Martin‐Bermejo, María Jesús Pereyra, Guadalupe Mateo, María Inés Borroto, Aldo Brosseron, Frederic Kummer, Markus P Schwartz, Stephanie López‐Atalaya, José P Alarcon, Balbino Esteve, Pilar Heneka, Michael T Bovolenta, Paola EMBO Rep Articles Neuroinflammation is a common feature of many neurodegenerative diseases. It fosters a dysfunctional neuron–microglia–astrocyte crosstalk that, in turn, maintains microglial cells in a perniciously reactive state that often enhances neuronal damage. The molecular components that mediate this critical communication are not fully explored. Here, we show that secreted frizzled‐related protein 1 (SFRP1), a multifunctional regulator of cell‐to‐cell communication, is part of the cellular crosstalk underlying neuroinflammation. In mouse models of acute and chronic neuroinflammation, SFRP1, largely astrocyte‐derived, promotes and sustains microglial activation, and thus a chronic inflammatory state. SFRP1 promotes the upregulation of components of the hypoxia‐induced factor‐dependent inflammatory pathway and, to a lower extent, of those downstream of the nuclear factor‐kappa B. We thus propose that SFRP1 acts as an astrocyte‐to‐microglia amplifier of neuroinflammation, representing a potential valuable therapeutic target for counteracting the harmful effect of chronic inflammation in several neurodegenerative diseases. John Wiley and Sons Inc. 2021-09-27 2021-11-04 /pmc/articles/PMC8567217/ /pubmed/34569685 http://dx.doi.org/10.15252/embr.202051696 Text en © 2021 The Authors. Published under the terms of the CC BY NC ND 4.0 license https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Articles Rueda‐Carrasco, Javier Martin‐Bermejo, María Jesús Pereyra, Guadalupe Mateo, María Inés Borroto, Aldo Brosseron, Frederic Kummer, Markus P Schwartz, Stephanie López‐Atalaya, José P Alarcon, Balbino Esteve, Pilar Heneka, Michael T Bovolenta, Paola SFRP1 modulates astrocyte‐to‐microglia crosstalk in acute and chronic neuroinflammation |
title | SFRP1 modulates astrocyte‐to‐microglia crosstalk in acute and chronic neuroinflammation |
title_full | SFRP1 modulates astrocyte‐to‐microglia crosstalk in acute and chronic neuroinflammation |
title_fullStr | SFRP1 modulates astrocyte‐to‐microglia crosstalk in acute and chronic neuroinflammation |
title_full_unstemmed | SFRP1 modulates astrocyte‐to‐microglia crosstalk in acute and chronic neuroinflammation |
title_short | SFRP1 modulates astrocyte‐to‐microglia crosstalk in acute and chronic neuroinflammation |
title_sort | sfrp1 modulates astrocyte‐to‐microglia crosstalk in acute and chronic neuroinflammation |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8567217/ https://www.ncbi.nlm.nih.gov/pubmed/34569685 http://dx.doi.org/10.15252/embr.202051696 |
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