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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
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.
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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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