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A neuroprotective astrocyte state is induced by neuronal signal EphB1 but fails in ALS models
Astrocyte responses to neuronal injury may be beneficial or detrimental to neuronal recovery, but the mechanisms that determine these different responses are poorly understood. Here we show that ephrin type-B receptor 1 (EphB1) is upregulated in injured motor neurons, which in turn can activate astr...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5660125/ https://www.ncbi.nlm.nih.gov/pubmed/29079839 http://dx.doi.org/10.1038/s41467-017-01283-z |
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author | Tyzack, Giulia E. Hall, Claire E. Sibley, Christopher R. Cymes, Tomasz Forostyak, Serhiy Carlino, Giulia Meyer, Ione F. Schiavo, Giampietro Zhang, Su-Chun Gibbons, George M. Newcombe, Jia Patani, Rickie Lakatos, András |
author_facet | Tyzack, Giulia E. Hall, Claire E. Sibley, Christopher R. Cymes, Tomasz Forostyak, Serhiy Carlino, Giulia Meyer, Ione F. Schiavo, Giampietro Zhang, Su-Chun Gibbons, George M. Newcombe, Jia Patani, Rickie Lakatos, András |
author_sort | Tyzack, Giulia E. |
collection | PubMed |
description | Astrocyte responses to neuronal injury may be beneficial or detrimental to neuronal recovery, but the mechanisms that determine these different responses are poorly understood. Here we show that ephrin type-B receptor 1 (EphB1) is upregulated in injured motor neurons, which in turn can activate astrocytes through ephrin-B1-mediated stimulation of signal transducer and activator of transcription-3 (STAT3). Transcriptional analysis shows that EphB1 induces a protective and anti-inflammatory signature in astrocytes, partially linked to the STAT3 network. This is distinct from the response evoked by interleukin (IL)-6 that is known to induce both pro inflammatory and anti-inflammatory processes. Finally, we demonstrate that the EphB1–ephrin-B1 pathway is disrupted in human stem cell derived astrocyte and mouse models of amyotrophic lateral sclerosis (ALS). Our work identifies an early neuronal help-me signal that activates a neuroprotective astrocytic response, which fails in ALS, and therefore represents an attractive therapeutic target. |
format | Online Article Text |
id | pubmed-5660125 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-56601252017-10-31 A neuroprotective astrocyte state is induced by neuronal signal EphB1 but fails in ALS models Tyzack, Giulia E. Hall, Claire E. Sibley, Christopher R. Cymes, Tomasz Forostyak, Serhiy Carlino, Giulia Meyer, Ione F. Schiavo, Giampietro Zhang, Su-Chun Gibbons, George M. Newcombe, Jia Patani, Rickie Lakatos, András Nat Commun Article Astrocyte responses to neuronal injury may be beneficial or detrimental to neuronal recovery, but the mechanisms that determine these different responses are poorly understood. Here we show that ephrin type-B receptor 1 (EphB1) is upregulated in injured motor neurons, which in turn can activate astrocytes through ephrin-B1-mediated stimulation of signal transducer and activator of transcription-3 (STAT3). Transcriptional analysis shows that EphB1 induces a protective and anti-inflammatory signature in astrocytes, partially linked to the STAT3 network. This is distinct from the response evoked by interleukin (IL)-6 that is known to induce both pro inflammatory and anti-inflammatory processes. Finally, we demonstrate that the EphB1–ephrin-B1 pathway is disrupted in human stem cell derived astrocyte and mouse models of amyotrophic lateral sclerosis (ALS). Our work identifies an early neuronal help-me signal that activates a neuroprotective astrocytic response, which fails in ALS, and therefore represents an attractive therapeutic target. Nature Publishing Group UK 2017-10-27 /pmc/articles/PMC5660125/ /pubmed/29079839 http://dx.doi.org/10.1038/s41467-017-01283-z Text en © The Author(s) 2017 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 Tyzack, Giulia E. Hall, Claire E. Sibley, Christopher R. Cymes, Tomasz Forostyak, Serhiy Carlino, Giulia Meyer, Ione F. Schiavo, Giampietro Zhang, Su-Chun Gibbons, George M. Newcombe, Jia Patani, Rickie Lakatos, András A neuroprotective astrocyte state is induced by neuronal signal EphB1 but fails in ALS models |
title | A neuroprotective astrocyte state is induced by neuronal signal EphB1 but fails in ALS models |
title_full | A neuroprotective astrocyte state is induced by neuronal signal EphB1 but fails in ALS models |
title_fullStr | A neuroprotective astrocyte state is induced by neuronal signal EphB1 but fails in ALS models |
title_full_unstemmed | A neuroprotective astrocyte state is induced by neuronal signal EphB1 but fails in ALS models |
title_short | A neuroprotective astrocyte state is induced by neuronal signal EphB1 but fails in ALS models |
title_sort | neuroprotective astrocyte state is induced by neuronal signal ephb1 but fails in als models |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5660125/ https://www.ncbi.nlm.nih.gov/pubmed/29079839 http://dx.doi.org/10.1038/s41467-017-01283-z |
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