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Engrailed 1 coordinates cytoskeletal reorganization to induce myofibroblast differentiation

Transforming growth factor-β (TGFβ) is a key mediator of fibroblast activation in fibrotic diseases, including systemic sclerosis. Here we show that Engrailed 1 (EN1) is reexpressed in multiple fibroblast subpopulations in the skin of SSc patients. We characterize EN1 as a molecular amplifier of TGF...

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Autores principales: Györfi, Andrea-Hermina, Matei, Alexandru-Emil, Fuchs, Maximilian, Liang, Chunguang, Rigau, Aleix Rius, Hong, Xuezhi, Zhu, Honglin, Luber, Markus, Bergmann, Christina, Dees, Clara, Ludolph, Ingo, Horch, Raymund E., Distler, Oliver, Wang, Jiucun, Bengsch, Bertram, Schett, Georg, Kunz, Meik, Distler, Jörg H.W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Rockefeller University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8288503/
https://www.ncbi.nlm.nih.gov/pubmed/34259830
http://dx.doi.org/10.1084/jem.20201916
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author Györfi, Andrea-Hermina
Matei, Alexandru-Emil
Fuchs, Maximilian
Liang, Chunguang
Rigau, Aleix Rius
Hong, Xuezhi
Zhu, Honglin
Luber, Markus
Bergmann, Christina
Dees, Clara
Ludolph, Ingo
Horch, Raymund E.
Distler, Oliver
Wang, Jiucun
Bengsch, Bertram
Schett, Georg
Kunz, Meik
Distler, Jörg H.W.
author_facet Györfi, Andrea-Hermina
Matei, Alexandru-Emil
Fuchs, Maximilian
Liang, Chunguang
Rigau, Aleix Rius
Hong, Xuezhi
Zhu, Honglin
Luber, Markus
Bergmann, Christina
Dees, Clara
Ludolph, Ingo
Horch, Raymund E.
Distler, Oliver
Wang, Jiucun
Bengsch, Bertram
Schett, Georg
Kunz, Meik
Distler, Jörg H.W.
author_sort Györfi, Andrea-Hermina
collection PubMed
description Transforming growth factor-β (TGFβ) is a key mediator of fibroblast activation in fibrotic diseases, including systemic sclerosis. Here we show that Engrailed 1 (EN1) is reexpressed in multiple fibroblast subpopulations in the skin of SSc patients. We characterize EN1 as a molecular amplifier of TGFβ signaling in myofibroblast differentiation: TGFβ induces EN1 expression in a SMAD3-dependent manner, and in turn, EN1 mediates the profibrotic effects of TGFβ. RNA sequencing demonstrates that EN1 induces a profibrotic gene expression profile functionally related to cytoskeleton organization and ROCK activation. EN1 regulates gene expression by modulating the activity of SP1 and other SP transcription factors, as confirmed by ChIP-seq experiments for EN1 and SP1. Functional experiments confirm the coordinating role of EN1 on ROCK activity and the reorganization of cytoskeleton during myofibroblast differentiation, in both standard fibroblast culture systems and in vitro skin models. Consistently, mice with fibroblast-specific knockout of En1 demonstrate impaired fibroblast-to-myofibroblast transition and are partially protected from experimental skin fibrosis.
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spelling pubmed-82885032022-03-06 Engrailed 1 coordinates cytoskeletal reorganization to induce myofibroblast differentiation Györfi, Andrea-Hermina Matei, Alexandru-Emil Fuchs, Maximilian Liang, Chunguang Rigau, Aleix Rius Hong, Xuezhi Zhu, Honglin Luber, Markus Bergmann, Christina Dees, Clara Ludolph, Ingo Horch, Raymund E. Distler, Oliver Wang, Jiucun Bengsch, Bertram Schett, Georg Kunz, Meik Distler, Jörg H.W. J Exp Med Article Transforming growth factor-β (TGFβ) is a key mediator of fibroblast activation in fibrotic diseases, including systemic sclerosis. Here we show that Engrailed 1 (EN1) is reexpressed in multiple fibroblast subpopulations in the skin of SSc patients. We characterize EN1 as a molecular amplifier of TGFβ signaling in myofibroblast differentiation: TGFβ induces EN1 expression in a SMAD3-dependent manner, and in turn, EN1 mediates the profibrotic effects of TGFβ. RNA sequencing demonstrates that EN1 induces a profibrotic gene expression profile functionally related to cytoskeleton organization and ROCK activation. EN1 regulates gene expression by modulating the activity of SP1 and other SP transcription factors, as confirmed by ChIP-seq experiments for EN1 and SP1. Functional experiments confirm the coordinating role of EN1 on ROCK activity and the reorganization of cytoskeleton during myofibroblast differentiation, in both standard fibroblast culture systems and in vitro skin models. Consistently, mice with fibroblast-specific knockout of En1 demonstrate impaired fibroblast-to-myofibroblast transition and are partially protected from experimental skin fibrosis. Rockefeller University Press 2021-07-14 /pmc/articles/PMC8288503/ /pubmed/34259830 http://dx.doi.org/10.1084/jem.20201916 Text en © 2021 Györfi et al. http://www.rupress.org/terms/https://creativecommons.org/licenses/by-nc-sa/4.0/This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms/). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 International license, as described at https://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Article
Györfi, Andrea-Hermina
Matei, Alexandru-Emil
Fuchs, Maximilian
Liang, Chunguang
Rigau, Aleix Rius
Hong, Xuezhi
Zhu, Honglin
Luber, Markus
Bergmann, Christina
Dees, Clara
Ludolph, Ingo
Horch, Raymund E.
Distler, Oliver
Wang, Jiucun
Bengsch, Bertram
Schett, Georg
Kunz, Meik
Distler, Jörg H.W.
Engrailed 1 coordinates cytoskeletal reorganization to induce myofibroblast differentiation
title Engrailed 1 coordinates cytoskeletal reorganization to induce myofibroblast differentiation
title_full Engrailed 1 coordinates cytoskeletal reorganization to induce myofibroblast differentiation
title_fullStr Engrailed 1 coordinates cytoskeletal reorganization to induce myofibroblast differentiation
title_full_unstemmed Engrailed 1 coordinates cytoskeletal reorganization to induce myofibroblast differentiation
title_short Engrailed 1 coordinates cytoskeletal reorganization to induce myofibroblast differentiation
title_sort engrailed 1 coordinates cytoskeletal reorganization to induce myofibroblast differentiation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8288503/
https://www.ncbi.nlm.nih.gov/pubmed/34259830
http://dx.doi.org/10.1084/jem.20201916
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