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A positive feedback loop bi-stably activates fibroblasts
Although fibroblasts are dormant in normal tissue, they exhibit explosive activation during wound healing and perpetual activation in pathologic fibrosis and cancer stroma. The key regulatory network controlling these fibroblast dynamics is still unknown. Here, we report that Twist1, a key regulator...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6070563/ https://www.ncbi.nlm.nih.gov/pubmed/30069061 http://dx.doi.org/10.1038/s41467-018-05274-6 |
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author | Yeo, So-Young Lee, Keun-Woo Shin, Dongkwan An, Sugyun Cho, Kwang-Hyun Kim, Seok-Hyung |
author_facet | Yeo, So-Young Lee, Keun-Woo Shin, Dongkwan An, Sugyun Cho, Kwang-Hyun Kim, Seok-Hyung |
author_sort | Yeo, So-Young |
collection | PubMed |
description | Although fibroblasts are dormant in normal tissue, they exhibit explosive activation during wound healing and perpetual activation in pathologic fibrosis and cancer stroma. The key regulatory network controlling these fibroblast dynamics is still unknown. Here, we report that Twist1, a key regulator of cancer-associated fibroblasts, directly upregulates Prrx1, which, in turn, increases the expression of Tenascin-C (TNC). TNC also increases Twist1 expression, consequently forming a Twist1-Prrx1-TNC positive feedback loop (PFL). Systems biology studies reveal that the Twist1-Prrx1-TNC PFL can function as a bistable ON/OFF switch and regulates fibroblast activation. This PFL can be irreversibly activated under pathologic conditions, leading to perpetual fibroblast activation. Sustained activation of the Twist1-Prrx1-TNC PFL reproduces fibrotic nodules similar to idiopathic pulmonary fibrosis in vivo and is implicated in fibrotic disease and cancer stroma. Considering that this PFL is specific to activated fibroblasts, Twist1-Prrx1-TNC PFL may be a fibroblast-specific therapeutic target to deprogram perpetually activated fibroblasts. |
format | Online Article Text |
id | pubmed-6070563 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-60705632018-08-06 A positive feedback loop bi-stably activates fibroblasts Yeo, So-Young Lee, Keun-Woo Shin, Dongkwan An, Sugyun Cho, Kwang-Hyun Kim, Seok-Hyung Nat Commun Article Although fibroblasts are dormant in normal tissue, they exhibit explosive activation during wound healing and perpetual activation in pathologic fibrosis and cancer stroma. The key regulatory network controlling these fibroblast dynamics is still unknown. Here, we report that Twist1, a key regulator of cancer-associated fibroblasts, directly upregulates Prrx1, which, in turn, increases the expression of Tenascin-C (TNC). TNC also increases Twist1 expression, consequently forming a Twist1-Prrx1-TNC positive feedback loop (PFL). Systems biology studies reveal that the Twist1-Prrx1-TNC PFL can function as a bistable ON/OFF switch and regulates fibroblast activation. This PFL can be irreversibly activated under pathologic conditions, leading to perpetual fibroblast activation. Sustained activation of the Twist1-Prrx1-TNC PFL reproduces fibrotic nodules similar to idiopathic pulmonary fibrosis in vivo and is implicated in fibrotic disease and cancer stroma. Considering that this PFL is specific to activated fibroblasts, Twist1-Prrx1-TNC PFL may be a fibroblast-specific therapeutic target to deprogram perpetually activated fibroblasts. Nature Publishing Group UK 2018-08-01 /pmc/articles/PMC6070563/ /pubmed/30069061 http://dx.doi.org/10.1038/s41467-018-05274-6 Text en © The Author(s) 2018 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 Yeo, So-Young Lee, Keun-Woo Shin, Dongkwan An, Sugyun Cho, Kwang-Hyun Kim, Seok-Hyung A positive feedback loop bi-stably activates fibroblasts |
title | A positive feedback loop bi-stably activates fibroblasts |
title_full | A positive feedback loop bi-stably activates fibroblasts |
title_fullStr | A positive feedback loop bi-stably activates fibroblasts |
title_full_unstemmed | A positive feedback loop bi-stably activates fibroblasts |
title_short | A positive feedback loop bi-stably activates fibroblasts |
title_sort | positive feedback loop bi-stably activates fibroblasts |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6070563/ https://www.ncbi.nlm.nih.gov/pubmed/30069061 http://dx.doi.org/10.1038/s41467-018-05274-6 |
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