Activation of JUN in fibroblasts promotes pro-fibrotic programme and modulates protective immunity

Fibroblast contributions to lung fibrosis and in particular their crosstalk with immune cells in the lung are incompletely understood. Here, the authors show an overall immune suppressive environment transcriptionally controlled and maintained by fibroblasts in lung fibrosis with possible therapeuti...

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Main Authors: Lu Cui, Shih-Yu Chen, Tristan Lerbs, Jin-Wook Lee, Pablo Domizi, Sydney Gordon, Yong-hun Kim, Garry Nolan, Paola Betancur, Gerlinde Wernig
Format: Article
Language:English
Published: Nature Portfolio 2020-06-01
Series:Nature Communications
Online Access:https://doi.org/10.1038/s41467-020-16466-4
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author Lu Cui
Shih-Yu Chen
Tristan Lerbs
Jin-Wook Lee
Pablo Domizi
Sydney Gordon
Yong-hun Kim
Garry Nolan
Paola Betancur
Gerlinde Wernig
author_facet Lu Cui
Shih-Yu Chen
Tristan Lerbs
Jin-Wook Lee
Pablo Domizi
Sydney Gordon
Yong-hun Kim
Garry Nolan
Paola Betancur
Gerlinde Wernig
author_sort Lu Cui
collection DOAJ
description Fibroblast contributions to lung fibrosis and in particular their crosstalk with immune cells in the lung are incompletely understood. Here, the authors show an overall immune suppressive environment transcriptionally controlled and maintained by fibroblasts in lung fibrosis with possible therapeutic implications.
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spelling doaj.art-c31003c7ba9446ada3f7ab8183096f6b2022-12-21T21:52:29ZengNature PortfolioNature Communications2041-17232020-06-0111111410.1038/s41467-020-16466-4Activation of JUN in fibroblasts promotes pro-fibrotic programme and modulates protective immunityLu Cui0Shih-Yu Chen1Tristan Lerbs2Jin-Wook Lee3Pablo Domizi4Sydney Gordon5Yong-hun Kim6Garry Nolan7Paola Betancur8Gerlinde Wernig9Department of Pathology, Institute of Stem Cell Biology and Regenerative Medicine (ISCBRM), Stanford University School of MedicineInstitute of Biomedical Sciences, Academia SinicaDepartment of Pathology, Institute of Stem Cell Biology and Regenerative Medicine (ISCBRM), Stanford University School of MedicineDepartment of Genetics, Stanford University School of MedicineDepartment of Pathology, Institute of Stem Cell Biology and Regenerative Medicine (ISCBRM), Stanford University School of MedicineOrca BiosystemsDepartment of Pathology, Institute of Stem Cell Biology and Regenerative Medicine (ISCBRM), Stanford University School of MedicineBaxter Laboratories Department of Microbiology and Immunology, Stanford University School of MedicineDepartment of Radiation Oncology, University of CaliforniaDepartment of Pathology, Institute of Stem Cell Biology and Regenerative Medicine (ISCBRM), Stanford University School of MedicineFibroblast contributions to lung fibrosis and in particular their crosstalk with immune cells in the lung are incompletely understood. Here, the authors show an overall immune suppressive environment transcriptionally controlled and maintained by fibroblasts in lung fibrosis with possible therapeutic implications.https://doi.org/10.1038/s41467-020-16466-4
spellingShingle Lu Cui
Shih-Yu Chen
Tristan Lerbs
Jin-Wook Lee
Pablo Domizi
Sydney Gordon
Yong-hun Kim
Garry Nolan
Paola Betancur
Gerlinde Wernig
Activation of JUN in fibroblasts promotes pro-fibrotic programme and modulates protective immunity
Nature Communications
title Activation of JUN in fibroblasts promotes pro-fibrotic programme and modulates protective immunity
title_full Activation of JUN in fibroblasts promotes pro-fibrotic programme and modulates protective immunity
title_fullStr Activation of JUN in fibroblasts promotes pro-fibrotic programme and modulates protective immunity
title_full_unstemmed Activation of JUN in fibroblasts promotes pro-fibrotic programme and modulates protective immunity
title_short Activation of JUN in fibroblasts promotes pro-fibrotic programme and modulates protective immunity
title_sort activation of jun in fibroblasts promotes pro fibrotic programme and modulates protective immunity
url https://doi.org/10.1038/s41467-020-16466-4
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