PTP4A1 promotes TGFβ signaling and fibrosis in systemic sclerosis

Although protein tyrosine kinases are being explored as antifibrotic agents for the treatment of systemic sclerosis, little is known about the function of counteractive protein tyrosine phosphatases in this context. Here, the authors show that PTP4A1 is highly expressed by fibroblasts from patients...

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Autores principales: Cristiano Sacchetti, Yunpeng Bai, Stephanie M. Stanford, Paola Di Benedetto, Paola Cipriani, Eugenio Santelli, Sonsoles Piera-Velazquez, Vladimir Chernitskiy, William B. Kiosses, Arnold Ceponis, Klaus H. Kaestner, Francesco Boin, Sergio A. Jimenez, Roberto Giacomelli, Zhong-Yin Zhang, Nunzio Bottini
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Publicado: Nature Portfolio 2017
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Acceso en línea:https://doaj.org/article/bda2249f57354c398a9b7c97bc41a7fd
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spelling oai:doaj.org-article:bda2249f57354c398a9b7c97bc41a7fd2021-12-02T14:42:01ZPTP4A1 promotes TGFβ signaling and fibrosis in systemic sclerosis10.1038/s41467-017-01168-12041-1723https://doaj.org/article/bda2249f57354c398a9b7c97bc41a7fd2017-10-01T00:00:00Zhttps://doi.org/10.1038/s41467-017-01168-1https://doaj.org/toc/2041-1723Although protein tyrosine kinases are being explored as antifibrotic agents for the treatment of systemic sclerosis, little is known about the function of counteractive protein tyrosine phosphatases in this context. Here, the authors show that PTP4A1 is highly expressed by fibroblasts from patients with systemic sclerosis and promotes TGFβ activity via SRC–ERK–SMAD3 signaling.Cristiano SacchettiYunpeng BaiStephanie M. StanfordPaola Di BenedettoPaola CiprianiEugenio SantelliSonsoles Piera-VelazquezVladimir ChernitskiyWilliam B. KiossesArnold CeponisKlaus H. KaestnerFrancesco BoinSergio A. JimenezRoberto GiacomelliZhong-Yin ZhangNunzio BottiniNature PortfolioarticleScienceQENNature Communications, Vol 8, Iss 1, Pp 1-14 (2017)
institution DOAJ
collection DOAJ
language EN
topic Science
Q
spellingShingle Science
Q
Cristiano Sacchetti
Yunpeng Bai
Stephanie M. Stanford
Paola Di Benedetto
Paola Cipriani
Eugenio Santelli
Sonsoles Piera-Velazquez
Vladimir Chernitskiy
William B. Kiosses
Arnold Ceponis
Klaus H. Kaestner
Francesco Boin
Sergio A. Jimenez
Roberto Giacomelli
Zhong-Yin Zhang
Nunzio Bottini
PTP4A1 promotes TGFβ signaling and fibrosis in systemic sclerosis
description Although protein tyrosine kinases are being explored as antifibrotic agents for the treatment of systemic sclerosis, little is known about the function of counteractive protein tyrosine phosphatases in this context. Here, the authors show that PTP4A1 is highly expressed by fibroblasts from patients with systemic sclerosis and promotes TGFβ activity via SRC–ERK–SMAD3 signaling.
format article
author Cristiano Sacchetti
Yunpeng Bai
Stephanie M. Stanford
Paola Di Benedetto
Paola Cipriani
Eugenio Santelli
Sonsoles Piera-Velazquez
Vladimir Chernitskiy
William B. Kiosses
Arnold Ceponis
Klaus H. Kaestner
Francesco Boin
Sergio A. Jimenez
Roberto Giacomelli
Zhong-Yin Zhang
Nunzio Bottini
author_facet Cristiano Sacchetti
Yunpeng Bai
Stephanie M. Stanford
Paola Di Benedetto
Paola Cipriani
Eugenio Santelli
Sonsoles Piera-Velazquez
Vladimir Chernitskiy
William B. Kiosses
Arnold Ceponis
Klaus H. Kaestner
Francesco Boin
Sergio A. Jimenez
Roberto Giacomelli
Zhong-Yin Zhang
Nunzio Bottini
author_sort Cristiano Sacchetti
title PTP4A1 promotes TGFβ signaling and fibrosis in systemic sclerosis
title_short PTP4A1 promotes TGFβ signaling and fibrosis in systemic sclerosis
title_full PTP4A1 promotes TGFβ signaling and fibrosis in systemic sclerosis
title_fullStr PTP4A1 promotes TGFβ signaling and fibrosis in systemic sclerosis
title_full_unstemmed PTP4A1 promotes TGFβ signaling and fibrosis in systemic sclerosis
title_sort ptp4a1 promotes tgfβ signaling and fibrosis in systemic sclerosis
publisher Nature Portfolio
publishDate 2017
url https://doaj.org/article/bda2249f57354c398a9b7c97bc41a7fd
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