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TGF-β1/p65/MAT2A pathway regulates liver fibrogenesis via intracellular SAM
BACKGROUND: Hepatic stellate cell (HSC) activation induced by transforming growth factor β1 (TGF-β1) plays a pivotal role in fibrogenesis, while the complex downstream mediators of TGF-β1 in such process are largely unknown. METHODS: We performed pharmacoproteomic profiling of the mice liver tissues...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6491716/ https://www.ncbi.nlm.nih.gov/pubmed/30926424 http://dx.doi.org/10.1016/j.ebiom.2019.03.058 |
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author | Wang, Kuifeng Fang, Shanhua Liu, Qian Gao, Jing Wang, Xiaoning Zhu, Hongwen Zhu, Zhenyun Ji, Feihong Wu, Jiasheng Ma, Yueming Hu, Lihong Shen, Xu Gao, Daming Zhu, Jiansheng Liu, Ping Zhou, Hu |
author_facet | Wang, Kuifeng Fang, Shanhua Liu, Qian Gao, Jing Wang, Xiaoning Zhu, Hongwen Zhu, Zhenyun Ji, Feihong Wu, Jiasheng Ma, Yueming Hu, Lihong Shen, Xu Gao, Daming Zhu, Jiansheng Liu, Ping Zhou, Hu |
author_sort | Wang, Kuifeng |
collection | PubMed |
description | BACKGROUND: Hepatic stellate cell (HSC) activation induced by transforming growth factor β1 (TGF-β1) plays a pivotal role in fibrogenesis, while the complex downstream mediators of TGF-β1 in such process are largely unknown. METHODS: We performed pharmacoproteomic profiling of the mice liver tissues from control, carbon tetrachloride (CCl(4))-induced fibrosis and NPLC0393 administrated groups. The target gene MAT2A was overexpressed or knocked down in vivo by tail vein injection of AAV vectors. We examined NF-κB transcriptional activity on MAT2A promoter via luciferase assay. Intracellular SAM contents were analyzed by LC-MS method. FINDINGS: We found that methionine adenosyltransferase 2A (MAT2A) is significantly upregulated in the CCl(4)-induced fibrosis mice, and application of NPLC0393, a known small molecule inhibitor of TGF-β1 signaling pathway, inhibits the upregulation of MAT2A. Mechanistically, TGF-β1 induces phosphorylation of p65, i.e., activation of NF-κB, thereby promoting mRNA transcription and protein expression of MAT2A and reduces S-adenosylmethionine (SAM) concentration in HSCs. Consistently, in vivo and in vitro knockdown of MAT2A alleviates CCl(4)- and TGF-β1-induced HSC activation, whereas in vivo overexpression of MAT2A facilitates hepatic fibrosis and abolishes therapeutic effect of NPLC0393. INTERPRETATION: This study identifies TGF-β1/p65/MAT2A pathway that is involved in the regulation of intracellular SAM concentration and liver fibrogenesis, suggesting that this pathway is a potential therapeutic target for hepatic fibrosis. FUND: This work was supported by National Natural Science Foundation of China (No. 81500469, 81573873, 81774196 and 31800693), Zhejiang Provincial Natural Science Foundation of China (No. Y15H030004), the National Key Research and Development Program from the Ministry of Science and Technology of China (No. 2017YFC1700200) and the Key Program of National Natural Science Foundation of China (No. 8153000502). |
format | Online Article Text |
id | pubmed-6491716 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-64917162019-05-06 TGF-β1/p65/MAT2A pathway regulates liver fibrogenesis via intracellular SAM Wang, Kuifeng Fang, Shanhua Liu, Qian Gao, Jing Wang, Xiaoning Zhu, Hongwen Zhu, Zhenyun Ji, Feihong Wu, Jiasheng Ma, Yueming Hu, Lihong Shen, Xu Gao, Daming Zhu, Jiansheng Liu, Ping Zhou, Hu EBioMedicine Research paper BACKGROUND: Hepatic stellate cell (HSC) activation induced by transforming growth factor β1 (TGF-β1) plays a pivotal role in fibrogenesis, while the complex downstream mediators of TGF-β1 in such process are largely unknown. METHODS: We performed pharmacoproteomic profiling of the mice liver tissues from control, carbon tetrachloride (CCl(4))-induced fibrosis and NPLC0393 administrated groups. The target gene MAT2A was overexpressed or knocked down in vivo by tail vein injection of AAV vectors. We examined NF-κB transcriptional activity on MAT2A promoter via luciferase assay. Intracellular SAM contents were analyzed by LC-MS method. FINDINGS: We found that methionine adenosyltransferase 2A (MAT2A) is significantly upregulated in the CCl(4)-induced fibrosis mice, and application of NPLC0393, a known small molecule inhibitor of TGF-β1 signaling pathway, inhibits the upregulation of MAT2A. Mechanistically, TGF-β1 induces phosphorylation of p65, i.e., activation of NF-κB, thereby promoting mRNA transcription and protein expression of MAT2A and reduces S-adenosylmethionine (SAM) concentration in HSCs. Consistently, in vivo and in vitro knockdown of MAT2A alleviates CCl(4)- and TGF-β1-induced HSC activation, whereas in vivo overexpression of MAT2A facilitates hepatic fibrosis and abolishes therapeutic effect of NPLC0393. INTERPRETATION: This study identifies TGF-β1/p65/MAT2A pathway that is involved in the regulation of intracellular SAM concentration and liver fibrogenesis, suggesting that this pathway is a potential therapeutic target for hepatic fibrosis. FUND: This work was supported by National Natural Science Foundation of China (No. 81500469, 81573873, 81774196 and 31800693), Zhejiang Provincial Natural Science Foundation of China (No. Y15H030004), the National Key Research and Development Program from the Ministry of Science and Technology of China (No. 2017YFC1700200) and the Key Program of National Natural Science Foundation of China (No. 8153000502). Elsevier 2019-03-27 /pmc/articles/PMC6491716/ /pubmed/30926424 http://dx.doi.org/10.1016/j.ebiom.2019.03.058 Text en © 2019 The Authors. Published by Elsevier B.V. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Research paper Wang, Kuifeng Fang, Shanhua Liu, Qian Gao, Jing Wang, Xiaoning Zhu, Hongwen Zhu, Zhenyun Ji, Feihong Wu, Jiasheng Ma, Yueming Hu, Lihong Shen, Xu Gao, Daming Zhu, Jiansheng Liu, Ping Zhou, Hu TGF-β1/p65/MAT2A pathway regulates liver fibrogenesis via intracellular SAM |
title | TGF-β1/p65/MAT2A pathway regulates liver fibrogenesis via intracellular SAM |
title_full | TGF-β1/p65/MAT2A pathway regulates liver fibrogenesis via intracellular SAM |
title_fullStr | TGF-β1/p65/MAT2A pathway regulates liver fibrogenesis via intracellular SAM |
title_full_unstemmed | TGF-β1/p65/MAT2A pathway regulates liver fibrogenesis via intracellular SAM |
title_short | TGF-β1/p65/MAT2A pathway regulates liver fibrogenesis via intracellular SAM |
title_sort | tgf-β1/p65/mat2a pathway regulates liver fibrogenesis via intracellular sam |
topic | Research paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6491716/ https://www.ncbi.nlm.nih.gov/pubmed/30926424 http://dx.doi.org/10.1016/j.ebiom.2019.03.058 |
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