Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
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
_version_ 1783414998621487104
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
work_keys_str_mv AT wangkuifeng tgfb1p65mat2apathwayregulatesliverfibrogenesisviaintracellularsam
AT fangshanhua tgfb1p65mat2apathwayregulatesliverfibrogenesisviaintracellularsam
AT liuqian tgfb1p65mat2apathwayregulatesliverfibrogenesisviaintracellularsam
AT gaojing tgfb1p65mat2apathwayregulatesliverfibrogenesisviaintracellularsam
AT wangxiaoning tgfb1p65mat2apathwayregulatesliverfibrogenesisviaintracellularsam
AT zhuhongwen tgfb1p65mat2apathwayregulatesliverfibrogenesisviaintracellularsam
AT zhuzhenyun tgfb1p65mat2apathwayregulatesliverfibrogenesisviaintracellularsam
AT jifeihong tgfb1p65mat2apathwayregulatesliverfibrogenesisviaintracellularsam
AT wujiasheng tgfb1p65mat2apathwayregulatesliverfibrogenesisviaintracellularsam
AT mayueming tgfb1p65mat2apathwayregulatesliverfibrogenesisviaintracellularsam
AT hulihong tgfb1p65mat2apathwayregulatesliverfibrogenesisviaintracellularsam
AT shenxu tgfb1p65mat2apathwayregulatesliverfibrogenesisviaintracellularsam
AT gaodaming tgfb1p65mat2apathwayregulatesliverfibrogenesisviaintracellularsam
AT zhujiansheng tgfb1p65mat2apathwayregulatesliverfibrogenesisviaintracellularsam
AT liuping tgfb1p65mat2apathwayregulatesliverfibrogenesisviaintracellularsam
AT zhouhu tgfb1p65mat2apathwayregulatesliverfibrogenesisviaintracellularsam