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Now published in The Lancet

Autocrine CTHRC1 Activates Hepatic Stellate Cells and Promotes Liver Fibrosis by Activating TGF-β Signaling

47 Pages Posted: 10 Dec 2018

See all articles by Jun Li

Jun Li

Shanghai Jiao Tong University (SJTU)

Mingze Ma

Shanghai Jiao Tong University (SJTU)

Yahui Wang

Shanghai Jiao Tong University (SJTU)

Shuheng Jiang

Shanghai Jiao Tong University (SJTU)

Xueli Zhang

Shanghai Jiao Tong University (SJTU)

Yanli Zhang

Shanghai Jiao Tong University (SJTU)

Xiaomei Yanga

Shanghai Jiao Tong University (SJTU)

Guangang Tian

Shanghai Jiao Tong University (SJTU)

Qing Li

Shanghai Jiao Tong University (SJTU)

Yang Wang

Shanghai Jiao Tong University (SJTU)

Lei Zhu

Shanghai Jiao Tong University (SJTU)

Huizhen Nie

Shanghai Jiao Tong University (SJTU)

Mingxuan Feng

Shanghai Jiao Tong University (SJTU)

Chunjie Xu

Shanghai Jiao Tong University (SJTU)

Qiang Xia

Shanghai Jiao Tong University (SJTU) - Ren Ji Hospital

Jianren Gu

Fudan University - Shanghai Medical College; Shanghai Jiao Tong University (SJTU) - State Key Laboratory of Oncogenes and Related Genes

Qing Xu

Shanghai Jiao Tong University (SJTU) - Department of Gastrointestinal Surgery

Zhi-gang Zhang

Shanghai Jiao Tong University (SJTU) - School of Chemistry and Chemical Engineering

More...

Abstract

Background: Hepatic fibrosis is caused by chronic liver injury and may progress toward liver cirrhosis, and even hepatocellular carcinoma. However, current treatment is not satisfactory. Therefore, there is a mandate to find novel therapeutic targets to improve therapy, and biomarkers to monitor therapeutic response.  

Methods: Liver fibrosis was induced by carbon tetrachloride (CCl4) or thioacetamide (TAA) in wild type (WT) or CTHRC1-/- mice, followed by immunofluorescence and immunohistochemical analyses. CTHRC1 monoclonal antibody (mAb) was used to abrogate the effect of CTHRC1 in vitro and in vivo.  

Results: Here, we reported that collagen triple helix repeat containing 1 (CTHRC1), a secreted protein derived from hepatic stellate cells (HSCs), was significantly up-regulated in fibrotic liver tissues. CTHRC1 promoted HSCs transformation from a quiescent to an activated state, and enhanced migratory or contractile capacities of HSCs by activating TGF-β signaling. CCl4 or TAA-induced liver fibrosis was attenuated in CTHRC-/- mice compared with littermate control, while a monoclonal antibody of CTHRC1 suppressed liver fibrosis in WT mice treated with CCl4 or TAA. Interpretation: We demonstrated that CTHRC1 is a new regulator of liver fibrosis by modulating TGF-β signaling. Targeting CTHRC1 could be a promising therapeutic approach, which can suppress TGF-β signaling and avoid the side effects caused by directly targeting TGF-β. CTHRC1 could also be a potential biomarker for monitoring response to anti-fibrotic therapy.

Funding Statement: This study was supported by the National Natural Science Foundation of China (ID 81672358, 81871923, 81872242), the Shanghai Municipal Education Commission — Gaofeng Clinical Medicine Grant Support (ID 20181708), the Natural Science Foundation of Shanghai (ID 17ZR1428300), and Shanghai Municipal Health Bureau (ID 2018BR32). The funders did not play a role in manuscript design, data collection, data analysis, interpretation nor writing of the manuscript

Declaration of Interests: The authors have declared that no conflict of interest exists.

Ethics Approval Statement: All of the human materials were obtained with informed content, and protocols were approved by the ethical review committee of the World Health Organization Collaborating Center for Research in Human Production (authorized by the Shanghai Municipal Government).

Mice were housed and manipulated according to protocols approved by the East China Normal University Animal Care Commission. All animals received humane care according to the criteria outlined in the “Guide for the Care and Use of Laboratory Animals” prepared by the National Academy of Sciences and published by the National Institutes of Health.

Keywords: Liver fibrosis; CTHRC1; HSCs; TGF-β signaling

Suggested Citation

Li, Jun and Ma, Mingze and Wang, Yahui and Jiang, Shuheng and Zhang, Xueli and Zhang, Yanli and Yanga, Xiaomei and Tian, Guangang and Li, Qing and Wang, Yang and Zhu, Lei and Nie, Huizhen and Feng, Mingxuan and Xu, Chunjie and Xia, Qiang and Gu, Jianren and Xu, Qing and Zhang, Zhi-gang, Autocrine CTHRC1 Activates Hepatic Stellate Cells and Promotes Liver Fibrosis by Activating TGF-β Signaling (May 12, 2018). Available at SSRN: https://ssrn.com/abstract=3296651 or http://dx.doi.org/10.2139/ssrn.3296651

Jun Li

Shanghai Jiao Tong University (SJTU)

KoGuan Law School
Shanghai 200030, Shanghai 200052
China

Mingze Ma

Shanghai Jiao Tong University (SJTU)

KoGuan Law School
Shanghai 200030, Shanghai 200052
China

Yahui Wang

Shanghai Jiao Tong University (SJTU)

KoGuan Law School
Shanghai 200030, Shanghai 200052
China

Shuheng Jiang

Shanghai Jiao Tong University (SJTU)

KoGuan Law School
Shanghai 200030, Shanghai 200052
China

Xueli Zhang

Shanghai Jiao Tong University (SJTU)

KoGuan Law School
Shanghai 200030, Shanghai 200052
China

Yanli Zhang

Shanghai Jiao Tong University (SJTU)

KoGuan Law School
Shanghai 200030, Shanghai 200052
China

Xiaomei Yanga

Shanghai Jiao Tong University (SJTU)

KoGuan Law School
Shanghai 200030, Shanghai 200052
China

Guangang Tian

Shanghai Jiao Tong University (SJTU)

KoGuan Law School
Shanghai 200030, Shanghai 200052
China

Qing Li

Shanghai Jiao Tong University (SJTU)

KoGuan Law School
Shanghai 200030, Shanghai 200052
China

Yang Wang

Shanghai Jiao Tong University (SJTU)

KoGuan Law School
Shanghai 200030, Shanghai 200052
China

Lei Zhu

Shanghai Jiao Tong University (SJTU)

KoGuan Law School
Shanghai 200030, Shanghai 200052
China

Huizhen Nie

Shanghai Jiao Tong University (SJTU)

KoGuan Law School
Shanghai 200030, Shanghai 200052
China

Mingxuan Feng

Shanghai Jiao Tong University (SJTU)

KoGuan Law School
Shanghai 200030, Shanghai 200052
China

Chunjie Xu

Shanghai Jiao Tong University (SJTU)

KoGuan Law School
Shanghai 200030, Shanghai 200052
China

Qiang Xia

Shanghai Jiao Tong University (SJTU) - Ren Ji Hospital

160 Pujian Road
Shanghai, 200127
China

Jianren Gu

Fudan University - Shanghai Medical College

Shanghai, 200032
China

Shanghai Jiao Tong University (SJTU) - State Key Laboratory of Oncogenes and Related Genes

800 Dongchuan Road
Shanghai, Shanghai 200240
China

Qing Xu

Shanghai Jiao Tong University (SJTU) - Department of Gastrointestinal Surgery ( email )

160 Pujian Road
Shanghai, 200127
China

Zhi-gang Zhang (Contact Author)

Shanghai Jiao Tong University (SJTU) - School of Chemistry and Chemical Engineering ( email )

Shanghai, 200240
China

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