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EBioMedicine. 2019 Sep 12. pii: S2352-3964(19)30611-5. doi: 10.1016/j.ebiom.2019.09.013. [Epub ahead of print]

Knockdown of vimentin reduces mesenchymal phenotype of cholangiocytes in the Mdr2-/- mouse model of primary sclerosing cholangitis (PSC).

Author information

1
Department of Medical Physiology, College of Medicine, Texas A&M University, Bryan, TX, United States of America.
2
Gastroenterology, Medicine, Indiana University, Indianapolis, IN, United States of America.
3
Richard L. Roudebush VA Medical Center, Indianapolis, IN, United States of America; Gastroenterology, Medicine, Indiana University, Indianapolis, IN, United States of America.
4
Department of Nutrition and Food Science, College of Medicine, Texas A&M University, United States of America.
5
University of Tor Vergata, Rome, Italy.
6
Department of Surgery, Indiana University, Indianapolis, IN, United States of America.
7
Department of Pathology, Indiana University, Indianapolis, IN, United States of America.
8
Department of Pathology, Microbiology and Immunology, Vanderbilt University School of Medicine, Nashville, TN, United States of America.
9
Richard L. Roudebush VA Medical Center, Indianapolis, IN, United States of America; Gastroenterology, Medicine, Indiana University, Indianapolis, IN, United States of America. Electronic address: galpini@iu.edu.
10
Department of Medical Physiology, College of Medicine, Texas A&M University, Bryan, TX, United States of America. Electronic address: sglaser@tamu.edu.

Abstract

BACKGROUND:

Cholangiocytes are the target cells of cholangiopathies including primary sclerosing cholangitis (PSC). Vimentin is an intermediate filament protein that has been found in various types of mesenchymal cells. The aim of this study is to evaluate the role of vimentin in the progression of biliary damage/liver fibrosis and whether there is a mesenchymal phenotype of cholangiocytes in the Mdr2-/- model of PSC.

METHODS:

In vivo studies were performed in 12 wk. Mdr2-/- male mice with or without vimentin Vivo-Morpholino treatment and their corresponding control groups. Liver specimens from human PSC patients, human intrahepatic biliary epithelial cells (HIBEpiC) and human hepatic stellate cell lines (HHSteCs) were used to measure changes in epithelial-to-mesenchymal transition (EMT).

FINDINGS:

There was increased mesenchymal phenotype of cholangiocytes in Mdr2-/- mice, which was reduced by treatment of vimentin Vivo-Morpholino. Concomitant with reduced vimentin expression, there was decreased liver damage, ductular reaction, biliary senescence, liver fibrosis and TGF-β1 secretion in Mdr2-/- mice treated with vimentin Vivo-Morpholino. Human PSC patients and derived cell lines had increased expression of vimentin and other mesenchymal markers compared to healthy controls and HIBEpiC, respectively. In vitro silencing of vimentin in HIBEpiC suppressed TGF-β1-induced EMT and fibrotic reaction. HHSteCs had decreased fibrotic reaction and increased cellular senescence after stimulation with cholangiocyte supernatant with reduced vimentin levels.

INTERPRETATION:

Our study demonstrated that knockdown of vimentin reduces mesenchymal phenotype of cholangiocytes, which leads to decreased biliary senescence and liver fibrosis. Inhibition of vimentin may be a key therapeutic target in the treatment of cholangiopathies including PSC. FUND: National Institutes of Health (NIH) awards, VA Merit awards.

KEYWORDS:

Ductular reaction; Fibroblast; Fibrosis; Senescence; Transforming growth factor beta 1

PMID:
31522982
DOI:
10.1016/j.ebiom.2019.09.013
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