Z Gastroenterol 2021; 59(01): e12-e13
DOI: 10.1055/s-0040-1721975
Poster Visit Session I Basic Hepatology (Fibrogenesis, NPC, Transport)
Friday, January 29, 2021, 12:30 pm – 1:15 pm, Poster Session Virtual Venue

Hepatocellular Brg1 promotes CCl4-induced liver inflammation, ECM accumulation and fibrosis in mice

D Hartmann
1   Klinikum rechts der Isar, Technische Universität München, Klinik und Poliklinik für Chirurgie, München, Germany
,
B Wang
1   Klinikum rechts der Isar, Technische Universität München, Klinik und Poliklinik für Chirurgie, München, Germany
2   Department of General Surgery, Affiliated Zhongda Hospital, Southeast University, Nanjing, China
,
B Kaufmann
1   Klinikum rechts der Isar, Technische Universität München, Klinik und Poliklinik für Chirurgie, München, Germany
,
Y Yin
1   Klinikum rechts der Isar, Technische Universität München, Klinik und Poliklinik für Chirurgie, München, Germany
,
M Steffani
1   Klinikum rechts der Isar, Technische Universität München, Klinik und Poliklinik für Chirurgie, München, Germany
,
C Mogler
3   Klinikum rechts der Isar, Technische Universität, Pathologisches Institut, München, Germany
,
Z Cheng
2   Department of General Surgery, Affiliated Zhongda Hospital, Southeast University, Nanjing, China
,
N Hüser
1   Klinikum rechts der Isar, Technische Universität München, Klinik und Poliklinik für Chirurgie, München, Germany
,
G von Figura
4   Klinikum rechts der Isar, Technische Universität, II. Medizinische Klinik, München, Germany
,
H Friess
1   Klinikum rechts der Isar, Technische Universität München, Klinik und Poliklinik für Chirurgie, München, Germany
› Author Affiliations
 
 

    Questions Brahma-related gene 1 (Brg1) is a catalytic subunit of the SWItch/Sucrose Non-Fermentable (SWI/SNF) complex and has recently been identified as important for liver regeneration. Liver fibrosis is a progressive pathological process that involves the depletion of the hepatocellular regenerative capacity and ultimately leads to the development of liver cirrhosis and even hepatocellular carcinoma. So far the role of Brg1 in liver fibrosis is unclear.

    Methods In this study, we examined the effect of Brg1 on the development of liver fibrosis. Hepatocyte specific Brg1 knockout mice (AlbCre Brg1fl/fl) were injected with carbon tetrachloride (CCl4) to induce liver fibrosis. Brg1 expression was determined by Western blot and liver fibrosis was assessed by liver-to-body weight ratio analysis, serum ALT ELISA, Sirius red staining, and alpha-smooth muscle actin (a-SMA) staining.

    Results Brg1 expression was significantly increased in the fibrotic liver tissue of wild-type mice compared to untreated wild-type mice. The livers of the Brg1 knockout animals showed a significantly reduced liver inflammation, extracellular matrix accumulation and liver fibrosis compared to wild-type mice. Furthermore, we were able to show that HSC activation and inflammatory response during CCl4-induced liver fibrosis are associated with Brg1, which mediates the TNF-α/NF-kB pathway.

    Conclusions These results highlight a new aspect of Brg1 in the pathogenesis of liver fibrosis. We have shown that hepatocyte-specific Brg1 deletion prevents liver fibrosis in CCl4-treated mice. In conclusion, Brg1 promotes the progression of liver fibrosis in mice and therefore can be used as a potential therapeutic target for the treatment of patients with liver fibrosis due to chronic injury.

    Correlation of tgfb2 mRNA expression to disease prog


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    Publication History

    Article published online:
    04 January 2021

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