Brg1 promotes liver regeneration after partial hepatectomy via regulation of cell cycle

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作者
Baocai Wang
Benedikt Kaufmann
Thomas Engleitner
Miao Lu
Carolin Mogler
Victor Olsavszky
Rupert Öllinger
Suyang Zhong
Cyrill Geraud
Zhangjun Cheng
Roland R. Rad
Roland M. Schmid
Helmut Friess
Norbert Hüser
Daniel Hartmann
Guido von Figura
机构
[1] Technical University of Munich,Department of Surgery, TUM School of Medicine, Klinikum rechts der Isar
[2] Southeast University,Department of General Surgery, the Affiliated Zhongda Hospital, School of Medicine
[3] Technical University of Munich,Institute of Molecular Oncology and Functional Genomics, Department of Medicine II and TranslaTUM Cancer Center, Klinikum rechts der Isar
[4] Technical University of Munich,Institute of Pathology, TUM School of Medicine, Klinikum rechts der Isar
[5] Heidelberg University and Center of Excellence in Dermatology,Department of Dermatology, Venereology, and Allergology, University Medical Center and Medical Faculty Mannheim
[6] Technical University of Munich,Department of Medicine II, TUM School of Medicine, Klinikum rechts der Isar
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摘要
Brahma-related gene 1 (Brg1), a catalytic subunit of the SWItch/Sucrose Non-Fermentable (SWI/SNF) complex, is known to be involved in proliferative cell processes. Liver regeneration is initiated spontaneously after injury and leads to a strong proliferative response. In this study, a hepatocyte-specific Brg1 gene knockout mouse model was used to analyse the role of Brg1 in liver regeneration by performing a 70% partial hepatectomy (PH). After PH, Brg1 was significantly upregulated in wildtype mice. Mice with hepatocyte-specific Brg1 gene knockout showed a significantly lower liver to body weight ratio 48 h post-PH concomitant with a lower hepatocellular proliferation rate compared to wildtype mice. RNA sequencing demonstrated that Brg1 controlled hepatocyte proliferation through the regulation of the p53 pathway and several cell cycle genes. The data of this study reveal a crucial role of Brg1 for liver regeneration by promoting hepatocellular proliferation through modulation of cell cycle genes and, thus, identify Brg1 as potential target for therapeutic approaches.
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