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Brg1 promotes liver regeneration after partial hepatectomy via regulation of cell cycle
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-spe...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6382836/ https://www.ncbi.nlm.nih.gov/pubmed/30787318 http://dx.doi.org/10.1038/s41598-019-38568-w |
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author | Wang, Baocai Kaufmann, Benedikt Engleitner, Thomas Lu, Miao Mogler, Carolin Olsavszky, Victor Öllinger, Rupert Zhong, Suyang Geraud, Cyrill Cheng, Zhangjun Rad, Roland R. Schmid, Roland M. Friess, Helmut Hüser, Norbert Hartmann, Daniel von Figura, Guido |
author_facet | Wang, Baocai Kaufmann, Benedikt Engleitner, Thomas Lu, Miao Mogler, Carolin Olsavszky, Victor Öllinger, Rupert Zhong, Suyang Geraud, Cyrill Cheng, Zhangjun Rad, Roland R. Schmid, Roland M. Friess, Helmut Hüser, Norbert Hartmann, Daniel von Figura, Guido |
author_sort | Wang, Baocai |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-6382836 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-63828362019-02-25 Brg1 promotes liver regeneration after partial hepatectomy via regulation of cell cycle Wang, Baocai Kaufmann, Benedikt Engleitner, Thomas Lu, Miao Mogler, Carolin Olsavszky, Victor Öllinger, Rupert Zhong, Suyang Geraud, Cyrill Cheng, Zhangjun Rad, Roland R. Schmid, Roland M. Friess, Helmut Hüser, Norbert Hartmann, Daniel von Figura, Guido Sci Rep Article 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. Nature Publishing Group UK 2019-02-20 /pmc/articles/PMC6382836/ /pubmed/30787318 http://dx.doi.org/10.1038/s41598-019-38568-w Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Wang, Baocai Kaufmann, Benedikt Engleitner, Thomas Lu, Miao Mogler, Carolin Olsavszky, Victor Öllinger, Rupert Zhong, Suyang Geraud, Cyrill Cheng, Zhangjun Rad, Roland R. Schmid, Roland M. Friess, Helmut Hüser, Norbert Hartmann, Daniel von Figura, Guido Brg1 promotes liver regeneration after partial hepatectomy via regulation of cell cycle |
title | Brg1 promotes liver regeneration after partial hepatectomy via regulation of cell cycle |
title_full | Brg1 promotes liver regeneration after partial hepatectomy via regulation of cell cycle |
title_fullStr | Brg1 promotes liver regeneration after partial hepatectomy via regulation of cell cycle |
title_full_unstemmed | Brg1 promotes liver regeneration after partial hepatectomy via regulation of cell cycle |
title_short | Brg1 promotes liver regeneration after partial hepatectomy via regulation of cell cycle |
title_sort | brg1 promotes liver regeneration after partial hepatectomy via regulation of cell cycle |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6382836/ https://www.ncbi.nlm.nih.gov/pubmed/30787318 http://dx.doi.org/10.1038/s41598-019-38568-w |
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