| Literature DB >> 33792165 |
Joaquim Javary1,2, Nathalie Allain1,2, Zakaria Ezzoukhry1,2, Sylvaine Di Tommaso1,2,3, Jean-William Dupuy4, Pierre Costet5, Nathalie Dugot-Senant6, Frédéric Saltel1,2, Violaine Moreau1,2, Pierre Dubus1,2,7, Samira Benhamouche-Trouillet1,2.
Abstract
Previous studies have shown that Reptin is overexpressed in hepatocellular carcinoma and that it is necessary for in vitro proliferation and cell survival. However, its pathophysiological role in vivo remains unknown. We aimed to study the role of Reptin in hepatocyte proliferation after regeneration using a liver Reptin knock-out model (ReptinLKO ). Interestingly, hepatocyte proliferation is strongly impaired in ReptinLKO mice 36 h after partial hepatectomy, associated with a decrease of cyclin-A expression and mTORC1 and MAPK signalling, leading to an impaired liver regeneration. Moreover, in the ReptinLKO model, we have observed a progressive loss of Reptin invalidation associated with an atypical liver regeneration. Hypertrophic and proliferative hepatocytes gradually replace ReptinKO hypotrophic hepatocytes. To conclude, our results show that Reptin is required for hepatocyte proliferation in vivo and liver regeneration and that it plays a crucial role in hepatocyte survival and liver homeostasis.Entities:
Keywords: RUVBL2; hepatectomy; hepatocyte proliferation; hypertrophic; liver regeneration; reptin
Year: 2021 PMID: 33792165 DOI: 10.1111/liv.14886
Source DB: PubMed Journal: Liver Int ISSN: 1478-3223 Impact factor: 5.828