| First Author | Kim JY | Year | 2022 |
| Journal | Am J Physiol Endocrinol Metab | Volume | 322 |
| Issue | 2 | Pages | E118-E131 |
| PubMed ID | 34894722 | Mgi Jnum | J:331169 |
| Mgi Id | MGI:7256532 | Doi | 10.1152/ajpendo.00309.2021 |
| Citation | Kim JY, et al. (2022) RORalpha contributes to the maintenance of genome ploidy in the liver of mice with diet-induced nonalcoholic steatohepatitis. Am J Physiol Endocrinol Metab 322(2):E118-E131 |
| abstractText | Hepatic polyploidization is closely linked to the progression of nonalcoholic fatty liver disease (NAFLD); however, the underlying molecular mechanism is not clearly understood. In this study, we demonstrated the role of retinoic acid-related orphan receptor alpha (RORalpha) in the maintenance of genomic integrity, particularly in the pathogenesis of NAFLD, using the high-fat diet (HFD)-fed liver-specific RORalpha knockout (RORalpha-LKO) mouse model. First, we observed that the loss of hepatic retinoic acid receptor-related orphan receptor alpha (RORalpha) accelerated hepatocyte nuclear polyploidization after HFD feeding. In 70% partial hepatectomy experiments, enrichment of hepatocyte polyploidy was more obvious in the RORalpha-LKO animals, which was accompanied by early progression to the S phase and blockade of the G2/M transition, suggesting a potential role of RORalpha in suppressing hepatocyte polyploidization in the regenerating liver. An analysis of a publicly available RNA sequencing (RNA-seq) and chromatin immunoprecipitation-seq dataset, together with the Search Tool of the Retrieval of Interacting Genes/Proteins database resource, revealed that DNA endoreplication was the top-enriched biological process Gene Ontology term. Furthermore, we found that E2f7 and E2f8, which encode key transcription factors for DNA endoreplication, were the downstream targets of RORalpha-induced transcriptional repression. Finally, we showed that the administration of JC1-40, an RORalpha activator (5 mg/kg body wt), significantly reduced hepatic nuclear polyploidization in the HFD-fed mice. Together, our observations suggest that the RORalpha-induced suppression of hepatic polyploidization may provide new insights into the pathological polyploidy of NAFLD and may contribute to the development of therapeutic strategies for the treatment of NAFLD.NEW & NOTEWORTHY It has been reported that hepatic polyploidization is closely linked to the progression of NAFLD. Here, we showed that the genetic depletion of hepatic RORalpha in mice accelerated hepatocyte polyploidization after high-fat diet feeding. The mechanism could be the RORalpha-mediated repression of E2f7 and E2f8, key transcription factors for DNA endoreplication. Thus, preservation of genome integrity by RORalpha could provide a new insight for developing therapeutics against the disease. |
