{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Jiang B"],"funding":["National Natural Science Foundation of China","National Natural Science Foundation of China (National Science Foundation of China)"],"pagination":["204"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC9012830"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["8(1)"],"pubmed_abstract":["Iroquois homeobox transcription factor 5 (IRX5) plays a pivotal role in extramedullary adipogenesis, but little is known about the effects of IRX5 on adipogenesis of human bone marrow-derived mesenchymal stem cells (hMSCs). In this study, we aimed to determine the effect of IRX5 on hMSCs adipogenesis. By means of qPCR analysis, we determined that IRX5 expression was elevated during adipogenic commitment of hMSCs. The biologic role of IRX5 was further investigated by employing a gain/loss-of-function strategy using an in vitro lentivirus-based system. IRX5 overexpression promoted adipogenesis whereas IRX5 knockdown reduced the adipogenic phenotype. RNA-seq and metabolomics revealed that IRX5 overexpression repressed glycolysis. Dual-luciferase assay results showed that IRX5 overexpression t"],"journal":["Cell death discovery"],"pubmed_title":["IRX5 promotes adipogenesis of hMSCs by repressing glycolysis."],"pmcid":["PMC9012830"],"funding_grant_id":["81970918","81800945"],"pubmed_authors":["Huang C","Jiang B","Tian T","Song F","Huang L","Marmo T","Yao H","Wu H"],"additional_accession":[]},"is_claimable":false,"name":"IRX5 promotes adipogenesis of hMSCs by repressing glycolysis.","description":"Iroquois homeobox transcription factor 5 (IRX5) plays a pivotal role in extramedullary adipogenesis, but little is known about the effects of IRX5 on adipogenesis of human bone marrow-derived mesenchymal stem cells (hMSCs). In this study, we aimed to determine the effect of IRX5 on hMSCs adipogenesis. By means of qPCR analysis, we determined that IRX5 expression was elevated during adipogenic commitment of hMSCs. The biologic role of IRX5 was further investigated by employing a gain/loss-of-function strategy using an in vitro lentivirus-based system. IRX5 overexpression promoted adipogenesis whereas IRX5 knockdown reduced the adipogenic phenotype. RNA-seq and metabolomics revealed that IRX5 overexpression repressed glycolysis. Dual-luciferase assay results showed that IRX5 overexpression t","dates":{"release":"2022-01-01T00:00:00Z","publication":"2022 Apr","modification":"2025-04-05T22:17:16.042Z","creation":"2025-02-19T04:04:58.935Z"},"accession":"S-EPMC9012830","cross_references":{"pubmed":["35428362"],"doi":["10.1038/s41420-022-00986-7"]}}