{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Tsuzuki S"],"funding":["Grants-in-Aid for Scientific Research","Grants-in-Aid for Scientific Research (KAKENHI)","Japan Agency for Medical Research and Development"],"pagination":["7075"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC10138705"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["24(8)"],"pubmed_abstract":["Human iPSC-derived liver organoids (LO) or hepatic spheroids (HS) have attracted widespread interest, and the numerous studies on them have recently provided various production protocols. However, the mechanism by which the 3D structures of LO and HS are formed from the 2D-cultured cells and the mechanism of the LO and HS maturation remain largely unknown. In this study, we demonstrate that <i>PDGFRA</i> is specifically induced in the cells that are suitable for HS formation and that PDGF receptors and signaling are required for HS formation and maturation. Additionally, in vivo, we show that the localization of PDGFRα is in complete agreement with mouse E9.5 hepatoblasts, which begin to form the 3D-structural liver bud from the single layer. Our results present that <i>PDGFRA</i> play imp"],"journal":["International journal of molecular sciences"],"pubmed_title":["PDGF Receptors and Signaling Are Required for 3D-Structure Formation and Differentiation of Human iPSC-Derived Hepatic Spheroids."],"pmcid":["PMC10138705"],"funding_grant_id":["20K08952","22bm0304002h0310","22bm1004003h0003","21fk0310103h0505","22fk0210073s0503","21H04830","22bk0104102h0003","19lm0203005h9903","18KK0252"],"pubmed_authors":["Kasai T","Tsuzuki S","Ueno Y","Yamaguchi T","Taniguchi H","Okumura T"],"additional_accession":[]},"is_claimable":false,"name":"PDGF Receptors and Signaling Are Required for 3D-Structure Formation and Differentiation of Human iPSC-Derived Hepatic Spheroids.","description":"Human iPSC-derived liver organoids (LO) or hepatic spheroids (HS) have attracted widespread interest, and the numerous studies on them have recently provided various production protocols. However, the mechanism by which the 3D structures of LO and HS are formed from the 2D-cultured cells and the mechanism of the LO and HS maturation remain largely unknown. In this study, we demonstrate that <i>PDGFRA</i> is specifically induced in the cells that are suitable for HS formation and that PDGF receptors and signaling are required for HS formation and maturation. Additionally, in vivo, we show that the localization of PDGFRα is in complete agreement with mouse E9.5 hepatoblasts, which begin to form the 3D-structural liver bud from the single layer. Our results present that <i>PDGFRA</i> play imp","dates":{"release":"2023-01-01T00:00:00Z","publication":"2023 Apr","modification":"2026-06-23T03:26:37.58Z","creation":"2025-02-19T04:45:44.296Z"},"accession":"S-EPMC10138705","cross_references":{"pubmed":["37108241"],"doi":["10.3390/ijms24087075"]}}