{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Kim JY"],"funding":["Korea Health Industry Development Institute","National Resaerch Foundation of Korea"],"pagination":["469"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC7643360"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["11(1)"],"pubmed_abstract":["<h4>Background</h4>Placenta-derived mesenchymal stem cells (PD-MSCs) have unique immunomodulatory properties. Phosphatase of regenerating liver-1 (PRL-1) regulates the self-renewal ability of stem cells and promotes proliferation. Graves' ophthalmopathy (GO) is an autoimmune inflammatory disease of the orbit and is characterized by increased orbital levels of adipose tissue. Here, we evaluated the therapeutic mechanism for regulation of adipogenesis by PRL-1-overexpressing PD-MSCs (PD-MSCs<sup>PRL-1</sup>, PRL-1+) in orbital fibroblast (OF) with GO patients.<h4>Methods</h4>PD-MSCs isolated from human placenta were transfected with the PRL-1 gene using nonviral transfection method. Primary OFs were isolated from orbital adipose tissue specimens from GO patients. After maturation as adipogen"],"journal":["Stem cell research & therapy"],"pubmed_title":["Functionally enhanced placenta-derived mesenchymal stem cells inhibit adipogenesis in orbital fibroblasts with Graves' ophthalmopathy."],"pmcid":["PMC7643360"],"funding_grant_id":["2019R1l1A1A01057255","HI16C1599"],"pubmed_authors":["Kim GJ","Kim JY","Lew H","Lee HJ","Park S"],"additional_accession":[]},"is_claimable":false,"name":"Functionally enhanced placenta-derived mesenchymal stem cells inhibit adipogenesis in orbital fibroblasts with Graves' ophthalmopathy.","description":"<h4>Background</h4>Placenta-derived mesenchymal stem cells (PD-MSCs) have unique immunomodulatory properties. Phosphatase of regenerating liver-1 (PRL-1) regulates the self-renewal ability of stem cells and promotes proliferation. Graves' ophthalmopathy (GO) is an autoimmune inflammatory disease of the orbit and is characterized by increased orbital levels of adipose tissue. Here, we evaluated the therapeutic mechanism for regulation of adipogenesis by PRL-1-overexpressing PD-MSCs (PD-MSCs<sup>PRL-1</sup>, PRL-1+) in orbital fibroblast (OF) with GO patients.<h4>Methods</h4>PD-MSCs isolated from human placenta were transfected with the PRL-1 gene using nonviral transfection method. Primary OFs were isolated from orbital adipose tissue specimens from GO patients. After maturation as adipogen","dates":{"release":"2020-01-01T00:00:00Z","publication":"2020 Nov","modification":"2025-04-22T08:42:42.579Z","creation":"2025-04-05T22:35:31.518Z"},"accession":"S-EPMC7643360","cross_references":{"pubmed":["33153489"],"doi":["10.1186/s13287-020-01982-3"]}}