KDM6A promotes chondrogenic differentiation of periodontal ligament stem cells by demethylation of SOX9. (23rd November 2017)

• Record Type: Journal Article
• Authors: Wang, Pingting; Li, Yanjing; Meng, Tingting; Zhang, Junjiang; Wei, Yuanyuan; Meng, Zhaosong; Lin, Yunfeng; Liu, Dayong; Sui, Lei
• Is Part Of: Cell proliferation. Volume 51:Number 3(2018)
• Page Start: n/a
• Page End: n/a
• Publication Date: 2017-11-23
• Subjects: chondrogenesis -- KDM6A -- periodontal ligment stem cells -- SOX9; Cell proliferation -- Periodicals; 571.84
• DOI: 10.1111/cpr.12413
• Languages: English
• ISSNs: 0960-7722

Abstract

Abstract: Objectives: KDM6A has been demonstrated critical in the regulation of cell fates. However, whether KDM6A is involved in cartilage formation remains unclear. In this study, we investigated the role of KDM6A in chondrogenic differentiation of PDLSCs, as well as the underlying epigenetic mechanisms. Methods: KDM6A shRNA was transfected into PDLSCs by lentivirus. The chondrogenic differentiation potential of PDLSCs was assessed by Alcian blue staining. Immunofluorescence was performed to demonstrate H3K27me3 and H3K4me3 levels during chondrogenesis. SOX9, Col2a1, ACAN and miRNAs (miR‐29a, miR‐204, miR‐211) were detected by real‐time RT‐PCR. Western blot was performed to evaluate SOX9, H3K27me3 and H3K4me3. Results: The production of proteoglycans in PDLSCs was decreased after knockdown of KDM6A. Depletion of KDM6A inhibited the expression of SOX9, Col2a1, ACAN and resulted in increased H3K27me3 and decreased H3K4me3 levels. EZH2 inhibitor rescued the chondrogenic potential of PDLSCs after knockdown of KDM6A by regulating H3K27me3. Additionally, miR‐29a, miR‐204 and miR‐211 were also involved in the process of PDLSCs chondrogenesis. Conclusions: KDM6A is required in chondrogenic differentiation of PDLSCs by demethylation of H3K27me3, and EZH2 inhibitor could rescue chondrogenesis of PDLSCs after knockdown of KDM6A. It could be inferred that upregulation of KDM6A or application of EZH2 inhibitor might improve mesenchymal stem cell mediated cartilage regeneration in inflammatory tissue destruction such as osteoarthritis.