Affiliation:
1. Liaoning Provincial Key Laboratory of Oral Disease, School and Hospital of Stomatology China Medical University Shenyang China
2. Department of Oral Medicine The Second Affiliated Hospital of Zhejiang University School of Medicine Hangzhou China
Abstract
AbstractAimThis study aimed to investigate the upstream regulators and specific mechanisms of metastasis‐associated lung adenocarcinoma transcript 1 (MALAT1) in the odontoblastic differentiation of human dental pulp stem cells (hDPSCs).MethodologyHuman dental pulp stem cells were isolated and cultured, followed by conducting loss‐ or gain‐of‐function experiments on ATF4 and loss experiments on MALAT1 to elucidate their respective biological functions in odontoblastic differentiation. Chromatin immunoprecipitation assays and RNA immunoprecipitation were performed to uncover the interaction between ATF4‐MALAT1 and MALAT1‐JMJD3, respectively. The odontoblastic differentiation was estimated by the mRNA and protein of DSPP and DMP1, as well as alkaline phosphatase staining.ResultsExpression of MALAT1 was upregulated in the hDPSCs cultured in an odontoblastic medium, and MALAT1 downregulation suppressed the odontoblastic differentiation of the hDPSCs. Subsequent experiments confirmed that ATF4 promoted odontoblastic differentiation and induced MALAT1 expression by binding to the MALAT1 promoter region. Further experiments revealed that nuclear MALAT1 interacted with JMJD3. MALAT1 knockdown decreased the JMJD3 protein level and demethylase activity, and it enhanced H3K27me3 occupancy of the promoter region of DSPP and DMP1, resulting in the inhibition of DSPP and DMP1 transcription. Importantly, JMJD3 overexpression significantly attenuated the inhibition of odontoblastic differentiation induced by MALAT1 knockdown.ConclusionsATF4‐regulated MALAT1 plays a positive regulatory role in odontoblastic differentiation of hDPSCs through JMJD3‐mediated H3K27me3 modifications of the DSPP and DMP1 promoters.
Funder
National Natural Science Foundation of China