Zhou Shuzuo, Zhang Gang, Wang Kun, Yang Zhong, Tan Yinghui
Department of Stomatology, Second Affiliated Hospital of Army Military Medical University (Xin Qiao Hospital), Chongqing City 400038, China.
Stem Cells Int. 2023 Feb 3;2023:9094092. doi: 10.1155/2023/9094092. eCollection 2023.
PURPOSE: To explore the expression of miR-141-3p during the osteogenic differentiation of human bone marrow mesenchymal stem cells (BMSCs) and its regulatory effect. METHODS: Differentiation of BMSCs was induced by dexamethasone. The mRNA expression of miR-141-3p, ALP, RUNX2, and OCN was measured using RT-qPCR. The protein expression was detected via western blot. The target of miR-141-3p was predicted through the TargetScan website and confirmed using luciferase reporter assay. RESULTS: miR-141-3p expression declined during osteogenic differentiation. The relative ALP activities and the mRNA expression of ALP, RUNX2, and OCN were markedly reduced in the miR-141-3p mimic group while increased in the inhibitor group. Cell viability was suppressed in the miR-141-3p mimic group and promoted in the inhibitor group. SIRT1 was predicted to be a downstream gene of miR-141-3p, and this prediction was confirmed via the luciferase reporter assay. The results of the western blot assay demonstrated that SIRT1 expression was decreased in the miR-141-3p mimic group. SIRT1 reversed the inhibitory influence of miR-141-3p on the osteogenic differentiation ability of BMSCs. CONCLUSION: miR-141-3p targeted SIRT1 to inhibit osteogenic differentiation of BMSCs via the Wnt/-catenin signaling pathway.
Nan Fang Yi Ke Da Xue Xue Bao. 2018-8-30
Front Endocrinol (Lausanne). 2021
Curr Stem Cell Res Ther. 2021
Periodontol 2000. 2020-10
Aging (Albany NY). 2020-7-23