| Literature DB >> 34822133 |
Changwei Yang1,2, Xuehong Xu1, Pingting Lin1, Bizhu Luo1, Shufang Luo1, Honglan Huang1, Jianyu Zhu1, Meie Huang1, Shuhai Peng3, Qianju Wu1, Lu Yin4,5.
Abstract
MCM3AP-AS1 regulates the cartilage repair in osteoarthritis, but how it regulates osteogenic differentiation of dental pulp stem cells (DPSCs) remains to be determined. DPSCs were isolated and induced for osteogenic differentiation. MCM3AP-AS1 expression was increased along with the osteogenic differentiation of DPSCs, whose expression was positive correlated with those of OCN, alkaline phosphatase (ALP) and RUNX2. On contrary, miR-143-3p expression was decreased along with the osteogenic differentiation and was negatively correlated with those of OCN, ALP and RUNX2. Dual-luciferase reporter gene assay showed that miR-143-3p can be negatively regulated by MCM3AP-AS1 and can regulate IGFBP5. MCM3AP-AS1 overexpression increased the expression levels of osteogenesis-specific genes, ALP activity and mineralized nodules during DPSC osteogenic differentiation, while IGFBP5 knockdown or miR-143-3p overexpression counteracted the effect of MCM3AP-AS1 overexpression in DPSCs. Therefore, this study demonstrated the role of MCM3AP-AS1/miR-143-3p/IGFBP5 axis in regulating DPSC osteogenic differentiation.Entities:
Keywords: Dental pulp stem cell; IGFBP5; MCM3AP-AS1; Osteogenic differentiation; miR-143-3p
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Year: 2021 PMID: 34822133 DOI: 10.1007/s13577-021-00648-3
Source DB: PubMed Journal: Hum Cell ISSN: 0914-7470 Impact factor: 4.174