circ_0003204 regulates the osteogenic differentiation of human adipose-derived stem cells via miR-370-3p/HDAC4 axis

Bibliographic Details
Title: circ_0003204 regulates the osteogenic differentiation of human adipose-derived stem cells via miR-370-3p/HDAC4 axis
Authors: Liyuan Yu, Kai Xia, Jing Zhou, Zhiai Hu, Xing Yin, Chenchen Zhou, Shujuan Zou, Jun Liu
Source: International Journal of Oral Science, Vol 14, Iss 1, Pp 1-11 (2022)
Publisher Information: Nature Publishing Group, 2022.
Publication Year: 2022
Collection: LCC:Dentistry
Subject Terms: Dentistry, RK1-715
More Details: Abstract Human adipose-derived stem cells (hASCs) are a promising cell type for bone tissue regeneration. Circular RNAs (circRNAs) have been shown to play a critical role in regulating various cell differentiation and involve in mesenchymal stem cell osteogenesis. However, how circRNAs regulate hASCs in osteogenesis is still unclear. Herein, we found circ_0003204 was significantly downregulated during osteogenic differentiation of hASCs. Knockdown of circ_0003204 by siRNA or overexpression by lentivirus confirmed circ_0003204 could negatively regulate the osteogenic differentiation of hASCs. We performed dual-luciferase reporting assay and rescue experiments to verify circ_0003204 regulated osteogenic differentiation via sponging miR-370-3p. We predicted and confirmed that miR-370-3p had targets in the 3′-UTR of HDAC4 mRNA. The following rescue experiments indicated that circ_0003204 regulated the osteogenic differentiation of hASCs via miR-370-3p/HDAC4 axis. Subsequent in vivo experiments showed the silencing of circ_0003204 increased the bone formation and promoted the expression of osteogenic-related proteins in a mouse bone defect model, while overexpression of circ_0003204 inhibited bone defect repair. Our findings indicated that circ_0003204 might be a promising target to promote the efficacy of hASCs in repairing bone defects.
Document Type: article
File Description: electronic resource
Language: English
ISSN: 1674-2818
2049-3169
Relation: https://doaj.org/toc/1674-2818; https://doaj.org/toc/2049-3169
DOI: 10.1038/s41368-022-00184-2
Access URL: https://doaj.org/article/6cb36dd79852450b9b732e0cf869172d
Accession Number: edsdoj.6cb36dd79852450b9b732e0cf869172d
Database: Directory of Open Access Journals
More Details
ISSN:16742818
20493169
DOI:10.1038/s41368-022-00184-2
Published in:International Journal of Oral Science
Language:English