| Literature DB >> 33453444 |
Yuanwu Cao1, Chang Jiang1, Xinyuan Wang1, Hao Wang1, Zuoqin Yan1, Hengfeng Yuan2.
Abstract
The adverse effects of glucocorticoids (GCs) on bone marrow stromal stem cells (BMSCs) play an important role in steroid-induced osteonecrosis of the femoral head (ONFH). Our previous miRNA microarray analysis indicated that microRNA-224-5p (miR-224-5p) could be a potential regulator; however, the underlying mechanism remains unclear. In the present study, we demonstrated that miR-224-5p was upregulated in GC-treated BMSCs, and functional experiments revealed that miR-224-5p could suppress osteogenic but promote adipogenic differentiation of BMSCs. Smad4 was identified as a direct target gene of miR-224-5p, and the Smad4-Taz axis was confirmed as the regulatory pathway for adipo-osteogenic differentiation of BMSCs. Our in vivo experiments further confirmed that the miR-224-5p antagomir could alleviate the inhibitory effects of GCs and facilitate bone formation in steroid-induced ONFH models. Therefore, these findings provide insight into the function of miR-224-5p as a reciprocal regulator of the adipo-osteogenic differentiation of BMSCs, and it could serve as a novel therapeutic target for steroid-induced ONFH.Entities:
Keywords: Adipogenesis; BMSCs; Osteogenesis; Osteonecrosis; microRNA-224
Mesh:
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Year: 2021 PMID: 33453444 DOI: 10.1016/j.bone.2021.115844
Source DB: PubMed Journal: Bone ISSN: 1873-2763 Impact factor: 4.398