Astragalus Promotes Osteogenic Differentiation of hBMSCs and Alleviates Osteoporosis by Targeting SOX11 Via miR-181d-5p.
- Author:
Yuan XIAO
1
;
Yong Li SITU
2
;
Ting Ting WANG
2
;
Shang KONG
2
;
Jiang Qi LIU
3
;
Hong NIE
2
Author Information
- Publication Type:Journal Article
- Keywords: Astragalus; MicroRNA-181d-5p; Osteogenic differentiation; Osteoporosis; SOX11
- MeSH: Osteogenesis/drug effects*; Animals; MicroRNAs/genetics*; Mesenchymal Stem Cells/drug effects*; Osteoporosis/drug therapy*; Humans; Cell Differentiation/drug effects*; Astragalus Plant/chemistry*; Rats; Rats, Sprague-Dawley; Female; SOXC Transcription Factors/genetics*; Plant Extracts/pharmacology*; Cells, Cultured; Drugs, Chinese Herbal/pharmacology*
- From: Biomedical and Environmental Sciences 2025;38(10):1287-1301
- CountryChina
- Language:English
-
Abstract:
OBJECTIVE:This study aimed to investigate the effect of Astragalus (AST) on osteoporosis (OP) and the downstream mechanisms.
METHODS:Human bone marrow-derived mesenchymal stem cells (hBMSCs) were induced to differentiate into osteogenic cells. After transfection with relevant plasmids, cell proliferation, cell cycle progression, and apoptosis were assessed. Alizarin red staining was used to detect calcium nodules in the cells, alkaline phosphatase (ALP) staining was used to detect ALP activity in the cells, and quantitative reverse transcription-polymerase chain reaction and western blotting were used to determine RUNX2 and Osterix expression levels. An OP rat model was established using ovariectomy and micro-computed tomography scanning. Hematoxylin and eosin staining and Masson's trichrome staining were used to evaluate the pathological conditions of bone tissues, while immunohistochemistry was conducted to detect RUNX2 in bone tissues.
RESULTS:AST promoted the osteogenic differentiation of BMSCs, reduced miR-181d-5p expression levels, and increased SOX11 expression levels. Restoring miR-181d-5p expression or reducing SOX11 expression levels reversed the effects of AST on the osteogenic differentiation of hBMSCs. miR-181d-5p was found to target SOX11 in hBMSCs. AST improved OP in rats, and miR-181d-5p overexpression or SOX11 inhibition reversed the therapeutic effects of AST on OP in rats.
CONCLUSION:AST promoted the osteogenic differentiation of hBMSCs and alleviated OP by targeting SOX11 via miR-181d-5p.
