期刊
MOLECULAR MEDICINE REPORTS
卷 23, 期 5, 页码 -出版社
SPANDIDOS PUBL LTD
DOI: 10.3892/mmr.2021.11989
关键词
berberine; bone marrow-derived mesenchymal stem cells; osteogenesis; adipogenesis; lipopolysaccharide
资金
- Natural Science Foundation of Shanghai [19ZR1439600]
- Natural Science Talent Cultivation Foundation of Shanghai Tenth People's Hospital [040318055]
The study showed that berberine hydrochloride (BBR) can modulate the imbalance between osteogenesis and adipogenesis mediated by Lipopolysaccharide (LPS) from oral pathogenic bacteria, potentially reversing the effects of LPS on gene expression and demonstrating the involvement of AMP-activated protein kinase.
Lipopolysaccharide (LPS) from oral pathogenic bacteria is an important factor leading to alveolar bone absorption and the implant failure. The present study aimed to evaluate the modulation of berberine hydrochloride (BBR) on the LPS-mediated osteogenesis and adipogenesis imbalance in rat bone marrow-derived mesenchymal stem cells (BMSCs). Cell viability, osteoblastic and adipogenic differentiation levels were measured using the Cell Counting Kit-8 assay, alkaline phosphatase (ALP) staining and content assay, and oil red O staining, respectively. Reverse transcription-quantitative PCR and immunoblotting were used to detect the related gene and protein expression levels. In undifferentiated cells, BBR increased the mRNA expression levels of the osteoblastic genes (Alp, RUNX family transcription factor 2, osteocalcin and secreted phosphoprotein 1) but not the adipogenic genes (fatty acid binding protein 4, Adipsin and peroxisome proliferator-activated receptor gamma). LPS-induced osteoblastic gene downregulation, adipogenic gene enhancement and NF-kappa B activation were reversed by BBR treatment. In osteoblastic differentiated cells, decreased ALP production by LPS treatment was recovered with BBR co-incubation. In adipogenic differentiated cells, LPS-mediated lipid accumulation was decreased by BBR administration. The mRNA expression levels of the pro-inflammatory factors (MCP-1, TNF-alpha, IL-6 and IL-1 beta) were increased by LPS under both adipogenic and osteoblastic conditions, which were effectively ameliorated by BBR. The actions of BBR were attenuated by compound C, suggesting that the role of BBR may be partly due to AMP-activated protein kinase activation. The results demonstrated notable pro-osteogenic and anti-adipogenic actions of BBR in a LPS-stimulated inflammatory environment. This indicated a potential role of BBR for bacterial infected-related peri-implantitis medication.
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