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Oleanolic acid mitigates interleukin-1β-induced chondrocyte dysfunction by regulating miR-148-3p-modulated FGF2
Yuanli Li1, Junlan Nie1, Ping Jiang1
1Department of Orthopedics, Affiliated Hospital of North Sichuang Medical College, Nanchong, Sichuan Province, China.
The Journal of Gene Medicine
|February 7, 2020
Summary
Oleanolic acid (OLA) protects chondrocytes from interleukin-1β-induced dysfunction by regulating the miR-148-3p/FGF2 pathway. This pathway is a potential therapeutic target for osteoarthritis treatment.
Area of Science:
- Cell Biology
- Molecular Biology
- Biochemistry
Background:
- MicroRNA (miR)-mediated post-transcriptional repression contributes to chondrocyte dysfunction.
- Interleukin-1β (IL-1β) is implicated in chondrocyte dysfunction.
- Oleanolic acid (OLA) demonstrates protective effects against inflammatory stimuli in chondrocytes.
Purpose of the Study:
- To investigate the molecular mechanisms of OLA in preventing IL-1β-induced chondrocyte dysfunction.
- To elucidate the role of the miR-148-3p/fibroblast growth factor-2 (FGF-2) signaling pathway in this process.
Main Methods:
- miR microarray assays to identify candidate miRs.
- Quantitative reverse transcriptase-polymerase chain reaction (RT-qPCR) and western blotting to analyze gene and protein expression.
- Cell counting kit-8 (CCK-8) assays for cell growth and Annexin V staining for apoptosis.
Main Results:
- OLA counteracted IL-1β-induced chondrocyte growth inhibition, apoptosis, and oxidative stress markers.
- OLA and miR-148-3p mimics down-regulated IL-1β-elevated FGF2 protein expression.
- FGF2 was identified as a direct target of miR-148-3p, and miR-148-3p mimics replicated OLA's protective effects.
Conclusions:
- OLA exerts a protective effect against IL-1β-induced chondrocyte dysfunction.
- The miR-148-3p/FGF2 signaling pathway is a novel mechanism underlying OLA's action.
- This pathway represents a potential therapeutic target for osteoarthritis prevention and treatment.
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