Mechanosensitive miRNAs in Cartilage and Subchondral Bone Remodeling: Emerging Targets for Osteoarthritis Therapy

Evidence from laboratory and animal studies provides groundwork for understanding mechanisms and potential before human studies continue.

• Level A · Stronger Clinical Evidence
• Level B · Emerging clinical evidence with positive signals
• Level C · Early human research exploring benefits
• Level D · Scientific groundwork from lab and animal studies
• Emerging · Emerging topic under active research

Abstract (original English)

Osteoarthritis (OA) is a chronic degenerative joint disorder characterized by cartilage degradation and bone remodeling. Mechanical stimuli play fundamental roles in maintaining joint homeostasis by regulating cellular metabolism and the composition and stiffness of the extracellular matrix (ECM). Consequently, targeting mechanics-associated factors represent a promising therapeutic direction for OA. MicroRNAs (miRNAs), a class of short non-coding RNAs, negatively regulate target mRNAs at the posttranscriptional level and modulate gene expression in recipient cells without altering gene sequences. Growing interest surrounds the impact of mechanical forces on cellular responses and associated epigenetic gene expression. Therefore, investigating miRNA expression under mechanical loading conditions is crucial for elucidating the role of mechanosensitive miRNAs in articular cartilage and bone metabolism. This highlights specific miRNAs as potential therapeutic targets to disrupt the pathological feedback loops in OA. In this review, we examine the current applications of mechanosensitive miRNAs and delivery systems for OA therapy. We further analyze potential factors influencing their application. Significantly, extracellular vesicles (EVs) may facilitate the transport of mechanosensitive miRNAs across the bone-cartilage interface under mechanical stress. This mechanism provides a

Evidence level

Evidence from laboratory and animal studies provides groundwork for understanding mechanisms and potential before human studies continue.

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