Reciprocal inhibition between miR-26a and NF-[kappa]B regulates obesity-related chronic inflammation in chondrocytes

• Published in: Bioscience reports 2015-06, Vol.35 (3)
• Main Authors: Xie, Qingyun, Wei, Meng, Kang, Xia, Liu, Da, Quan, Yi, Pan, Xianming, Liu, Xiling, Liao, Dongfa, Liu, Jinbiao, Zhang, Bo
• Format: Article
• Language: English
• ISSN: 0144-8463; 1573-4935
• DOI: 10.1042/BSR20150071

Obesity is causally linked to osteoarthritis (OA), with the mechanism being not fully elucidated. miRNAs (miRs) are pivotal regulators of various diseases in multiple tissues, including inflammation in the chondrocytes. In the present study, we for the first time identified the expression of miR-26a in mouse chondrocytes. Decreased level of miR-26a was correlated to increased chronic inflammation in the chondrocytes and circulation in obese mouse model. Mechanistically, we demonstrated that miR-26a attenuated saturated free fatty acid-induced activation of NF-[kappa]B (p65) and production of proinflammatory cytokines in chondrocytes. Meanwhile, NF-[kappa]B (p65) also suppressed miR-26a production by directly binding to a predicted NF-[kappa]B binding element in the promoter region of miR-26a. Finally, we observed a negative correlation between NF-[kappa]B and miR-26a in human patients with osteoarthritis. Thus, we identified a reciprocal inhibition between miR-26a and NF-[kappa]B downstream of non-esterified fatty acid (NEFA) signalling in obesity-related chondrocytes. Our findings provide a potential mechanism linking obesity to cartilage inflammation.