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肥胖患者骨关节炎软骨中的软骨细胞显示出脂联素受体表达改变以及对脂联素的反应。

Chondrocytes from osteoarthritic cartilage of obese patients show altered adiponectin receptors expression and response to adiponectin.

作者信息

Harasymowicz Natalia Sara, Azfer Asim, Burnett Richard, Simpson Hamish, Salter Donald M

机构信息

Department of Orthopaedics and Trauma, The University of Edinburgh, Edinburgh, UK.

Bone Research Group, Center for Genomics and Experimental Medicine, The University of Edinburgh, Edinburgh, UK.

出版信息

J Orthop Res. 2021 Nov;39(11):2333-2339. doi: 10.1002/jor.24993. Epub 2021 Feb 1.

Abstract

Obesity and osteoarthritis (OA) are well-known comorbidities and their precise molecular interactions are still unidentified. Adiponectin, a major adipokine, known to have an anti-inflammatory effect in atherosclerosis or Type 2 Diabetes Mellitus (T2DM), has also been postulated to be pro-inflammatory in OA. This dual role of adiponectin is still not explained. The precise mechanism by which adiponectin affects cartilage and chondrocytes remains to be elucidated. In the present observational study chondrocytes from 30 patients with OA (18 females and 12 males) undergoing total knee replacement (TKR) were isolated. Expression of adiponectin receptors 1 and 2 (ADIPOR1 and ADIPOR2) was examined both at gene and protein levels in chondrocytes. The difference in adiponectin receptor expression between lean and obese patients with OA and the role of adiponectin in regulating pro-inflammatory genes (MCP-1, IL-6, and VCAM-1, MMP-1, MMP-2, and TIMP-1) has been investigated. We found that ADIPOR1 represented the most abundant adiponectin receptor in primary OA chondrocytes. ADIPOR1 and ADIPOR2 genes and ADIPOR1 protein were differently expressed in OA chondrocytes obtained from obese compared with lean patients with OA. Adiponectin induced gene expression of MCP-1, IL-6, and MMP-1 in all OA patients' chondrocytes. In contrast, VCAM-1 and MMP-2 were differently regulated by adiponectin depending on the patient's body mass index. This study suggests that adiponectin and ADIPOR1 may have important roles in the pathogenesis of cartilage degeneration in OA of obese subjects.

摘要

肥胖与骨关节炎(OA)是众所周知的共病,但其确切的分子相互作用仍不明晰。脂联素作为一种主要的脂肪因子,已知在动脉粥样硬化或2型糖尿病(T2DM)中具有抗炎作用,但也被推测在OA中具有促炎作用。脂联素的这种双重作用仍未得到解释。脂联素影响软骨和软骨细胞的确切机制仍有待阐明。在本观察性研究中,从30例行全膝关节置换术(TKR)的OA患者(18名女性和12名男性)中分离出软骨细胞。在软骨细胞中从基因和蛋白质水平检测脂联素受体1和2(ADIPOR1和ADIPOR2)的表达。研究了肥胖与非肥胖OA患者之间脂联素受体表达的差异以及脂联素在调节促炎基因(MCP-1、IL-6、VCAM-1、MMP-1、MMP-2和TIMP-1)中的作用。我们发现ADIPOR1是原发性OA软骨细胞中最丰富的脂联素受体。与非肥胖OA患者相比,肥胖OA患者的软骨细胞中ADIPOR1和ADIPOR2基因以及ADIPOR1蛋白的表达存在差异。脂联素可诱导所有OA患者软骨细胞中MCP-1、IL-6和MMP-1的基因表达。相比之下,脂联素对VCAM-1和MMP-2的调节因患者体重指数而异。本研究表明,脂联素和ADIPOR1可能在肥胖受试者OA软骨退变的发病机制中起重要作用。

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