Overexpression of miR-140-5p inhibits lipopolysaccharide-induced human intervertebral disc inflammation and degeneration by downregulating toll-like receptor 4

被引:43
|
作者
Zhang, Qiang [1 ]
Weng, Yiping [1 ]
Jiang, Yuqing [1 ]
Zhao, Shujie [1 ]
Zhou, Dong [1 ]
Xu, Nanwei [1 ]
机构
[1] Nanjing Med Univ, Dept Orthopaed, Affiliated Changzhou Peoples Hosp 2, 29 Xinglongxiang St, Changzhou 213000, Jiangsu, Peoples R China
关键词
intervertebral disc degeneration; inflammation; LPS; TLR4; miR-140-5p; ECM; MOLECULAR-MECHANISMS; TNF-ALPHA; KAPPA-B; EXPRESSION; PATHWAY; MATRIX; CELLS; PLATE; LPS; INTERLEUKIN-1;
D O I
10.3892/or.2018.6488
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Toll-like receptor 4 (TLR4) families are receptors for ligands that initiate extracellular or intracellular signaling, such as lipopolysaccharides (LPS). It has been reported that TLR4 activation resulted in the upregulation of a coordinated set of proinflammatory mediators and inhibition of matrix expression in the intervertebral disc (IVD). miR-140-5p (miR-140) is reported to participate in cellular anti-inflammatory processes and target TLR4. In the present study, we investigated the relationship between TLR4 and miR-140 in IVD degeneration. The expression of TLR4, interleukin (IL)-6, IL-I, L-1 and tumor necrosis factor (TNF)- was higher, in high-grade IVD degeneration tissues than in low-grade tissues. In contrast, the expression of miR-140, aggrecan and collagen type II was lower in high-grade IVD degeneration tissues than in low-grade IVD degeneration tissues. LPS stimulation resulted in significant increases in TLR4 expression and decreases in miR-140 expression in nucleus pulposus (NP) cells and TLR4 was identified as a target of miR-140 by dual-luciferase reporter assay. The overexpression of miR-140 inhibited the upregulation of the expression of TLR4, TNF-, IL-1 and IL-6 inflammation cytokines, and the activation of NF-B and reversed the downregulation of the expression of aggrecan and collagen type II induced by LPS stimulation. In conclusion, the present study may lead to a greater understanding of IVD degeneration and provide new insights into the treatment of this disease.
引用
收藏
页码:793 / 802
页数:10
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