Ye S, Ju B, Wang H, Lee K-B
Department of Orthopaedic Surgery, Chonbuk National University Medical School, Research Institute of Clinical Medicine of Chonbuk National University-Biomedical Research, Institute of Chonbuk National University Hospital, Jeonju, Korea.
Chonbuk National University Medical School, Research Institute of Clinical Medicine of Chonbuk National University-Biomedical Research, Institute of Chonbuk National University Hospital, Jeonju, Korea.
Bone Joint Res. 2016 Sep;5(9):412-8. doi: 10.1302/2046-3758.59.BJR-2016-0032.R1.
Interleukin 18 (IL-18) is a regulatory cytokine that degrades the disc matrix. Bone morphogenetic protein-2 (BMP-2) stimulates synthesis of the disc extracellular matrix. However, the combined effects of BMP-2 and IL-18 on human intervertebral disc degeneration have not previously been reported. The aim of this study was to investigate the effects of the anabolic cytokine BMP-2 and the catabolic cytokine IL-18 on human nucleus pulposus (NP) and annulus fibrosus (AF) cells and, therefore, to identify potential therapeutic and clinical benefits of recombinant human (rh)BMP-2 in intervertebral disc degeneration.
Levels of IL-18 were measured in the blood of patients with intervertebral disc degenerative disease and in control patients. Human NP and AF cells were cultured in a NP cell medium and treated with IL-18 or IL-18 plus BMP-2. mRNA levels of target genes were measured by real-time polymerase chain reaction, and protein levels of aggrecan, type II collagen, SOX6, and matrix metalloproteinase 13 (MMP13) were assessed by western blot analysis.
The serum level of patients (IL-18) increased significantly with the grade of IVD degeneration. There was a dramatic alteration in IL-18 level between the advanced degeneration (Grade III to V) group and the normal group (p = 0.008) Furthermore, IL-18 induced upregulation of the catabolic regulator MMP13 and downregulation of the anabolic regulators aggrecan, type II collagen, and SOX6 at 24 hours, contributing to degradation of disc matrix enzymes. However, BMP-2 antagonised the IL-18 induced upregulation of aggrecan, type II collagen, and SOX6, resulting in reversal of IL-18 mediated disc degeneration.
BMP-2 is anti-catabolic in human NP and AF cells, and its effects are partially mediated through provocation of the catabolic effect of IL-18. These findings indicate that BMP-2 may be a unique therapeutic option for prevention and reversal of disc degeneration.Cite this article: S. Ye, B. Ju, H. Wang, K-B. Lee. Bone morphogenetic protein-2 provokes interleukin-18-induced human intervertebral disc degeneration. Bone Joint Res 2016;5:412-418. DOI: 10.1302/2046-3758.59.BJR-2016-0032.R1.
白细胞介素18(IL - 18)是一种可降解椎间盘基质的调节性细胞因子。骨形态发生蛋白2(BMP - 2)可刺激椎间盘细胞外基质的合成。然而,BMP - 2和IL - 18对人类椎间盘退变的联合作用此前尚未见报道。本研究旨在探讨合成代谢细胞因子BMP - 2和分解代谢细胞因子IL - 18对人髓核(NP)和纤维环(AF)细胞的影响,从而确定重组人(rh)BMP - 2在椎间盘退变中的潜在治疗和临床益处。
测量椎间盘退行性疾病患者和对照患者血液中的IL - 18水平。将人NP和AF细胞在NP细胞培养基中培养,并用IL - 18或IL - 18加BMP - 2处理。通过实时聚合酶链反应测量靶基因的mRNA水平,通过蛋白质印迹分析评估聚集蛋白聚糖、II型胶原蛋白、SOX6和基质金属蛋白酶13(MMP13)的蛋白质水平。
患者血清IL - 18水平随椎间盘退变程度显著升高。在晚期退变(III至V级)组和正常组之间,IL - 18水平有显著变化(p = 0.008)。此外,IL - 18在24小时时诱导分解代谢调节因子MMP13上调,合成代谢调节因子聚集蛋白聚糖、II型胶原蛋白和SOX6下调,导致椎间盘基质酶降解。然而,BMP - 2拮抗IL - 18诱导的聚集蛋白聚糖、II型胶原蛋白和SOX6上调,导致IL - 18介导的椎间盘退变逆转。
BMP - 2在人NP和AF细胞中具有抗分解代谢作用,其作用部分通过激发IL - 18的分解代谢作用介导。这些发现表明,BMP - 2可能是预防和逆转椎间盘退变的独特治疗选择。引用本文:S. Ye,B. Ju,H. Wang,K - B. Lee。骨形态发生蛋白2激发白细胞介素18诱导的人类椎间盘退变。骨关节研究2016;5:412 - 418。DOI:10.1302/2046 - 3758.59.BJR - 2016 - 0032.R1。