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成纤维细胞生长因子2抑制人关节软骨中聚集蛋白聚糖酶活性的诱导。

Fibroblast growth factor 2 inhibits induction of aggrecanase activity in human articular cartilage.

作者信息

Sawaji Yasunobu, Hynes Judith, Vincent Tonia, Saklatvala Jeremy

机构信息

Imperial College London, London, UK.

出版信息

Arthritis Rheum. 2008 Nov;58(11):3498-509. doi: 10.1002/art.24025.

Abstract

OBJECTIVE

Articular chondrocytes are surrounded by an extracellular pool of fibroblast growth factor 2 (FGF-2). We undertook this study to investigate the possible role of FGF-2 in aggrecan catabolism by aggrecanase in human articular cartilage.

METHODS

Aggrecan catabolism was induced by interleukin-1alpha (IL-1alpha) in normal human articular cartilage and assessed by measuring the release of glycosaminoglycan (GAG) and aggrecanase-dependent fragments by Western blotting with antibodies against neoepitopes. ADAMTS-4 and ADAMTS-5 messenger RNA (mRNA) expression was measured by quantitative real-time reverse transcriptase-polymerase chain reaction. Production of matrix metalloproteinases (MMPs) 1, 3, and 13 and tissue inhibitors of metalloproteinases (TIMPs) 1 and 3 was measured by Western blotting. IL-6 and IL-8 were measured by enzyme-linked immunosorbent assay. Proteoglycan synthesis was monitored by 35S-sulfate incorporation.

RESULTS

IL-1alpha caused cleavage of aggrecan in cultured human articular cartilage explants, with release of GAG and aggrecan fragments containing ARGS and AGEG neoepitopes. This was inhibited by FGF-2 (1-100 ng/ml). Tumor necrosis factor alpha and retinoic acid also stimulated release of neoepitope, and this was also suppressed by FGF-2. IL-1alpha induced ADAMTS-4 and ADAMTS-5 mRNA in primary human chondrocytes, and this was inhibited by FGF-2. IL-1alpha-induced aggrecan breakdown was inhibited by TIMP-1 or by the N-terminal portion of TIMP-3, although FGF-2 did not affect production of the inhibitors TIMP-1 and TIMP-3 when IL-1alpha was present. FGF-2 did not prevent IL-1alpha suppression of proteoglycan synthesis and did not negate its ability to stimulate the production of IL-6, IL-8, and MMPs 1, 3, and 13.

CONCLUSION

Our findings suggest that FGF-2 may play a chondroprotective role in human articular cartilage by controlling the expression and activity of the aggrecanases ADAMTS-4 and ADAMTS-5.

摘要

目的

关节软骨细胞被成纤维细胞生长因子2(FGF-2)的细胞外池所包围。我们进行这项研究以调查FGF-2在人关节软骨中由聚集蛋白聚糖酶介导的聚集蛋白聚糖分解代谢中可能发挥的作用。

方法

用白细胞介素-1α(IL-1α)诱导正常人关节软骨中的聚集蛋白聚糖分解代谢,并通过用针对新表位的抗体进行蛋白质印迹法测量糖胺聚糖(GAG)和聚集蛋白聚糖酶依赖性片段的释放来评估。通过定量实时逆转录聚合酶链反应测量ADAMTS-4和ADAMTS-5信使核糖核酸(mRNA)的表达。通过蛋白质印迹法测量基质金属蛋白酶(MMP)1、3和13以及金属蛋白酶组织抑制剂(TIMP)1和3的产生。通过酶联免疫吸附测定法测量IL-6和IL-8。通过35S-硫酸盐掺入监测蛋白聚糖的合成。

结果

IL-1α导致培养的人关节软骨外植体中聚集蛋白聚糖的裂解,伴有GAG和含有ARGS和AGEG新表位的聚集蛋白聚糖片段的释放。这被FGF-2(1 - 100 ng/ml)抑制。肿瘤坏死因子α和视黄酸也刺激新表位的释放,并且这也被FGF-2抑制。IL-1α在原代人软骨细胞中诱导ADAMTS-4和ADAMTS-5 mRNA,并且这被FGF-2抑制。TIMP-1或TIMP-3的N端部分抑制IL-1α诱导的聚集蛋白聚糖分解,尽管当存在IL-1α时FGF-2不影响抑制剂TIMP-1和TIMP-3的产生。FGF-2不能阻止IL-1α对蛋白聚糖合成的抑制,也不能消除其刺激IL-6、IL-8以及MMP 1、3和13产生的能力。

结论

我们的研究结果表明,FGF-2可能通过控制聚集蛋白聚糖酶ADAMTS-4和ADAMTS-5的表达和活性在人关节软骨中发挥软骨保护作用。

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