Ozawa Masatsugu, Nishida Keiichiro, Yoshida Aki, Saito Taichi, Harada Ryozo, Machida Takahiro, Ozaki Toshifumi
Department of Orthopaedic Surgery, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, 2-5-1 Shikata-cho, Okayama City, Okayama, 700-8558, Japan.
Inflamm Res. 2015 Apr;64(3-4):243-52. doi: 10.1007/s00011-015-0804-2. Epub 2015 Feb 19.
To investigate the inhibitory effect of hyaluronan (HA) on mechanical stress- induced expression of a disintegrin and metalloproteinase with thrombospondin type 1 motifs (ADAMTS)-4, -5 and matrix metalloproteinase (MMP)-13 by human chondrocytes.
Normal human articular chondrocytes were pre-incubated with or without 1.0 mg/mL HA (2700 kDa) for 12 h at 37 °C in stretch chambers, then they were exposed to uni-axial cyclic tensile strain (CTS, 0.5 Hz, 10% elongation). The expression of ADAMTS-4, -5, and MMP-13 were analyzed by real-time polymerase chain reaction and Immunocytochemistry. The concentration of IL-1β in the supernatant was measured using enzyme-linked immunosorbent assay (ELISA). The nuclear translocation of runt-related transcription factor 2 (RUNX-2) and nuclear factor-κB (NF-κB) was examined by ELISA and immunocytochemistry, and phosphorylation of NF-κB was examined by western blotting.
HA inhibited mRNA expression of ADAMTS-4, -5, and MMP13 after 24 h CTS via inhibition of IL-1β secretion and NF-κB activation. However, HA failed to inhibit CTS-induced RUNX-2 expression and subsequent expression of ADAMTS-5 and MMP-13 1 h after CTS.
Our results demonstrated that HA significantly suppressed mechanical stress-induced expression of catabolic proteases by inhibition of the NF-κB-IL-1β pathway, but did not suppress mechanical stress-induced RUNX-2 signaling.
研究透明质酸(HA)对人软骨细胞机械应力诱导的含血小板反应蛋白基序的解聚素和金属蛋白酶(ADAMTS)-4、-5以及基质金属蛋白酶(MMP)-13表达的抑制作用。
将正常人关节软骨细胞在拉伸培养箱中于37℃预孵育12小时,分别添加或不添加1.0mg/mL HA(2700kDa),然后使其暴露于单轴循环拉伸应变(CTS,0.5Hz,10%伸长率)。通过实时聚合酶链反应和免疫细胞化学分析ADAMTS-4、-5和MMP-13的表达。使用酶联免疫吸附测定(ELISA)测量上清液中白细胞介素-1β(IL-1β)的浓度。通过ELISA和免疫细胞化学检测 runt相关转录因子2(RUNX-2)和核因子-κB(NF-κB)的核转位,并通过蛋白质印迹法检测NF-κB的磷酸化。
HA通过抑制IL-1β分泌和NF-κB激活,在CTS处理24小时后抑制了ADAMTS-4、-5和MMP13的mRNA表达。然而,HA未能抑制CTS诱导的RUNX-2表达以及CTS处理1小时后ADAMTS-5和MMP-13的后续表达。
我们的结果表明,HA通过抑制NF-κB-IL-1β途径显著抑制了机械应力诱导的分解代谢蛋白酶的表达,但未抑制机械应力诱导的RUNX-2信号传导。