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循环机械应力通过基质金属蛋白酶和白细胞介素-1的基因表达诱导培养的软骨细胞中细胞外基质降解。

Cyclic mechanical stress induces extracellular matrix degradation in cultured chondrocytes via gene expression of matrix metalloproteinases and interleukin-1.

作者信息

Fujisawa T, Hattori T, Takahashi K, Kuboki T, Yamashita A, Takigawa M

机构信息

Department of Biochemistry and Molecular Dentistry, Okayama University Dental School, Okayama, 700-8525, Japan.

出版信息

J Biochem. 1999 May;125(5):966-75. doi: 10.1093/oxfordjournals.jbchem.a022376.

DOI:10.1093/oxfordjournals.jbchem.a022376
PMID:10220591
Abstract

To clarify the mechanism of cartilage degradation induced by mechanical stress, we investigated the influence of cyclic tension force (CTF) on the metabolism of cultured chondrocytes. The chondrocytes were exposed to CTF using a Flexercell strain unit. Five or 15 kPa of high frequency CTF significantly inhibited the syntheses of DNA, proteoglycan, collagen, and protein. Fifteen kPa of high frequency CTF induced the expression of interleukin-1 (IL-1), matrix metalloproteinase (MMP)-2 and -9 mRNA, and increased the production of pro- and active-MMP-9. The degradation of proteoglycan was inhibited by and MMP inhibitor, indicating that MMPs are involved in the degradation of proteoglycans induced by high frequency CTF. Moreover, reducing the frequency of CTF from high to low decreased the inhibition of proteoglycan synthesis. These findings suggest that the CTF frequency is one of the key determinants of chondrocyte metabolism. Low magnitude CTF, whether high or low frequency, did not cause the gene expression of cartilage degradation factors, suggesting that this CTF magnitude causes only minor changes in the cartilage matrix. High magnitude and frequency CTF caused the gene expression of IL-1 and MMP-9, followed by increases in the production of MMP-2 and -9 proteins, suggesting that excessive and continuous cyclic mechanical stress induces the production of IL-1 and MMP-9, resulting in cartilage degradation.

摘要

为阐明机械应力诱导软骨降解的机制,我们研究了周期性张力(CTF)对培养软骨细胞代谢的影响。使用Flexercell应变装置使软骨细胞暴露于CTF。5kPa或15kPa的高频CTF显著抑制DNA、蛋白聚糖、胶原蛋白和蛋白质的合成。15kPa的高频CTF诱导白细胞介素-1(IL-1)、基质金属蛋白酶(MMP)-2和-9mRNA的表达,并增加前MMP-9和活性MMP-9的产生。蛋白聚糖的降解被MMP抑制剂抑制,表明MMP参与高频CTF诱导的蛋白聚糖降解。此外,将CTF频率从高降低到低可减少对蛋白聚糖合成的抑制。这些发现表明CTF频率是软骨细胞代谢的关键决定因素之一。低强度CTF,无论高频还是低频,均未引起软骨降解因子的基因表达,表明这种CTF强度仅导致软骨基质的微小变化。高强度和高频CTF导致IL-1和MMP-9的基因表达,随后MMP-2和-9蛋白的产生增加,表明过度和持续的周期性机械应力诱导IL-1和MMP-9的产生,导致软骨降解。

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