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2 dyn/cm 切变力上调人软骨细胞中 Kruppel 样因子 4 的表达,抑制白细胞介素-1β 激活的核因子-κB。

2 dyn/cm shear force upregulates kruppel-like factor 4 expression in human chondrocytes to inhibit the interleukin-1β-activated nuclear factor-κB.

机构信息

Department of Medical Research and Development, Chang Gung Memorial Hospital Chiayi Branch, Chiayi, Taiwan.

Department of Orthopaedics, Chang Gung Memorial Hospital Chiayi Branch, Chiayi, Taiwan.

出版信息

J Cell Physiol. 2018 Jan;234(1):958-968. doi: 10.1002/jcp.26924. Epub 2018 Aug 21.

Abstract

The shear force effect on human chondrocytes is time and magnitude dependent. Recently, kruppel-like factor (KLF) 4 has been identified as a pleiotropic protein and its activity in cells is dependent on different stimuli and/or cell types. The role of KLF4 in chondrocytes is still unclear and there has been no report determining whether shear force regulates KLF4 levels in chondrocytes. Hence, this study was carried out to investigate the role of KLF4 in human chondrocytes under shear force stimulation and the underlying mechanism. Human primary and SW1353 chondrocytes were used in this study. The shear forces at 2, 5, or 15 dyn/cm intensity were applied to both types of human chondrocytes. The specific small interfering RNAs, activators, and inhibitors were used to study the detailed mechanism of shear force. The presented results showed that 2, but not 5 and 15, dyn/cm shear force increases KLF4 expression in human primary and SW1353 chondrocytes. Extracellular signal-regulated kinase 5 induced peroxisome proliferator-activated receptor γ transcription activity to increase KLF4 transcription. Moreover, the KLF4 induction in human chondrocytes in response to 2 dyn/cm shear force could attenuate interleukin (IL)-1β-stimulated nuclear factor-κB activation. These results elucidate the role of KLF4 in antagonizing the effect of IL-1β in human chondrocytes under 2 dyn/cm shear force stimulation and provide a possible mechanism to demonstrate the protection of moderate forces or exercises in cartilage.

摘要

切应力对人软骨细胞的作用具有时间和幅度依赖性。最近,Krüppel 样因子(KLF)4 已被确定为一种多功能蛋白,其在细胞中的活性取决于不同的刺激和/或细胞类型。KLF4 在软骨细胞中的作用尚不清楚,也没有报道确定切应力是否调节软骨细胞中的 KLF4 水平。因此,本研究旨在探讨 KLF4 在切应力刺激下人软骨细胞中的作用及其潜在机制。本研究使用了人原代和 SW1353 软骨细胞。将 2、5 或 15 dyn/cm 强度的切应力应用于两种类型的人软骨细胞。使用特定的小干扰 RNA、激活剂和抑制剂来研究切应力的详细机制。结果表明,2 dyn/cm 切应力而非 5 和 15 dyn/cm 切应力增加了人原代和 SW1353 软骨细胞中的 KLF4 表达。细胞外信号调节激酶 5 诱导过氧化物酶体增殖物激活受体 γ 转录活性以增加 KLF4 转录。此外,2 dyn/cm 切应力作用下人软骨细胞中 KLF4 的诱导可减弱白细胞介素(IL)-1β刺激的核因子-κB 激活。这些结果阐明了 KLF4 在拮抗 2 dyn/cm 切应力刺激下人软骨细胞中 IL-1β作用的作用,并提供了一种可能的机制来证明中等强度的力或运动对软骨的保护作用。

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