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首页> 外文期刊>Arthritis research & therapy. >The involvement of interleukin-1 and interleukin-4 in the response of human annulus fibrosus cells to cyclic tensile strain: an altered mechanotransduction pathway with degeneration.
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The involvement of interleukin-1 and interleukin-4 in the response of human annulus fibrosus cells to cyclic tensile strain: an altered mechanotransduction pathway with degeneration.

机译:白细胞介素1和白细胞介素4参与人类纤维环细胞对循环拉伸应变的响应:变性的改变的机械转导途径。

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INTRODUCTION: Recent evidence suggests that intervertebral disc (IVD) cells derived from degenerative tissue are unable to respond to physiologically relevant mechanical stimuli in the 'normal' anabolic manner, but instead respond by increasing matrix catabolism. Understanding the nature of the biological processes which allow disc cells to sense and respond to mechanical stimuli (a process termed 'mechanotransduction') is important to ascertain whether these signalling pathways differ with disease. The aim here was to investigate the involvement of interleukin (IL)-1 and IL-4 in the response of annulus fibrosus (AF) cells derived from nondegenerative and degenerative tissue to cyclic tensile strain to determine whether cytokine involvement differed with IVD degeneration. METHODS: AF cells were isolated from nondegenerative and degenerative human IVDs, expanded in monolayers and cyclically strained in the presence or absence of the cytokine inhibitors IL-1 receptor antagonist (IL-1Ra) or IL-4 receptor antibody (IL-4RAb) with 10% strain at 1.0 Hz for 20 minutes using a Flexcell strain device. Total RNA was extracted from the cells at time points of baseline control and 1 or 24 hours poststimulation. Quantitative real-time polymerase chain reaction was used to analyse the gene expression of matrix proteins (aggrecan and type I collagen) and enzymes (matrix metalloproteinase 3 (MMP3) and a disintegrin and metalloproteinase with a thrombospondin type 1 motif 4 (ADAMTS4)). RESULTS: Expression of catabolic genes (MMP3 and ADAMTS4) decreased in AF cells derived from nondegenerative tissue in response to 1.0-Hz stimulation, and this decrease in gene expression was inhibited or increased following pretreatment of cells with IL-1Ra or IL-4RAb respectively. Treatment of AF cells derived from degenerative tissue with an identical stimulus (1.0-Hz) resulted in reduced anabolic gene expression (aggrecan and type I collagen), with IL-1Ra or IL-4RAb pretreatment having no effect. CONCLUSIONS: Both IL-1 and IL-4 are involved in the response of AF cells derived from nondegenerative tissue to 1.0-Hz cyclic tensile strain. Interestingly, the altered response observed at 1.0-Hz in AF cells from degenerative tissue appears to be independent of either cytokine, suggesting an alternative mechanotransduction pathway in operation.
机译:引言:最近的证据表明,源自变性组织的椎间盘(IVD)细胞无法以“正常”合成代谢方式对生理相关的机械刺激做出反应,而是通过增加基质分解代谢来做出反应。理解允许椎间盘细胞感知并响应机械刺激的生物学过程的本质(一种称为“机械转导”的过程)对于确定这些信号通路是否随疾病而异很重要。此处的目的是研究白介素(IL)-1和IL-4在源自非变性和变性组织的纤维环(AF)细胞对循环拉伸应变的反应中的参与,以确定细胞因子的参与是否与IVD变性有所不同。方法:从非变性和变性人类IVDs中分离AF细胞,在存在或不存在细胞因子抑制剂IL-1受体拮抗剂(IL-1Ra)或IL-4受体抗体(IL-4RAb)的情况下,单层扩增并循环应变。使用Flexcell应变装置在1.0 Hz下10%应变20分钟。在基线对照和刺激后1或24小时的时间点从细胞中提取总RNA。实时定量聚合酶链反应用于分析基质蛋白(聚集蛋白聚糖和I型胶原蛋白)和酶(基质金属蛋白酶3(MMP3)和具有1型血小板反应蛋白基序4(ADAMTS4)的双整合蛋白和金属蛋白酶)的基因表达。结果:在1.0 Hz刺激下,来自非变性组织的AF细胞中分解代谢基因(MMP3和ADAMTS4)的表达降低,并且在分别用IL-1Ra或IL-4RAb预处理细胞后,该基因表达的降低被抑制或增加。 。用相同的刺激(1.0-Hz)处理源自变性组织的AF细胞会导致合成代谢基因表达降低(聚集蛋白聚糖和I型胶原蛋白),而IL-1Ra或IL-4RAb预处理无效。结论:IL-1和IL-4均参与了非变性组织对1.0Hz循环拉伸应变的AF细胞的应答。有趣的是,在变性细胞的AF细胞中以1.0 Hz观察到的响应改变似乎独立于任何一种细胞因子,提示在操作中存在另一种机械转导途径。

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