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Effects of Chronic Mild Stress on the Development of Atherosclerosis and Expression of Toll-Like Receptor 4 Signaling Pathway in Adolescent Apolipoprotein E Knockout Mice

机译:慢性轻度应激对青春期载脂蛋白E基因敲除小鼠动脉粥样硬化发展和Toll样受体4信号通路表达的影响

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摘要

Here, we investigated the effect of chronic mild stress (CMS) on the development of atherosclerosis as well as the expression of Toll-like receptors (TLRs) signaling pathway in adolescent apolipoprotein E knockout (apoE-/-) mice. Mice were subjected to daily CMS for 0, 4, and 12 weeks, respectively. To identify the expression of Toll-like receptor 4 signaling pathway in adolescent apolipoprotein E knockout mice subjected to CMS, we compared gene expression in aortas of stressed and unstressed mice using TLRs signaling pathway real-time PCR microarrays consisting of 87 genes. We found that atherosclerosis lesions both in aortic tress and sinuses of CMS mice were significantly increased linearly in response to duration of CMS exposure. Among 87 genes analyzed, 15 genes were upregulated in stressed mice, especially TLR4, myeloid differentiation factor 88 (MyD88), and IL-1β, and 28 genes were downregulated compared with nonstressed mice. CMS mice demonstrated markedly increased aortic atherosclerosis that were associated with significant increases in levels of expression of TLR4, MyD88, nuclear factor κB (NF-κB), MCP-1, IL-1β, TNF-α, and sICAM-1. Taken together, our results suggest an important role for TLR4 signaling pathway in atherosclerosis in a CMS mouse model.
机译:在这里,我们调查了慢性轻度应激(CMS)对动脉粥样硬化的发展以及青春期载脂蛋白E基因敲除(apoE-/-)小鼠Toll样受体(TLRs)信号通路表达的影响。每天分别对小鼠进行0、4和12周的CMS。为了确定在接受CMS的青春期载脂蛋白E基因敲除小鼠中Toll样受体4信号通路的表达,我们使用TLRs信号通路实时PCR微阵列(由87个基因组成)比较了应激和非应激小鼠主动脉中的基因表达。我们发现,在CMS小鼠的主动脉发束和鼻窦中,动脉粥样硬化病变均随CMS暴露持续时间线性增加。在分析的87个基因中,有15个基因在应激小鼠中被上调,尤其是TLR4,髓样分化因子88(MyD88)和IL-1β,与非应激小鼠相比,有28个基因被下调。 CMS小鼠表现出主动脉粥样硬化明显增加,这与TLR4,MyD88,核因子κB(NF-κB),MCP-1,IL-1β,TNF-α和sICAM-1的表达水平显着增加有关。两者合计,我们的结果表明CMS小鼠模型中TLR4信号通路在动脉粥样硬化中具有重要作用。

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