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首页> 外文期刊>Transplantation Proceedings >The role of CD14 and Toll-like receptor 4 of Kupffer cells in hepatic ischemia-reperfusion injury in rats
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The role of CD14 and Toll-like receptor 4 of Kupffer cells in hepatic ischemia-reperfusion injury in rats

机译:库普弗细胞CD14和Toll样受体4在大鼠肝缺血再灌注损伤中的作用

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Objective: The objective of this study was to study the role of CD14 and Toll-like receptor 4 (TLR4) in Kupffer cells (KCs) on ischemia reperfusion injury (IRI) in rat liver grafts. Methods: Isolated KCs were obtained from control, IRI, and IRI plus anti-CD14 antibody groups. We measured messenger RNA (mRNA) and protein expression of the lipopolysaccharide receptor CD14 and TLR4, nuclear factor kappa B (NF-κβ) activity, and TNF-α levels. Results: mRNA and protein expressions of CD14 and TLR4 were significantly higher in the IRI than in the control group, as were protein expressions of CD14 and TLR4 by flow cytometry and by Western blots. NF-κβ activity and tumor necrosis factor-α level in the IRI group were significantly higher than in the control group (3.17 ± 0.21 and 0.28 ± 0.03 vs 654.2 ± 3.6 pg/mL and 147.4 ± 1.1 pg/mL; t value = 4.11 and 4.29 for each; P <.01). Compared with the IRI group they were greatly decreased after anti-CD14 antibody treatment: 2.14 ± 0.17 vs 3.17 ± 0.21, 298.7 ± 1.8 pg/mL vs 654.2 ± 3.6 pg/mL (t value = 2.52 and 2.92 for each; P <.05). They were still significantly higher than the control group (t values of 3.01 and 3.27 for each; P <.01). Conclusion: IRI up-regulated CD14 and TLR4 gene expression in KCs, and subsequently activated NF-κβ to produce cytokines.
机译:目的:本研究的目的是研究库普弗细胞(KCs)中CD14和Toll样受体4(TLR4)在大鼠肝移植物中的缺血再灌注损伤(IRI)中的作用。方法:从对照组,IRI和IRI加抗CD14抗体组获得分离的KC。我们测量了信使RNA(mRNA)和脂多糖受体CD14和TLR4的蛋白表达,核因子κB(NF-κβ)活性以及TNF-α水平。结果:IRI中CD14和TLR4的mRNA和蛋白表达显着高于对照组,通过流式细胞术和Western blot检测CD14和TLR4的蛋白表达。 IRI组的NF-κβ活性和肿瘤坏死因子-α水平显着高于对照组(3.17±0.21和0.28±0.03 vs 654.2±3.6 pg / mL和147.4±1.1 pg / mL; t值= 4.11并分别为4.29; P <.01)。与IRI组相比,抗CD14抗体治疗后它们显着降低:2.14±0.17 vs 3.17±0.21、298.7±1.8 pg / mL vs 654.2±3.6 pg / mL(t值分别为2.52和2.92; P <。 05)。它们仍显着高于对照组(t值分别为3.01和3.27; P <.01)。结论:IRI上调了KCs中CD14和TLR4基因的表达,并随后激活NF-κB产生细胞因子。

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