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禽类特异性 TLR 及其下游效应对鸡巨噬细胞中 CpG 诱导的反应。

Avian-specific TLRs and downstream effector responses to CpG-induction in chicken macrophages.

机构信息

Department of Animal Science, Iowa State University, Ames, IA 50011, USA.

出版信息

Dev Comp Immunol. 2011 Mar;35(3):392-8. doi: 10.1016/j.dci.2010.11.012. Epub 2010 Nov 30.

Abstract

Chickens possess toll-like receptor (TLR15), a pattern recognition receptor (PRR) absent in mammals. We characterized the regulation and mechanism of CpG responsiveness via TLRs in chicken macrophage HD11 cells. TLR15 was significantly upregulated after induction with B- and C-type CpG oligonucleotides (ODN), tripalmitoylated lipopeptide (PAM3CSK4), Escherichia coli- and Salmonella enteritidis-derived lipopolysaccharide (LPS). In response to CpG-ODN inhibitor, TLR15 and IL1B were downregulated, but TLR21 was upregulated. IL1B was upregulated with CpG-ODN and downregulated after inhibitor treatment. The results suggest that responsiveness to different types of CpG-ODN in chicken macrophages requires multiple receptors, each with unique variation in expression. We utilized RNA interference (RNAi) technology to examine myeloid differentiation primary response gene (MyD88) dependency of TLR15 and TLR21. HD11 macrophages transfected with multiple MyD88-target siRNAs exhibited 70% decrease in MyD88 mRNA expression. IL1B was upregulated with CpG induction in cells with no reduction of MyD88 mRNA levels, but not in cells with 70% MyD88 reduction. Therefore, induction through TLR15 in response to CpG-ODN operates via the MyD88-dependent pathway in chicken macrophages.

摘要

鸡具有 Toll 样受体 (TLR15),这是一种哺乳动物中不存在的模式识别受体 (PRR)。我们在鸡巨噬细胞 HD11 细胞中对 TLR 介导的 CpG 反应的调节和机制进行了表征。B 型和 C 型 CpG 寡核苷酸 (ODN)、三棕榈酰化脂肽 (PAM3CSK4)、大肠杆菌和肠炎沙门氏菌衍生的脂多糖 (LPS) 诱导后,TLR15 显著上调。TLR15 和 IL1B 在 CpG-ODN 抑制剂处理后下调,但 TLR21 上调。IL1B 随着 CpG-ODN 上调,抑制剂处理后下调。结果表明,鸡巨噬细胞对不同类型 CpG-ODN 的反应需要多种受体,每种受体的表达都有独特的变化。我们利用 RNA 干扰 (RNAi) 技术研究了 TLR15 和 TLR21 对髓样分化初级反应基因 (MyD88) 的依赖性。用多个 MyD88 靶向 siRNA 转染的 HD11 巨噬细胞中,MyD88 mRNA 表达下降 70%。CpG 诱导可使鸡巨噬细胞中的 IL1B 上调,而 MyD88 mRNA 水平无降低,但在 MyD88 降低 70%的细胞中则没有上调。因此,鸡巨噬细胞中 TLR15 对 CpG-ODN 的诱导作用是通过 MyD88 依赖途径发挥作用的。

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