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人RPMI 8226 B细胞中,CpG寡脱氧核苷酸对NF-κB反应性基因表达的CG序列及硫代磷酸酯骨架修饰依赖性激活。

CG sequence- and phosphorothioate backbone modification-dependent activation of the NF-kappaB-responsive gene expression by CpG-oligodeoxynucleotides in human RPMI 8226 B cells.

作者信息

Lee Keun-Wook, Kim Doo-Sik, Kwon Hyung-Joo

机构信息

Department of Biochemistry, College of Science, Yonsei University, Seoul 120-749, South Korea.

出版信息

Mol Immunol. 2004 Aug;41(10):955-64. doi: 10.1016/j.molimm.2004.06.022.

Abstract

Oligodeoxynucleotides containing CpG motifs (CpG-ODNs) have gained attention because of their stimulatory effects on innate immune responses. CpG-ODN 1826 containing two GACGTT motifs is well known to activate the mouse immune cells while CpG-ODN 2006 containing three GTCGTT motifs is optimal for human cells. We have shown that stimulation of the human B cell line RPMI 8226 with CpG-ODN 1826 or 2006 results in the activation of IL-8 promoter and nuclear localization of NF-kappaB in the CG sequence- and phosphorothioate backbone modification-dependent manner. It was also demonstrated that myeloid differentiation protein and tumor necrosis factor receptor-associated factor 6 are involved in the signal transduction pathway triggered by the CpG-ODNs. Furthermore, phosphorothioate-modified CpG-ODN 1826 led to induce the NF-kappaB-responsive inflammatory cytokine gene expression in the cells. Experimental results indicated that the phosphorothioate derivative of CpG-ODN 1826 not only activates the mouse immune cells, but also stimulates NF-kappaB responsive gene expression in the human B cell line.

摘要

含有CpG基序的寡脱氧核苷酸(CpG-ODNs)因其对先天免疫反应的刺激作用而受到关注。含有两个GACGTT基序的CpG-ODN 1826可激活小鼠免疫细胞,而含有三个GTCGTT基序的CpG-ODN 2006对人类细胞最为有效。我们已经表明,用CpG-ODN 1826或2006刺激人B细胞系RPMI 8226会导致IL-8启动子的激活以及NF-κB以CG序列和硫代磷酸酯骨架修饰依赖的方式进行核定位。还证明了髓样分化蛋白和肿瘤坏死因子受体相关因子6参与了由CpG-ODNs触发的信号转导途径。此外,硫代磷酸酯修饰的CpG-ODN 1826导致细胞中NF-κB反应性炎性细胞因子基因表达的诱导。实验结果表明,CpG-ODN 1826的硫代磷酸酯衍生物不仅能激活小鼠免疫细胞,还能刺激人B细胞系中NF-κB反应性基因的表达。

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