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激活小鼠TLR9的寡脱氧核糖核苷酸的物种特异性最小序列基序。

Species-Specific Minimal Sequence Motif for Oligodeoxyribonucleotides Activating Mouse TLR9.

作者信息

Pohar Jelka, Lainšček Duško, Fukui Ryutaro, Yamamoto Chikako, Miyake Kensuke, Jerala Roman, Benčina Mojca

机构信息

Laboratory of Biotechnology, National Institute of Chemistry, SI-1000 Ljubljana, Slovenia;

Division of Innate Immunity, Department of Microbiology and Immunology, Institute of Medical Science, University of Tokyo, Tokyo 108-8639, Japan;

出版信息

J Immunol. 2015 Nov 1;195(9):4396-405. doi: 10.4049/jimmunol.1500600. Epub 2015 Sep 28.

Abstract

Synthetic oligodeoxyribonucleotides (ODNs) containing unmethylated CpG recapitulate the activation of TLR9 by microbial DNA. ODNs are potent stimulators of the immune response in cells expressing TLR9. Despite extensive use of mice as experimental animals in basic and applied immunological research, the key sequence determinants that govern the activation of mouse TLR9 by ODNs have not been well defined. We performed a systematic investigation of the sequence motif of B class phosphodiester ODNs to identify the sequence properties that govern mouse TLR9 activation. In contrast to ODNs activating human TLR9, where the minimal sequence motif for the receptor activation comprises a pair of closely positioned CpGs we found that the mouse TLR9 requires a single CpG positioned 4-6 nt from the 5'-end. Activation is augmented by a 5'TCC sequence one to three nucleotides from the CG. The distance of the CG dinucleotide of four to six nucleotides from the 5'-end and the ODN's length fine-tunes activation of mouse macrophages. Length of the ODN <23 and >29 nt decreases activation of dendritic cells. The ODNs with minimal sequence induce Th1-type cytokine synthesis in dendritic cells and confirm the expression of cell surface markers in B cells. Identification of the minimal sequence provides an insight into the sequence selectivity of mouse TLR9 and points to the differences in the receptor selectivity between species probably as a result of differences in the receptor binding sites.

摘要

含有未甲基化CpG的合成寡脱氧核糖核苷酸(ODN)可模拟微生物DNA对TLR9的激活作用。ODN是表达TLR9的细胞中免疫反应的有效刺激物。尽管在基础和应用免疫学研究中广泛使用小鼠作为实验动物,但尚未明确决定ODN激活小鼠TLR9的关键序列决定因素。我们对B类磷酸二酯ODN的序列基序进行了系统研究,以确定决定小鼠TLR9激活的序列特性。与激活人TLR9的ODN不同,人TLR9激活的最小序列基序包含一对紧密相邻的CpG,我们发现小鼠TLR9需要一个位于5'端4-6个核苷酸处的单个CpG。从CG起1至3个核苷酸处的5'TCC序列可增强激活作用。5'端4至6个核苷酸处的CG二核苷酸的距离和ODN的长度可微调小鼠巨噬细胞的激活。ODN长度<23和>29个核苷酸会降低树突状细胞的激活。具有最小序列的ODN可诱导树突状细胞中Th1型细胞因子的合成,并证实B细胞中细胞表面标志物的表达。最小序列的鉴定为深入了解小鼠TLR9的序列选择性提供了思路,并指出了物种间受体选择性的差异可能是由于受体结合位点的差异所致。

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