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细菌的CpG-DNA和脂多糖在不同的细胞区室激活Toll样受体。

Bacterial CpG-DNA and lipopolysaccharides activate Toll-like receptors at distinct cellular compartments.

作者信息

Ahmad-Nejad Parviz, Häcker Hans, Rutz Mark, Bauer Stefan, Vabulas Ramunas M, Wagner Hermann

机构信息

Institute of Medical Microbiology, Immunology and Hygiene, Technische Universität München, Munich, Germany.

出版信息

Eur J Immunol. 2002 Jul;32(7):1958-68. doi: 10.1002/1521-4141(200207)32:7<1958::AID-IMMU1958>3.0.CO;2-U.

Abstract

Recognition by innate immune cells of the pathogen associated molecular patterns (PAMP) lipopolysaccharide (LPS) from Gram-negative bacteria and bacterial CpG-DNA depends on Toll-like receptor4 (TLR4) and TLR9, respectively. To define differences in the response to these distinct PAMP we compared a key intracellular event, namely recruitment of myeloid differentiation marker 88 (MyD88) to the respective PAMP-initiated TLR signaling. Using MyD88-GFP fusion protein expressing macrophages we demonstrate that LPS and CpG-DNA trigger signaling from two different cellular locations: theformer at the cell membrane and the latter at the lysosomal compartment. While LPS does not require endocytosis to functionally associate with the membrane expressed TLR4/MD2 complex, internalization and endosomal maturation is conditional for CpG-DNA to activate TLR9. In support of these data TLR9 is not localized at the cell surface, but intracellularily. These data stress the need to characterize individual TLR at the very beginning of signal initiation in order to understand their diverse biological functions.

摘要

天然免疫细胞对革兰氏阴性菌的病原体相关分子模式(PAMP)脂多糖(LPS)和细菌CpG-DNA的识别分别依赖于Toll样受体4(TLR4)和TLR9。为了确定对这些不同PAMP反应的差异,我们比较了一个关键的细胞内事件,即髓样分化标志物88(MyD88)向各自由PAMP启动的TLR信号转导的募集。使用表达MyD88-GFP融合蛋白的巨噬细胞,我们证明LPS和CpG-DNA从两个不同的细胞位置触发信号转导:前者在细胞膜,后者在溶酶体区室。虽然LPS在功能上与膜表达的TLR4/MD2复合物结合不需要内吞作用,但内化和内体成熟是CpG-DNA激活TLR9的条件。支持这些数据的是,TLR9并不定位于细胞表面,而是定位于细胞内。这些数据强调了在信号启动的最初阶段就对单个TLR进行表征的必要性,以便了解它们多样的生物学功能。

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