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核苷酸结合寡聚化结构域蛋白 2 调控伯克霍尔德菌感染的 RAW 264.7 小鼠巨噬细胞系中细胞因子信号转导抑制因子 3 的表达。

Nucleotide-binding oligomerization domain-containing protein 2 regulates suppressor of cytokine signaling 3 expression in Burkholderia pseudomallei-infected mouse macrophage cell line RAW 264.7.

机构信息

Department of Microbiology, Mahidol University, Bangkok, Thailand.

出版信息

Innate Immun. 2011 Dec;17(6):532-40. doi: 10.1177/1753425910385484. Epub 2010 Nov 18.

Abstract

Burkholderia pseudomallei, a causative agent of melioidosis, is a facultative intracellular Gram-negative bacterium that can survive and multiply inside the macrophages. Toll-like receptors are one class of pattern recognition receptors (PRRs) that have been documented to play significant role in B. pseudomallei infection. In the present study, we investigated a potential role of nucleotide-binding oligomerization domain-containing protein 1 and 2 (NOD1 and NOD2), cytoplasmic pattern recognition receptors, in B. pseudomallei-infected mouse macrophage cell line RAW 264.7. Both live and heat-killed B. pseudomallei were able to up-regulate NOD1 and NOD2 expression in a time-dependent manner. Marked reduction of a negative regulator, suppressor of cytokine signaling 3 (SOCS3), expression was observed only in B. pseudomallei-infected NOD2-depleted macrophages and not in NOD1-depleted macrophages. The decrease in SOCS3 expression also led to an increase in IFN-γ responsiveness as judged by an enhanced STAT-1 phosphorylation on tyrosine 701 in the B. pseudomallei-infected macrophages. Together, these results suggested that, in addition to using other PRRs to evade macrophage defense, B. pseudomallei may also use NOD2 to regulate a negative regulator like SOCS3.

摘要

类鼻疽伯克霍尔德菌是类鼻疽病的病原体,是一种兼性细胞内革兰氏阴性细菌,能够在巨噬细胞内生存和繁殖。Toll 样受体是一类模式识别受体 (PRRs),已被证明在类鼻疽伯克霍尔德菌感染中发挥重要作用。在本研究中,我们研究了胞质模式识别受体核苷酸结合寡聚结构域蛋白 1 和 2 (NOD1 和 NOD2) 在类鼻疽伯克霍尔德菌感染的 RAW 264.7 巨噬细胞系中的潜在作用。活的和热杀死的类鼻疽伯克霍尔德菌均能以时间依赖性方式上调 NOD1 和 NOD2 的表达。仅在 NOD2 耗尽的巨噬细胞中观察到负调节剂细胞因子信号转导抑制因子 3 (SOCS3) 的表达明显减少,而在 NOD1 耗尽的巨噬细胞中则没有。SOCS3 表达的减少也导致 IFN-γ 反应性增加,这可以通过 B. pseudomallei 感染的巨噬细胞中 STAT-1 酪氨酸 701 的磷酸化增强来判断。总之,这些结果表明,除了使用其他 PRRs 逃避巨噬细胞防御外,类鼻疽伯克霍尔德菌还可能利用 NOD2 来调节 SOCS3 等负调节剂。

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