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粪肠球菌菌株EC-12的核酸是有效的Toll样受体7和9配体,可诱导小鼠脾细胞和小鼠巨噬细胞系J774.1产生白细胞介素-12。

Nucleic acids of Enterococcus faecalis strain EC-12 are potent Toll-like receptor 7 and 9 ligands inducing interleukin-12 production from murine splenocytes and murine macrophage cell line J774.1.

作者信息

Inoue Ryo, Nagino Takayuki, Hoshino Go, Ushida Kazunari

机构信息

Laboratory of Animal Science, Kyoto Prefectural University, Shimogamo, Kyoto, Japan.

出版信息

FEMS Immunol Med Microbiol. 2011 Feb;61(1):94-102. doi: 10.1111/j.1574-695X.2010.00752.x. Epub 2010 Nov 12.

Abstract

In experiment 1 of this study, the interleukin-12 (IL-12)-inducing ability of six Enterococcus strains was evaluated in comparison with that of five Lactobacillus strains using murine splenocytes. At the same time, the involvement of Toll-like receptor (TLR) ligands in IL-12-inducing ability was assessed using splenocytes from TLR2-, TLR4- and MyD88-deficient mice. Most Enterococcus strains, especially Enterococcus faecalis strain EC-12, exerted higher IL-12-inducing ability compared with the Lactobacillus strains evaluated. Almost the same amount of IL-12 protein was produced by all lactic acid bacteria strains in splenocytes from TLR2- and TLR4-deficient mice, whereas splenocytes from MyD88-deficient mice showed no IL-12 production against all bacteria evaluated. In experiment 2, the role of TLR7, 8 and 9 ligands of E. faecalis strain EC-12 in the induction of IL-12 production was evaluated using murine macrophage cell line J774.1. A drastic decrease in IL-12-inducing ability was observed when heat-killed E. faecalis strain EC-12 was treated with nuclease, particularly RNase. In addition, less than one-tenth of IL-12 was produced by heat-killed E. faecalis strain EC-12 when both TLR7 and 9 were antagonized. These facts indicate that the nucleic acids of E. faecalis strain EC-12, particularly its RNA, are the potent TLR7 and 9 ligands that induce IL-12 production from antigen-presenting cells.

摘要

在本研究的实验1中,使用小鼠脾细胞评估了6株肠球菌菌株诱导白细胞介素-12(IL-12)的能力,并与5株乳酸杆菌菌株进行了比较。同时,使用来自Toll样受体(TLR)2、TLR4和髓样分化因子88(MyD88)缺陷小鼠的脾细胞评估了TLR配体对IL-12诱导能力的影响。与所评估的乳酸杆菌菌株相比,大多数肠球菌菌株,尤其是粪肠球菌菌株EC-12,具有更高的IL-12诱导能力。在来自TLR2和TLR4缺陷小鼠的脾细胞中,所有乳酸菌菌株产生的IL-12蛋白量几乎相同,而来自MyD88缺陷小鼠的脾细胞对所有评估的细菌均未显示出IL-12产生。在实验2中,使用小鼠巨噬细胞系J774.1评估了粪肠球菌菌株EC-12的TLR7、8和9配体在诱导IL-12产生中的作用。当用核酸酶,特别是核糖核酸酶处理热灭活的粪肠球菌菌株EC-12时,观察到IL-12诱导能力急剧下降。此外,当TLR7和9均被拮抗时,热灭活的粪肠球菌菌株EC-12产生的IL-12不到十分之一。这些事实表明,粪肠球菌菌株EC-12的核酸,尤其是其RNA,是诱导抗原呈递细胞产生IL-12的有效的TLR7和9配体。

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