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[一氧化氮对细胞内病原体宿主防御的新范式]

[New paradigm of host defense against intracellular pathogens by nitric oxide].

作者信息

Akaike Takaaki, Okamoto Tatsuya, Zaki Md Hasan, Fujii Shigemoto, Sawa Tomohiro

机构信息

Department of Microbiology, Graduate School of Medical Sciences, Kumamoto University, Kumamoto, Japan.

出版信息

Nihon Hansenbyo Gakkai Zasshi. 2009 Feb;78(1):41-7. doi: 10.5025/hansen.78.41.

Abstract

Nitric oxide (NO) produced by inducible NO synthase (iNOS) during infection plays a crucial role in host defense mechanisms, via its antimicrobial and cytoprotective activities. Infection of Salmonella typhimurium in mice induces excessive production of NO, as a host defense response. We found much greater bacterial growth and apoptotic changes in iNOS-deficient (iNOS-/-) mice than in wild-type mice. However, the mechanism of NO-mediated cytoprotection during Salmonella infection remained unclear. An important signaling mechanism induced by NO is heme oxygenase (HO)-1, a significant cytoprotective molecule produced by oxidative stress. Thus, we sought to clarify NO-dependent cytoprotective and antimicrobial host defense, with a particular focus on the signaling mechanism of HO-1 induction. We recently discovered a nitrated cyclic nucleotide, 8-nitroguanosine 3',5'-cyclic monophosphate (8-nitro-cGMP), which is formed via NO possibly with reactive oxygen species. We observed strong immunoreactivity for 8-nitro-cGMP in Salmonella-infected wild-type mouse liver and peritoneal macrophages in culture but not in iNOS-/- mouse liver and macrophages. Moreover, a higher apoptosis was observed in iNOS-/- macrophages compared with wild-type macrophages after Salmonella infection, but the difference was nullified when iNOS-/- cells were treated with 8-nitro-cGMP. Finally, authentic 8-nitro-cGMP induced HO-1 in cultured macrophages infected with Salmonella. The signaling function of 8-nitro-cGMP appears to be mediated by its unique reaction with the sulfhydryl group of cysteine, thus forming a proteinS-cGMP adduct, which is an important mechanism of post-translational modification of proteins called protein S-guanylation. More importantly, we found 8-nitro-cGMP-dependent S-guanylation of Keap1, a regulatory protein of transcription factor Nrf2, which regulates the transcription of HO-1. In this review, we focus on a unique mechanism of NO-mediated host defense via formation of a novel signaling molecule, 8-nitro-cGMP in microbial infections.

摘要

感染期间诱导型一氧化氮合酶(iNOS)产生的一氧化氮(NO)通过其抗菌和细胞保护活性在宿主防御机制中发挥关键作用。小鼠感染鼠伤寒沙门氏菌会诱导过量产生NO,作为一种宿主防御反应。我们发现,与野生型小鼠相比,iNOS缺陷型(iNOS-/-)小鼠体内细菌生长和凋亡变化更为明显。然而,沙门氏菌感染期间NO介导的细胞保护机制仍不清楚。NO诱导的一种重要信号机制是血红素加氧酶(HO)-1,它是由氧化应激产生的一种重要的细胞保护分子。因此,我们试图阐明NO依赖性的细胞保护和抗菌宿主防御,特别关注HO-1诱导的信号机制。我们最近发现了一种硝化环核苷酸,8-硝基鸟苷3',5'-环磷酸(8-硝基-cGMP),它可能是由NO与活性氧共同形成的。我们观察到,在感染沙门氏菌的野生型小鼠肝脏和培养的腹腔巨噬细胞中,8-硝基-cGMP具有强烈的免疫反应性,而在iNOS-/-小鼠肝脏和巨噬细胞中则没有。此外,沙门氏菌感染后,iNOS-/-巨噬细胞中的凋亡率高于野生型巨噬细胞,但在用8-硝基-cGMP处理iNOS-/-细胞后,这种差异消失了。最后,在感染沙门氏菌的培养巨噬细胞中,纯的8-硝基-cGMP诱导了HO-1的产生。8-硝基-cGMP的信号功能似乎是通过其与半胱氨酸巯基的独特反应介导的,从而形成一种蛋白质-S-cGMP加合物,这是一种称为蛋白质S-鸟苷酸化的蛋白质翻译后修饰的重要机制。更重要的是,我们发现了转录因子Nrf2的调节蛋白Keap1的8-硝基-cGMP依赖性S-鸟苷酸化,Nrf2可调节HO-1的转录。在这篇综述中,我们重点关注NO通过在微生物感染中形成一种新型信号分子8-硝基-cGMP介导宿主防御的独特机制。

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