Akaike Takaaki, Okamoto Tatsuya, Zaki Md Hasan, Fujii Shigemoto, Sawa Tomohiro
Department of Microbiology, Graduate School of Medical Sciences, Kumamoto University, Kumamoto, Japan.
Nihon Hansenbyo Gakkai Zasshi. 2009 Feb;78(1):41-7. doi: 10.5025/hansen.78.41.
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.
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。