Naffah de Souza Cristiane, Breda Leandro C D, Khan Meraj A, de Almeida Sandro Rogério, Câmara Niels Olsen Saraiva, Sweezey Neil, Palaniyar Nades
Program in Translational Medicine, Peter Gilgan Centre for Research and Learning, The Hospital for Sick Children, Toronto, ON, Canada.
Department of Laboratory Medicine and Pathobiology, Faculty of Medicine, The University of Toronto, Toronto, ON, Canada.
Front Immunol. 2018 Jan 9;8:1849. doi: 10.3389/fimmu.2017.01849. eCollection 2017.
pH is highly variable in different tissues and affects many enzymatic reactions in neutrophils. In response to calcium ionophores such as A23187 and ionomycin, neutrophils undergo nicotinamide adenine dinucleotide phosphate oxidase (NOX)-independent neutrophil extracellular trap (NET) formation (NETosis). However, how pH influences calcium-dependent Nox-independent NET formation is not well understood. We hypothesized that increasing pH promotes Nox-independent NET formation by promoting calcium influx, mitochondrial reactive oxygen species (mROS) generation, histone citrullination, and histone cleavage. Here, we show that stimulating human neutrophils isolated from peripheral blood with calcium ionophore A23187 or ionomycin in the media with increasing extracellular pH (6.6, 6.8, 7.0, 7.2, 7.4, 7.8) drastically increases intracellular pH within in 10-20 min. These intracellular pH values are much higher compared to unstimulated cells placed in the media with corresponding pH values. Raising pH slightly drastically increases intracellular calcium concentration in resting and stimulated neutrophils, respectively. Like calcium, mROS generation also increases with increasing pH. An mROS scavenger, MitoTempo, significantly suppresses calcium ionophore-mediated NET formation with a greater effect at higher pH, indicating that mROS production is at least partly responsible for pH-dependent suppression of Nox-independent NETosis. In addition, raising pH increases PAD4 activity as determined by the citrullination of histone (CitH3) and histone cleavage determined by Western blots. The pH-dependent histone cleavage is reproducibly very high during ionomycin-induced NETosis compared to A23187-induced NETosis. Little or no histone cleavage was noted in unstimulated cells, at any pH. Both CitH3 and cleavage of histones facilitate DNA decondensation. Therefore, alkaline pH promotes intracellular calcium influx, mROS generation, PAD4-mediated CitH3 formation, histone 4 cleavage and eventually NET formation. Calcium-mediated NET formation and CitH3 formation are often related to sterile inflammation. Hence, understanding these important mechanistic steps helps to explain how pH regulates NOX-independent NET formation, and modifying pH may help to regulate NET formation during sterile inflammation or potential damage caused by compounds such as ionomycin, secreted by , a group of Gram-positive bacteria well known for producing antibiotics.
pH值在不同组织中变化很大,并影响中性粒细胞中的许多酶促反应。响应于钙离子载体如A23187和离子霉素,中性粒细胞经历烟酰胺腺嘌呤二核苷酸磷酸氧化酶(NOX)非依赖性中性粒细胞胞外陷阱(NET)形成(NETosis)。然而,pH如何影响钙依赖性非NOX依赖性NET形成尚不清楚。我们假设提高pH值通过促进钙内流、线粒体活性氧(mROS)生成、组蛋白瓜氨酸化和组蛋白裂解来促进非NOX依赖性NET形成。在这里,我们表明,在细胞外pH值升高(6.6、6.8、7.0、7.2、7.4、7.8)的培养基中,用钙离子载体A23187或离子霉素刺激从外周血中分离的人中性粒细胞,可在10-20分钟内大幅提高细胞内pH值。与置于具有相应pH值的培养基中的未刺激细胞相比,这些细胞内pH值要高得多。略微提高pH值分别会大幅增加静息和刺激的中性粒细胞中的细胞内钙浓度。与钙一样,mROS的产生也随着pH值的升高而增加。一种mROS清除剂MitoTempo显著抑制钙离子载体介导的NET形成,在较高pH值下效果更明显,表明mROS的产生至少部分负责pH依赖性抑制非NOX依赖性NETosis。此外,通过组蛋白瓜氨酸化(CitH3)测定和蛋白质印迹法测定的组蛋白裂解来确定,提高pH值会增加PAD4活性。与A23187诱导的NETosis相比,在离子霉素诱导的NETosis过程中,pH依赖性组蛋白裂解可重复性地非常高。在任何pH值下,未刺激的细胞中几乎没有或没有观察到组蛋白裂解。CitH3和组蛋白裂解都有助于DNA解聚。因此,碱性pH促进细胞内钙内流、mROS生成、PAD4介导的CitH3形成、组蛋白4裂解并最终促进NET形成。钙介导的NET形成和CitH3形成通常与无菌性炎症有关。因此,了解这些重要的机制步骤有助于解释pH如何调节非NOX依赖性NET形成,并且调节pH值可能有助于在无菌性炎症或由一组以产生抗生素而闻名的革兰氏阳性细菌分泌的离子霉素等化合物引起的潜在损伤期间调节NET形成。