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Events associated with phagocytolytic activity of PMN cells

Reactome ID: R-HSA-8941413

中文名称

Th17细胞分化

通路描述

产生IL-17的辅助T细胞(Th17)是CD4+ T细胞的一个亚群,参与上皮细胞和中性粒细胞介导的针对外源微生物的免疫反应,以及自身免疫病的发病机制。体内Th17分化需要抗原呈递和共刺激,以及抗原呈递细胞(APCs)的激活以产生TGF-β、IL-6、IL-1、IL-23和IL-21。这种初始激活导致CD4+ T细胞中STAT3、ROR(γ)t和其他转录因子被激活并上调,这些因子结合到IL-17、IL-21和IL-22基因的上游启动子区域,诱导IL-17、IL-21和IL-22的表达。相比之下,Th17细胞的分化和其IL-17表达受到IL-2、Th2细胞因子IL-4、IL-27和Th1细胞因子IFN-γ的负向调节,分别通过STAT5、STAT6和STAT1的激活实现。类固醇酸和IL-2与TGF-β的组合上调Foxp3,从而下调包括IL-17和IL-21在内的细胞因子。抑制Th17分化可能作为一种保护策略,用于“微调”IL-17的表达,使其不会引起过度的炎症。因此,Th细胞的平衡分化对于免疫和宿主保护至关重要。
英文描述
Events associated with phagocytolytic activity of PMN cells When neutrophils engulf bacteria they enclose them in small vacuoles (phagosomes) into which superoxide is released by activated NADPH oxidase (NOX2) on the internalized neutrophil membrane. The directional nature of NOX2 activity creates a charge imbalance that must be counteracted to prevent depolarization of the membrane and the shutdown of activity (Winterbourn CC et al. 2016). Also, protons are produced in the cytosol and consumed in the external compartment (for example, the phagosome) through the dismutation of superoxide. Both situations are largely overcome by a balancing flow of protons transported by voltage-gated proton channels, primarily VSOP/HV1, which are activated in parallel with the oxidase (Demaurex N & El Chemaly A 2010; El Chemaly A et al. 2010; Petheo GL et al. 2010; Kovacs I et al. 2014; Henderson LM et al. 1987, 1988). The pH of the phagosome is regulated by these activities. In contrast to the phagosomes of macrophages, in which pH drops following particle ingestion, neutrophil phagosomes remain alkaline during the period that the oxidase is active. Until recently, their pH has been accepted to lie between 7.5 and 8. However, in a 2015 study using a probe that is more sensitive at higher pH, an average pH closer to 9 was measured in individual phagosomes (Levine AP et al. 2015).The superoxide dismutates to hydrogen peroxide, which is used by myeloperoxidase (MPO) to generate other oxidants, including the highly microbicidal species such as hypochlorous acid (Winterbourn CC et al. 2013, 2016).

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