Su Rigu, Peng Yi-Ping, Deng Zhen, Deng Ya-Ting, Ye Jianq-Qing, Guo Yang, Huang Zi-Kun, Luo Qing, Jiang Hong, Li Jun-Ming
Department of Clinical Laboratory, The First Affiliated Hospital of Nanchang University, Nanchang, China.
Department of Tuberculosis, Jiangxi Chest Hospital, Nanchang, China.
Front Microbiol. 2019 Jul 11;10:1468. doi: 10.3389/fmicb.2019.01468. eCollection 2019.
The roles and characteristics of low-density granulocytes (LDGs) have recently attracted attention; however, the mechanism of the formation of LDGs is yet unclear. In one of our previous studies, the frequency of LDGs was significantly elevated in the peripheral blood of tuberculosis patients, and activation contributed to the generation of LDGs upon infection. However, the underlying molecular mechanisms are yet to be elucidated. In the present study, the release of neutrophil extracellular traps (NETs) and the levels of ROS were regulated before the normal-density granulocytes (NDGs) to be infected with , and the conversion of NDGs to LDGs was monitored subsequently as well. The results showed that tuberculosis-related LDGs spontaneously released high levels of NETs. Promoting the release of NETs led to increase in the conversion of NDGs to LDGs in infection, while inhibiting the release of NETs suppressed this conversion after the infection. The infection significantly increased the ROS levels in neutrophils and the conversion of NDGs to LDGs. Scavenging ROS or blocking the ROS generation of -infected NDGs significantly suppressed the release of NETs and blocked the generation of LDGs. Moreover, inhibiting the formation of NETs without affecting the levels of ROS significantly decreased the conversion of NDGs to LDGs after infection. Overall, this study demonstrated that could induce the generation of LDGs by promoting the release of NET ROS pathway.
低密度粒细胞(LDGs)的作用和特征近来受到关注;然而,LDGs的形成机制尚不清楚。在我们之前的一项研究中,结核病患者外周血中LDGs的频率显著升高,感染时的激活作用促使了LDGs的产生。然而,其潜在的分子机制仍有待阐明。在本研究中,在正常密度粒细胞(NDGs)被感染之前,对中性粒细胞胞外陷阱(NETs)的释放和活性氧(ROS)水平进行调节,随后监测NDGs向LDGs的转化。结果表明,结核病相关的LDGs自发释放高水平的NETs。促进NETs的释放导致感染时NDGs向LDGs的转化增加,而抑制NETs的释放则在感染后抑制了这种转化。感染显著增加了中性粒细胞中的ROS水平以及NDGs向LDGs的转化。清除ROS或阻断感染NDGs的ROS生成显著抑制了NETs的释放并阻断了LDGs的生成。此外,在不影响ROS水平的情况下抑制NETs的形成,在感染后显著降低了NDGs向LDGs的转化。总体而言,本研究表明,可通过促进NET-ROS途径的释放诱导LDGs的产生。