Zhou Weiqiang, Duan Zhiwen, Yang Biao, Xiao Chunling
Key Laboratory of Environmental Pollution and Microecology of Liaoning Province, Shenyang Medical College, No.146 North Huanghe St, Huanggu Dis, Shenyang City, Liaoning Pro, P. R. China110034.
Department of Toxicology, School of Public Health, Shenyang Medical College, No.146 North Huanghe St, Huanggu Dis, Shenyang City, Liaoning Pro, P. R. China110034.
Open Med (Wars). 2017 Sep 25;12:299-307. doi: 10.1515/med-2017-0044. eCollection 2017.
PA-MSHA and BPIFB1 play especially important roles in triggering innate immune responses by inducing production of pro- or anti-inflammatory cytokines in the oral cavity and upper airway. We found that PA-MSHA had a strong ability to activate pro-inflammatory cytokines such as IL-1β, IL-6 and TNF-α. However, BPIFB1 alone did not express a directly inductive effect. With incubation of PA-MSHA and BPIFB1, the combination can activate the CD14/TLR4/MyD88 complex and induce secretion of subsequent downstream cytokines. We used a proteome profiler antibody array to evaluate the phosphokinases status with PA-MSHA and BPIFB1 treatment. The results showed that the activation of MAPK, STAT, and PI-3K pathways is involved in PA-MSHA-BPIFB1 treatment, and that the related pathways control the secretion of targeting cytokines in the downstream. When we assessed the content changes of cytokines, we found that PA-MSHA-BPIFB1 treatment increased the production of pro-inflammatory cytokines in the early phase of treatment and induced the increase of IL-4 in the late phase. Our observations suggest that PA-MSHA-BPIFB1 stimulates the release of pro-inflammatory cytokines, and thereby initiates the innate immune system against inflammation. Meanwhile, the gradual release of anti-inflammatory cytokine IL-4 by PA-MSHA-BPIFB1 can also regulate the degree of inflammatory response; thus the host can effectively resist the environmental risks, but also manipulate inflammatory response in an appropriate and adjustable manner.
PA-MSHA和BPIFB1通过诱导口腔和上呼吸道中促炎或抗炎细胞因子的产生,在触发先天免疫反应中发挥着尤为重要的作用。我们发现PA-MSHA具有强大的激活促炎细胞因子如IL-1β、IL-6和TNF-α的能力。然而,单独的BPIFB1并未表现出直接的诱导作用。随着PA-MSHA和BPIFB1的共同孵育,二者组合可激活CD14/TLR4/MyD88复合物并诱导后续下游细胞因子的分泌。我们使用蛋白质组分析抗体阵列来评估PA-MSHA和BPIFB1处理后的磷酸激酶状态。结果表明,MAPK、STAT和PI-3K途径的激活参与了PA-MSHA-BPIFB1处理,并且相关途径控制下游靶向细胞因子的分泌。当我们评估细胞因子的含量变化时,发现PA-MSHA-BPIFB1处理在处理早期增加了促炎细胞因子的产生,并在后期诱导了IL-4的增加。我们的观察结果表明,PA-MSHA-BPIFB1刺激促炎细胞因子的释放,从而启动针对炎症的先天免疫系统。同时,PA-MSHA-BPIFB1逐渐释放抗炎细胞因子IL-4也可调节炎症反应的程度;因此宿主既能有效抵抗环境风险,又能以适当且可调节的方式控制炎症反应。