Wang Jinxin, Li Xiaomin, Bello Babatunde Kazeem, Yu Guili, Yang Qiankun, Yang Haitao, Zhang Wei, Wang Lei, Dong Jingquan, Liu Gang, Zhao Panpan
Jiangsu Institute of Marine Resources Develepment, Co-Innovation Center of Jiangsu Marine Bio-industry Technology, Jiangsu Key Laboratory of Marine Pharmaceutical Compound Screening, Jiangsu Key Laboratory of Marine Bioresources and Environment, Jiangsu Ocean University, Lianyungang 222005, China.
Department of Oncology, The Second People's Hospital of Lianyungang City, Lianyungang, 222002, China.
Microb Pathog. 2022 Jan;162:105219. doi: 10.1016/j.micpath.2021.105219. Epub 2021 Sep 30.
Vibrio alginolyticus is an important zoonotic marine pathogenic bacterium. Previous studies on the mechanism of innate immune against V. alginolyticus infection have been limited to aquatic animals, however, how V. alginolyticus activates mammalian immune cells has not been fully clarified. Here, ELISA combined RT-qPCR assays were used to detect the secretion and transcription level of pro-inflammatory cytokines and TLRs during V. alginolyticus infection of mice peritoneal macrophages (PMϕs). Western blotting was used to explore the phosphorylation levels of p38, JNK, ERK, AKT and NF-κB protein. Immunofluorescence assay was used to determine the location of NF-κB protein. Inhibition assay was used to study the role of up-regulated TLR in activated signaling pathways and the role of these pathways in the release of pro-inflammatory cytokines. Our data showed that V. alginolyticus can up-regulate the expression levels of IL-1β, IL-6, IL-12 and TNF-α in PMϕs. In addition, V. alginolyticus stimulation activated the phosphorylation of p38, JNK and ERK were TLR2 heterodimers-dependent, whereas inhibitors of SB203580 (p38), SCH772984 (ERK) and SP600125 (JNK) significantly reduced IL-1β, IL-6, IL-12 and TNF-α production. We further revealed that V. alginolyticus activated the signaling pathways of AKT via TLR2 heterodimers. The inhibitor of MK-2206 2HCl (AKT) negatively regulated the IL-1β, IL-6 and TNF-α release levels. Moreover, V. alginolyticus infection of PMϕs resulted in TLR2 heterodimers-mediated activation of NF-κB and induced translocation of phosphorylated NF-κB protein from the cytoplasm into the nucleus via IκBα degradation. V. alginolyticus induced IL-1β, IL-6, IL-12 and TNF-α release were blocked by the specific NF-κB inhibitor, BAY 11-7082. Taken together, our results suggested that activation of the TLR2 heterodimers-mediated downstream signaling pathways NF-κB, MAPK and AKT is responsible for inflammatory response during Vibrio alginolyticus infection in vitro.
溶藻弧菌是一种重要的人畜共患海洋致病菌。以往关于抗溶藻弧菌感染的固有免疫机制的研究仅限于水生动物,然而,溶藻弧菌如何激活哺乳动物免疫细胞尚未完全阐明。在此,采用酶联免疫吸附测定(ELISA)结合逆转录定量聚合酶链反应(RT-qPCR)检测小鼠腹腔巨噬细胞(PMϕs)感染溶藻弧菌期间促炎细胞因子和Toll样受体(TLRs)的分泌及转录水平。利用蛋白质免疫印迹法探究p38、c-Jun氨基末端激酶(JNK)、细胞外信号调节激酶(ERK)、蛋白激酶B(AKT)和核因子κB(NF-κB)蛋白的磷酸化水平。采用免疫荧光测定法确定NF-κB蛋白的定位。利用抑制试验研究上调的TLR在激活信号通路中的作用以及这些通路在促炎细胞因子释放中的作用。我们的数据表明,溶藻弧菌可上调PMϕs中白细胞介素-1β(IL-1β)、IL-6、IL-12和肿瘤坏死因子-α(TNF-α)的表达水平。此外,溶藻弧菌刺激激活p38、JNK和ERK的磷酸化依赖于TLR2异二聚体,而SB203580(p38)、SCH772984(ERK)和SP600125(JNK)抑制剂显著降低IL-1β、IL-6、IL-12和TNF-α的产生。我们进一步揭示,溶藻弧菌通过TLR2异二聚体激活AKT信号通路。MK-2206 2HCl(AKT)抑制剂负向调节IL-1β、IL-6和TNF-α的释放水平。此外,溶藻弧菌感染PMϕs导致TLR2异二聚体介导的NF-κB激活,并通过IκBα降解诱导磷酸化NF-κB蛋白从细胞质转位至细胞核。溶藻弧菌诱导的IL-1β、IL-6、IL-12和TNF-α释放被特异性NF-κB抑制剂BAY 11-7082阻断。综上所述,我们的结果表明,TLR2异二聚体介导的下游信号通路NF-κB、丝裂原活化蛋白激酶(MAPK)和AKT的激活是体外溶藻弧菌感染期间炎症反应的原因。