Lin L, Huang S, Zhang F, Li J, Jiang X, Chen S
Department of Laboratory Medicine, School of Medicine, Jiangsu University, Zhenjiang, Jiangsu 212013, China.
National Institute of Parasitic Diseases, Chinese Center for Disease Control and Prevention (Chinese Center for Tropical Diseases Research), National Health Commission Key Laboratory of Parasite and Vector Biology, WHO Collaborating Centre for Tropical Diseases, National Center for International Research on Tropical Diseases, Shanghai 200025, China.
Zhongguo Xue Xi Chong Bing Fang Zhi Za Zhi. 2023 Feb 16;35(1):29-37. doi: 10.16250/j.32.1374.2022194.
To investigate the effect of macrophage migration inhibitory factor (TvMIF) on THP-1 macrophages.
Recombinant TvMIF protein was prokaryotic expressed and purified, and endotoxin was removed after identification. Following exposure to TvMIF at concentrations of 0, 1, 5, 10, 50 and 100 ng/mL, the cytotoxicity of the recombinant TvMIF protein to THP-1 macrophages was tested using cell counting kit (CCK)-8 assay, and the apoptosis of THP-1 macrophages and reactive oxygen species (ROS) were detected using flow cytometry. The relative expression of nucleotide-binding oligomerization domain-like receptor protein 3 , interleukin-1β and genes was quantified using real-time fluorescent quantitative PCR (qPCR) assay, and the expression of caspase-1, NLRP3, gasdermin D (GSDMD), gasdermin D N-terminal (GSDMD-NT) and pro-IL-1β proteins were determined using Western blotting assay.
Sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE) displayed successful expression and purification of the recombinant TvMIF protein with a molecular weight of 15.5 kDa, and the endotoxin activity assay showed the successful removal of endotoxin in the recombinant TvMIF protein (endotoxin concentration < 0.1 EU/mL), which was feasible for the subsequent studies on protein functions. Flow cytometry revealed that the recombinant TvMIF protein at a concentration of 10 ng/mL and less promoted the apoptosis of THP-1 macrophages, and the highest apoptotic rate of THP-1 macrophages was seen following exposure to the recombinant TvMIF protein at a concentration of 5 ng/mL, while the recombinant TvMIF protein at concentrations of 50 and100 ng/mL inhibited the apoptosis of THP-1 macrophages. Exposure to the recombinant TvMIF protein at a concentration 1 ng/mL resulted in increased ROS levels in THP-1 macrophages. qPCR assay quantified significantly elevated and expression in THP-1 macrophages 8 hours post-treatment with the recombinant TvMIF protein at a concentration 1 ng/mL, and Western blotting determined increased caspase-1, NLRP3, pro-IL-1β, GSDMD and GSDMD-NT protein expression in THP-1 macrophages following exposure to the recombinant TvMIF protein at a concentration 1 ng/mL. Pretreatment with MCC950 significantly reduced GSDMD and GSDMD-NT protein expression.
High-concentration recombinant TvMIF protein inhibits macrophage apoptosis, while low-concentration recombinant TvMIF protein activates NLRP3 inflammasome and promotes macrophage pyroptosis.
研究巨噬细胞迁移抑制因子(TvMIF)对THP-1巨噬细胞的影响。
原核表达并纯化重组TvMIF蛋白,鉴定后去除内毒素。将THP-1巨噬细胞分别暴露于浓度为0、1、5、10、50和100 ng/mL的TvMIF中,采用细胞计数试剂盒(CCK)-8法检测重组TvMIF蛋白对THP-1巨噬细胞的细胞毒性,采用流式细胞术检测THP-1巨噬细胞的凋亡情况和活性氧(ROS)水平。采用实时荧光定量PCR(qPCR)法检测核苷酸结合寡聚化结构域样受体蛋白3、白细胞介素-1β等基因的相对表达量,采用蛋白质免疫印迹法检测半胱天冬酶-1、NLRP3、gasdermin D(GSDMD)、gasdermin D N端(GSDMD-NT)和前白细胞介素-1β蛋白的表达。
十二烷基硫酸钠聚丙烯酰胺凝胶电泳(SDS-PAGE)显示成功表达并纯化了分子量为15.5 kDa的重组TvMIF蛋白,内毒素活性检测显示重组TvMIF蛋白中的内毒素已成功去除(内毒素浓度<0.1 EU/mL),这为后续蛋白质功能研究提供了可行性。流式细胞术显示,浓度为10 ng/mL及以下的重组TvMIF蛋白促进了THP-1巨噬细胞的凋亡,在暴露于浓度为5 ng/mL的重组TvMIF蛋白后,THP-1巨噬细胞的凋亡率最高,而浓度为50和100 ng/mL的重组TvMIF蛋白则抑制了THP-1巨噬细胞的凋亡。暴露于浓度为1 ng/mL的重组TvMIF蛋白导致THP-1巨噬细胞中的ROS水平升高。qPCR检测显示,在浓度为1 ng/mL的重组TvMIF蛋白处理8小时后,THP-1巨噬细胞中的相关基因表达显著升高,蛋白质免疫印迹法测定显示,暴露于浓度为1 ng/mL的重组TvMIF蛋白后,THP-1巨噬细胞中的半胱天冬酶-1、NLRP3、前白细胞介素-1β、GSDMD和GSDMD-NT蛋白表达增加。用MCC950预处理可显著降低GSDMD和GSDMD-NT蛋白的表达。
高浓度重组TvMIF蛋白抑制巨噬细胞凋亡,而低浓度重组TvMIF蛋白激活NLRP3炎性小体并促进巨噬细胞焦亡。