摘要
目的:探讨细粒棘球蚴通过调控巨噬细胞STAT6的表达介导其极化的机制。方法:使用细粒棘球蚴囊液(EgCF)处理巨噬细胞系Raw264.7,以未加EgCF组作为对照组,qRT-PCR、ELISA、流式细胞术等实验检测M1、M2相关因子的表达水平,研究细粒棘球蚴对巨噬细胞极化的影响;使用EgCF处理巨噬细胞,并在实验组加入信号转导和转录激活因子6(STAT6)抑制剂,以未加抑制剂组及DMSO组作为对照组,qRT-PCR、流式细胞术等实验检测STAT6、M1、M2相关因子的表达水平,研究细粒棘球蚴通过调控巨噬细胞STAT6的表达,介导巨噬细胞极化的机制。结果:EgCF促进STAT6和M2相关因子的表达(P<0.05),抑制M1相关因子的表达(P<0.05)。STAT6抑制剂可抑制Raw264.7细胞中STAT6和M2相关因子表达,并上调M1相关因子表达。结论:EgCF通过促进STAT6的表达介导巨噬细胞向M2型极化。
Objective:To explore the mechanism of macrophage polarization mediated by Echinococcus granulosus through regulating STAT6 expression in macrophage.Methods:Echinococcus granulosuscyst fluid(EgCF)was used to treat macrophages Raw264.7,the group without EgCF was used as a comparison control group.qRT-PCR,ELISA and flow cytometry were used to detect M1 and M2-related factors in macrophages to study the effect of Echinococcus granulosus on macrophage polarization;macrophages were treated with EgCF,and an inhibitor of signal transducer and activator of transcription6(STAT6)was added to experimental group,while non-inhibitor group and DMSO group were used as control groups.qRT-PCR and flow cytometry were used to detect expressions of STAT6,M1 and M2-related factors to investigate the mechanism by which Echinococcus granulosus mediates polarization of macrophages by regulating expression of STAT6 in macrophages.Results:EgCF promoted expressions of STAT6 and M2-related factors(P<0.05)and inhibited expressions of M1-related factors(P<0.05).STAT6 inhibitor inhibited expressions of STAT6 and M2-related factors and up-regulated expressions of M1-related factors in Raw264.7 cells.Conclusion:EgCF mediates macrophage polarization towards M2 phenotype by promoting STAT6 expression.
作者
冯叶叶
许军英
逯君霞
侯隽
王良海
吴向未
陈雪玲(指导)
FENG Yeye;XU Junying;LU Junxia;HOU Jun;WANG Lianghai;WU Xiangwei;CHEN Xueling(School of Medicine,Shihezi University,Shihezi 832002,China)
出处
《中国免疫学杂志》
CAS
CSCD
北大核心
2022年第10期1158-1163,共6页
Chinese Journal of Immunology
基金
中国医学科学院中央级公益性科研院所基本科研业务费专项资金(2020-PT330-003)
国自然地区科学基金项目(82060297)
兵团财政科技计划项目区域创新引导计划(2021BB006)
石河子大学校级科研项目(ZZZC202132)资助。