中国免疫学杂志
中國免疫學雜誌
중국면역학잡지
CHINESE JOURNAL OF IMMUNOLOGY
2015年
1期
56-60
,共5页
罗进芳%朱瑞丽%易浪%董燕%王培训
囉進芳%硃瑞麗%易浪%董燕%王培訓
라진방%주서려%역랑%동연%왕배훈
青藤碱%脂多糖%白介素4%巨噬细胞极化%M1/M2亚型
青籐堿%脂多糖%白介素4%巨噬細胞極化%M1/M2亞型
청등감%지다당%백개소4%거서세포겁화%M1/M2아형
Sinomenine%Lipopolysaccharide%Interleukin-4%Macrophage polarization%M1/M2 phenotype
目的:探讨青藤碱(Sinomenine,SIN)对脂多糖(LPS)以及白细胞介素4(IL-4)诱导的RAW264.7细胞向M1、M2型极化的影响。方法:以LPS刺激RAW264.7细胞诱导M1型极化,IL-4刺激RAW264.7细胞诱导M2型极化;青藤碱作用于LPS或IL-4诱导的巨噬细胞后:用酶联免疫法( ELISA)检测不同诱导状态下RAW264.7细胞TNF-α和IL-10的分泌量;荧光定量PCR检测与巨噬细胞极化相关的精氨酸酶-1(Arg-1)、一氧化氮合酶(iNOS)、细胞因子信号转导抑制蛋白-2(SOCS2)和细胞因子信号转导抑制蛋白-3(SOCS3)的mRNA表达水平。结果:青藤碱能抑制LPS诱导下细胞TNF-α的分泌量,抑制细胞iNOS和SOCS3的mRNA表达水平的升高。青藤碱能抑制IL-4诱导下细胞IL-10的分泌量和Arg1的mRNA表达水平的升高,对IL-4诱导下细胞SOCS2的mRNA表达水平的升高没有明显影响。结论:青藤碱对LPS诱导下巨噬细胞向M1型极化具有抑制作用;对IL-4诱导下巨噬细胞向M2型极化具有抑制作用。青藤碱对M1/M2亚型的失衡具有调节作用,有利于维持其动态平衡。
目的:探討青籐堿(Sinomenine,SIN)對脂多糖(LPS)以及白細胞介素4(IL-4)誘導的RAW264.7細胞嚮M1、M2型極化的影響。方法:以LPS刺激RAW264.7細胞誘導M1型極化,IL-4刺激RAW264.7細胞誘導M2型極化;青籐堿作用于LPS或IL-4誘導的巨噬細胞後:用酶聯免疫法( ELISA)檢測不同誘導狀態下RAW264.7細胞TNF-α和IL-10的分泌量;熒光定量PCR檢測與巨噬細胞極化相關的精氨痠酶-1(Arg-1)、一氧化氮閤酶(iNOS)、細胞因子信號轉導抑製蛋白-2(SOCS2)和細胞因子信號轉導抑製蛋白-3(SOCS3)的mRNA錶達水平。結果:青籐堿能抑製LPS誘導下細胞TNF-α的分泌量,抑製細胞iNOS和SOCS3的mRNA錶達水平的升高。青籐堿能抑製IL-4誘導下細胞IL-10的分泌量和Arg1的mRNA錶達水平的升高,對IL-4誘導下細胞SOCS2的mRNA錶達水平的升高沒有明顯影響。結論:青籐堿對LPS誘導下巨噬細胞嚮M1型極化具有抑製作用;對IL-4誘導下巨噬細胞嚮M2型極化具有抑製作用。青籐堿對M1/M2亞型的失衡具有調節作用,有利于維持其動態平衡。
목적:탐토청등감(Sinomenine,SIN)대지다당(LPS)이급백세포개소4(IL-4)유도적RAW264.7세포향M1、M2형겁화적영향。방법:이LPS자격RAW264.7세포유도M1형겁화,IL-4자격RAW264.7세포유도M2형겁화;청등감작용우LPS혹IL-4유도적거서세포후:용매련면역법( ELISA)검측불동유도상태하RAW264.7세포TNF-α화IL-10적분비량;형광정량PCR검측여거서세포겁화상관적정안산매-1(Arg-1)、일양화담합매(iNOS)、세포인자신호전도억제단백-2(SOCS2)화세포인자신호전도억제단백-3(SOCS3)적mRNA표체수평。결과:청등감능억제LPS유도하세포TNF-α적분비량,억제세포iNOS화SOCS3적mRNA표체수평적승고。청등감능억제IL-4유도하세포IL-10적분비량화Arg1적mRNA표체수평적승고,대IL-4유도하세포SOCS2적mRNA표체수평적승고몰유명현영향。결론:청등감대LPS유도하거서세포향M1형겁화구유억제작용;대IL-4유도하거서세포향M2형겁화구유억제작용。청등감대M1/M2아형적실형구유조절작용,유리우유지기동태평형。
Objective:To investigate sinomenine (Sinomenine,SIN) effect on RAW264.7 cells polarization to M1 or M2 phenotype induced by lipopolysaccharide (LPS) or interleukin-4 (IL-4) .Methods:RAW264.7 cells were induced to polarize to M1 by LPS ,and to M2 by IL-4.Sinomenine effects on LPS or IL-4 induced macrophages:TNF-αand IL-10 secretion induced by different condition were detected by Enzyme linked immunosorbent assay (ELISA);The expression level of mRNA of Arginase1(Arg-1),Nitric oxide synthase(iNOS),suppressor of cytokine signaling protein-2(SOCS2) and suppressor of cytokine signaling protein-3(SOCS3) of M1/M2 phenotypes were detected by real time PCR respectively.Results:Sinomenine inhibited the increase of TNF-αsecretion,iNOS and SOCS3 mRNA expression level induced by LPS.Sinomenine inhibited the increase of IL-10 secretion and Arg-1 mRNA expression level induced by IL-4,but SOCS2 mRNA expression level was not affected by Sinomenine.Conclusion: Sinomenine can inhibite the macrophage polarization to M1 and M2 induced by LPS and IL-4.Sinomenine plays a regulatory role on imbalance of M1/M2,and is conducive to maintain the dynamic balance.