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连翘提取物对小鼠腹腔巨噬细胞体外吞噬和NO释放的影响
引用本文:尹乐乐,曾耀英,侯会娜.连翘提取物对小鼠腹腔巨噬细胞体外吞噬和NO释放的影响[J].细胞与分子免疫学杂志,2008,24(6):557-560.
作者姓名:尹乐乐  曾耀英  侯会娜
作者单位:暨南大学生命科学技术学院组织移植与免疫研究中心,广东,广州,510632
基金项目:国家重点基础研究发展计划(973计划) , 广东省广州市科技局科技攻关项目
摘    要:目的:分析连翘(FS)对小鼠腹腔巨噬细胞的体外吞噬和体外NO释放的影响.方法:无菌收集小鼠腹腔巨噬细胞和羧基荧光素乙酰乙酸琥珀酰亚胺酯(CFDA-SE)标记大肠杆菌DH5α,短期培养3 h后流式细胞术(FCM)分析FS对腹腔巨噬细胞体外吞噬的影响.用LPS体外刺激活化腹腔巨噬细胞,Griess Reagent试剂盒检测并分析FS对巨噬细胞体外释放NO的影响.结果:FCM分析显示,终浓度为40、80、160 mg/L的FS对小鼠腹腔巨噬细胞体外吞噬具有明显的促进作用(P<0.05).不同终质量浓度的FS对LPS诱导小鼠腹腔巨噬细胞体外NO的释放均有抑制作用(P<0.05).结论:FS可以促进小鼠腹腔巨噬细胞的体外吞噬和抑制NO体外的释放.

关 键 词:连翘提取物  腹腔巨噬细胞  吞噬  NO释放  连翘提取物  小鼠腹腔巨噬细胞  细胞体外  影响  in  vitro  production  peritoneal  macrophages  phagocytosis  extract  抑制作用  质量浓度  显示  结果  体外释放  检测  试剂盒  Reagent  活化  外刺激  流式细胞术
文章编号:1007-8738(2008)06-0557-04
修稿时间:2007年9月7日

Effect of forsythia suspense extract on phagocytosis of peritoneal macrophages and NO production in vitro
YIN Le-le,ZENG Yao-ying,HOU Hui-na.Effect of forsythia suspense extract on phagocytosis of peritoneal macrophages and NO production in vitro[J].Journal of Cellular and Molecular Immunology,2008,24(6):557-560.
Authors:YIN Le-le  ZENG Yao-ying  HOU Hui-na
Institution:Institute of Tissue Transplantation and Immunology, College of Life Science and Technology, Jinan University, Guangzhou 510632, China.
Abstract:AIM: To investigate the effect of forsythia suspensa (FS) extract on phagocytosis of peritoneal macrophages and NO production in vitro. METHODS: The peritoneal macrophagess were isolated from BALB/c mice. After stained with CFDA-SE, the DH5alpha were co-cultured with peritoneal macrophagess for 3 h. The effect of FS extract on cyto-phagocytesis in vitro was analyzed by flow cytometry. The peritoneal macrophages were stimulated and activated by LPS in vitro. The effect of FS extract on NO production of the peritoneal macrophages in vitro was measured by NO assay kit. RESULTS: FCM analysis showed that FS extract significantly promoted the phagocytosis of peritoneal macrophages at the final concentration of 40, 80, 160 mg/L, respectively (P<0.05). It also decreased the production of NO at different concentration induced by LPS (P<0.05). CONCLUSION: FS extract can promote phagocytosis of peritoneal macrophages and inhibit NO production in vitro.
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