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山东大学学报(医学版)

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黄芪在同种移植排斥中对CD4+CD25+T细胞Foxp3的影响

李春霞,侯桂华,宋静,张超,梁婷,郑永先   

  1. 山东大学实验核医学研究所, 山东 济南 250012
  • 收稿日期:2006-01-10 修回日期:1900-01-01 出版日期:2006-08-24 发布日期:2006-08-24
  • 通讯作者: 李春霞

LI Chunxia, HOU Gui-hua,SONG Jing, ZHANG Chao, LIANG Ting, ZHENG Yong-xian   

  1. 黄芪注射液;同种异体移植;T淋巴细胞,调节;免疫耐受;小鼠,近交BALB C
  • Received:2006-01-10 Revised:1900-01-01 Online:2006-08-24 Published:2006-08-24
  • Contact: LI Chunxia

摘要: 探讨黄芪(AST)在同种移植排斥中对CD4+CD25+T细胞动态变化及Foxp3表达的影响。方法:C57BL/6和BALB/c小鼠分别为供体和受体,建立皮肤移植模型。对照组:术后注射生理盐水;AST组:术后给予黄芪注射液;AST+脾细胞(SP)组:术前输注供体鼠脾细胞,术后给予黄芪注射液,CsA+SP组:术前输注供体鼠脾细胞,术后给予环孢素A(CsA)。术后逐日观察移植皮肤存活情况及小鼠一般状况;免疫荧光染色流式细胞术检测脾组织中CD4+CD25+T细胞动态变化;RTPCR检测Foxp3mRNA表达情况。结果:与对照组相比,AST组、AST+SP组、CsA+SP组移植皮片存活时间明显延长(P<0.05),移植后14?d,CD4+CD25+T细胞数量及Foxp3的相对表达量显著增多(P<0.05)。结论:黄芪体内用药可延长同种移植物的存活时间,上调CD4+CD25+T细胞及Foxp3的活性。

Abstract: [ABSTRACT]Objective: To study the effect of Astragalus (AST) on CD4+CD25+ T cells and Foxp3 after allotransplantation. Methods: Skin of C57BL/6 mice were transplanted to BALB/c mice. Control group: Sodium Chloride were given, group AST: Astragalus injection were given, group AST+spleen cells (SP): spleen cells of donor mice were given before transplantation and Astragalus injection were given after transplantation, group CsA+SP: spleen cells of donor mice were given before transplantation and Ciclosporin(CsA) were given after transplantation. Survival condition of grafted skin and general condition of mice were observed daily; Numbers of CD4+CD25+ T cells were examined by immunofluorescence staining and flow cytometry; The mRNA expression of Foxp3 was tested by RTPCR. Results: Compared with group Control, allograft survival time of group AST、 AST+SP、 CsA+SP prolonged significantly(P<0.05), The level of CD4+CD25+ T cells and the expression of Foxp3 mRNA increased obviously on 14th day after transplantation(P<0.05). Conclusion: Using Astragalus in vivo can prolong graft survival time obviously and upregulate the level of CD4+CD25+ T cells and the expression of Foxp3.

Key words: Astragalus, Allogeneic transplantation, TLymphocytes, Regulatory, Immune tolerance, Mice, Inbred BALB

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