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Serrate1基因转染对小鼠树突状细胞生物学特性的影响 被引量:3

Effect of Serrate1 gene transfection on biological characteristic of dendritic cells in mice
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摘要 目的探讨Serrate1基因转染对小鼠树突状细胞生物学特性的影响。方法将Serrate1基因体外转染小鼠DCs,经G418筛选后,W estern b lot检测DCsSerrate1的表达,流式细胞仪检测转染后DCs表面共刺激分子的表达,混合淋巴细胞反应观察DCs对T淋巴细胞增殖的影响。结果Serrate1基因转染的树突状细胞Serrate1的表达较未转染组明显增高,转染Serrate1基因的DCs表面CD80、CD86等共刺激分子的表达与对照组比较无明显改变(P>0.05);在混合淋巴细胞反应中,转染DCs对T细胞的增殖有抑制作用,而空载体pcDNA 3.1(+)对照组与未转染组的树突状细胞具有强烈的激发T细胞增殖的能力。结论Serrate1基因转染能在不影响DCs表面共刺激分子表达的情况下显著抑制T细胞活化。 Objective To investigate the effects of Serrate l gene transfer on the biological characteristic of dendritic cells (DCs) in mice. Methods Mice DCs were transfected with pcDNA3.1 ( + ) -Serratel plasmid through Lipofectmine 2000 and the transfected cells were selected by G418. The biological characteristic of transfected DCs were detected by Western blotting, the expression of the costimulatory molecules on the transfected DCs were detected by FACS, and the proliferation of T cells were tested by mixed lymphocyte reaction (MLR). Results The expression of Serratel on the transfected DCs increased significantly than that of non-transfected DCs. There was no difference in the expression of costimulatory molecules between the transfected DCs and non-transfected DCs. In MLR, the proliferation of T lymphocyte cells was inhibited by transfected DCs, but the control DCs stimulated the proliferation strongly. Conclusion DCs overexpressing Serratel could inhibit the proliferation and activation of T cells, which was not related to the expression of costimulatory molecules on DCs but via the Notchl-Serratel signaling pathway.
出处 《第三军医大学学报》 CAS CSCD 北大核心 2005年第17期1732-1734,共3页 Journal of Third Military Medical University
基金 国家自然科学基金资助项目(30300148)~~
关键词 Serratel 树突状细胞 免疫耐受 Serratel dendritic cells immune tolerance
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同被引文献26

  • 1夏俊波,吴奎,孙鲲,王长征.小鼠骨髓来源的树突状细胞体外扩增与鉴定[J].第三军医大学学报,2005,27(10):942-944. 被引量:13
  • 2冯剑锷,孙宗全,史嘉玮,高开柱.低剂量粒巨噬细胞集落刺激因子培养小鼠骨髓源性未成熟树突状细胞的实验研究[J].中华实验外科杂志,2006,23(2):221-223. 被引量:13
  • 3孙鲲,林科雄,吴奎,王长征.CD_4^+ CD_(25)^+T淋巴细胞对支气管哮喘小鼠气道炎症的影响及作用机制[J].中华结核和呼吸杂志,2006,29(2):109-112. 被引量:15
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  • 6McKenzie GJ, Khan M, Briend E, et al. Notch: a unique therapeutic target for immunomodulation. Expert Opin Ther Targets ,2005,9:395-410.
  • 7Dallman MJ, Champion B, Lamb JR. Notch signalling in the peripheral immune system. Novartis Found Symp, 2003,252 : 268- 278.
  • 8Hoyne GF, Le Roux I, Corsin-Jimenez M, et al. Serratel-induced notch signalling regulates the decision between immunity and tolerance made by peripheral CD4 ( + ) T ceils. Int Immunol, 2000,12 : 177-185.
  • 9Vamum-Finney B, Brashem-Stein C, Bernstein ID. Combined effects of Notch signaling and cytokines induce a multiple log increase in precursors with lymphoid and myeloid reconstituting ability. Blood ,2003,101 : 1784-1789.
  • 10Sakaguchi S, Wing K, Miyara M. Regulatory T cells-a brief history and perspective. Eur J Immunol,2007,37 Suppl 1 : S116-123.

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