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作 者:张帆[1] 邵红伟[1] 沈晗[1] 张文峰[1] 吴凤麟[1] 黄树林[1]
机构地区:[1]广东药学院生命科学与生物制药学院,生物制药研究所,广东广州510006
出 处:《中国病理生理杂志》2009年第8期1505-1508,共4页Chinese Journal of Pathophysiology
基 金:国家自然科学基金资助项目(No.30572124);广东省自然科学基金资助项目(No.034046);广东省科技计划资助项目(No.2004B31201001)
摘 要:目的:研究肝癌特异性识别基因TCRVβ7.1表达重组体转染外周血单个核细胞(PBMCs)后对T细胞细胞因子表达的影响和信号通路的激活作用。方法:以肝癌特异性T细胞受体Vβ7.1转染PBMCs,流式细胞仪检测TCRVβ7.1表达量;Western blotting检测ERK1/2表达量及磷酸化水平(p-ERK)的改变;用ELISA法检测白细胞介素-4(IL-4)、γ-干扰素(IFN-γ)的表达量。结果:TCRVβ7.1基因转染健康人PBMCs并得到有效表达,转染TCRVβ7.1基因的PBMCs与肝癌细胞共培养后ERK蛋白磷酸化水平明显高于未转染组(P<0.01)。p-ERK1/2水平与T细胞激活有关。ELISA结果表明,转染PBMCs细胞与肝癌细胞共培养后,IFN-γ水平明显高于未转染组,而IL-4无明显改变。结论:TCRVβ7.1转染PBMCs与肝癌细胞共培养后,ERK信号通路被激活,IFN-γ表达增高。AIM : To investigate the effect of tumor - specific T cell receptor (TCR) gene transfection on production of cytokine and signaling activation in T cells. METHODS: TCRVβ7. 1 gene was transferred into peripheral blood mononuclear cells (PBMCs) obtained from healthy adults, and the expression of Vβ7. 1 was detected by flow cytometry before and after transfection. The total quantities of protein and phosphorylation of ERK1/2 were detected by Western blotting. The expressions of IL - 4 and IFN - γ were detected by ELISA. RESULTS : The results of flow cytometry showed that TCRVβ7. 1 protein was efficiently expressed after transfecfion. The phosphorylation level of ERK increased significantly in TCRVβ7. 1 - modified PBMCs, and was related with the activation of T cells. The expression of IFN - γ was significantly higher in TCR -transfected cells than that in non -transfected cells. The expression of IL -4, however, has no distinct difference between groups. CONCLUSION: The transfection of TCRVβ7. 1 induces phosphorylation of ERK1/2 and production of IFN - γ, and activates T lymphocytes.
关 键 词:基因 TCRVβ7.1 基因转染 细胞外信号调节激酶类 干扰素Γ
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