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超抗原葡萄球菌肠毒素A拮抗伊马替尼抑制T细胞活化作用的研究

Superantigen SEA antagonizes inhibitory effect of imatinib on T cell activation

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【作者】 颜宇辉陈小华王冠明林晨李扬秋

【Author】 YAN Yu-hui;CHEN Xiao-hua;WANG Guan-ming;LIN Chen;LI Yang-qiu;Department of Microbiology and Immunology,School of Medicine,Jinan University;Institute of Hematology,Jinan University;

【机构】 暨南大学医学院微生物与免疫学系暨南大学血液研究所

【摘要】 目的:探讨葡萄球菌肠毒素A(staphylococcal enterotoxin A,SEA)对甲磺酸伊马替尼(imatinib mesylate,IM)抑制T淋巴细胞活化的影响。方法:2 mg/L SEA和50 nmol/L IM联合作用于Jurkat细胞24 h后,用实时荧光定量PCR技术检测CD3ε和ζ链mRNA表达水平变化;Western blotting技术检测CD3ε和ζ链蛋白水平变化。结果:单纯IM组CD3ε和ζ链mRNA及蛋白表达均表现下调;SEA与IM联合用药组可以逆转IM下调CD3ε和ζ链mRNA及蛋白表达水平作用。SEA拮抗IM抑制作用中,对CD3ε链mRNA表达上调的作用明显大于CD3ζ链。结论:SEA能拮抗IM对T细胞CD3ε和ζ链表达的抑制作用。

【Abstract】 AIM: To investigate the effects of staphylococcal enterotoxin A( SEA) on the inhibition of T lymphocyte activation induced by imatinib mesylate( IM). METHODS: Jurkat cells were stimulated with SEA( 2 mg / L) and IM( 5 nmol / L) for 24 h. The mRNA expression of CD3ε and ζ chains was measured by real-time fluorescence quantitative PCR. The protein levels of CD3ε and ζ chains were detected by Western blotting. RESULTS: The expression of CD3ε and ζ chains at mRNA and protein levels was down-regulated in the Jurkat cells stimulated by IM alone. These down-regulations of CD3ε and ζ chains were reversed by the stimulation of IM combined with SEA. The antagonistic effect of SEA on IM-mediated inhibition of CD3ε mRNA expression was significantly greater than that on CD3ζ mRNA. CONCLUSION: SEA antagonizes imatinib-mediated inhibitory effect on T cell activation.

【基金】 国家自然科学基金资助项目(No.81270604);广东省自然科学基金重点项目(No.S2013020012863);中央高校基本科研业务费专项资金资助项目(No.21612116)
  • 【文献出处】 中国病理生理杂志 ,Chinese Journal of Pathophysiology , 编辑部邮箱 ,2014年03期
  • 【分类号】R733.72
  • 【被引频次】1
  • 【下载频次】87
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