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作 者:孙晓琳[1] 谢基明[2] 云小乐[1] 张威[1] 康鸿斌[3] 万永青[1] 刘竟然[1] 巩培[1] 赵世敏[1] 王玉珍[1]
机构地区:[1]内蒙古农业大学生命科学学院,呼和浩特010018 [2]内蒙古自治区人民医院检验科,呼和浩特010018 [3]内蒙古医科大学第一附属医院,呼和浩特010018
出 处:《中国免疫学杂志》2015年第3期295-299,共5页Chinese Journal of Immunology
基 金:国家自然科学基金(81260662;31270922);内蒙古自然科学基金(2010MS0513;2011MS1112;2012 MS1156)
摘 要:目的:建立稳定表达Rab5a及其失活突变体Rab5a N133I巨噬细胞系,并分析Rab5a对LPS刺激的RAW264.7巨噬细胞中i NOS、TNF-α和IL-6表达的影响。方法:将Rab5a及其失活突变载体Rab5a N133I转染RAW264.7细胞,通过G418筛选稳定表达细胞系。通过Real-time PCR鉴定稳定表达细胞系。MTT法分析其生长特性,LPS刺激稳定表达细胞系不同时间,检测i NOS、TNF-α和IL-6的表达水平。结果:转染Rab5a/Rab5a N133I细胞Rab5a mRNA水平显著高于对照(P<0.05)。Rab5a过表达促进RAW264.7细胞增殖,而过表达Rab5a N133I细胞增殖显著慢于对照(P<0.05)。Rab5a过表达后,LPS诱导的RAW264.7细胞中i NOS、TNF-α和IL-6的表达显著增高(P<0.01)。然而,过表达Rab5a N133I对LPS诱导的i NOS、TNF-α和IL-6的表达没有显著影响。结论:Rab5a过表达显著促进了LPS活化的RAW264.7细胞中i NOS、TNF-α和IL-6的表达,这种促进作用依赖于其结合GTP的能力。Objective: To establish cell lines stably expressing RabSa and its the inactive mutant RabSaN133I, analyze the effect of Rab5a on the expression of cytokines in LPS-stimulated RAW264.7 cells . Methods:RAW264.7 cells were transfected with RabSa and its inactive mutant vector RabSa N133I separately, and then screened by G418. Rab5a stable expressing cell lines were identified by Real time-PCR. The growth of the stable cell lines was analyzed by MTT assay. After the stable cell lines were stimulated by LPS for different time periods, the expression of iNOS, TNF-α and IL-6 was detected. Results: RabSa and Rab5 aN1331 transfection resulted in elevated RabSa mRNA expression compared with the control cells ( P 〈 0. 05 ). RabSa overexpression enhanced the proliferation of RAW264.7 cells. However,the proliferation of RabSaN133I cells was significantly slower than the control cells (P〈 0. 05). Overexpression of RabSa promoted LPS-induced production of iNOS, TNF-α and IL-6 in RAW264. 7 cells (P〈0.01). Conversely,overexpression of Rab5aN133I abolished the stimulating effects of RabSa. Conclusion: RabSa promoted LPS-induced expression of iNOS,TNF-α and IL-6 in RAW264.7 macrophages in a GTP-bindina ability-dependent manner.
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