金黄色葡萄球菌α-溶血素突变体H35A抑制α-溶血素的细胞毒性
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全军“十三五”医学科技重点项目(BWS14J046);全军青年培育项目(14QNP041)


Staphylococcus aureus α-hemolysin mutant H35A inhibit cytotoxicity of wild α-hemolysin
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    摘要:

    目的:研究金黄色葡萄球菌α-溶血素(α-hemolysin,Hla)突变体H35A在人外周血单个核细胞(human peripheral blood mononuclear cells,hPBMC)和THP-1巨噬细胞中对于野生型Hla毒性作用的影响。方法:H35A与Hla共同作用于hPBMC和THP-1巨噬细胞,实时荧光定量PCR检测细胞中白介素(interleukin,IL)-1β、IL-6、肿瘤坏死因子(tumor necrosis factor,TNF)-α等炎症因子的mRNA转录水平差异,台盼蓝染色计算THP-1巨噬细胞存活率。结果:预孵育突变体H35A 1 h的hPBMC和THP-1巨噬细胞,经Hla刺激产生IL-1、IL-6、TNF-α的mRNA转录水平显著降低;台盼蓝染色计数发现,H35A与Hla共同作用的THP-1巨噬细胞存活率显著高于Hla单独处理组。结论:突变体H35A可抑制野生型Hla对于hPBMC和巨噬细胞的毒性作用,为金黄色葡萄球菌早期感染防治药物的研发提供了更多选择。

    Abstract:

    Objective:To study the effect of Staphylococcus aureus α-hemolysin mutant H35A on the wild type α-hemolysin(Hla) toxicity in human periphery blood mononuclear cells(hPBMC) and THP-1 macrophages. Methods: hPBMC and THP-1 macrophages were stimulated with both H35A and Hla. The transcriptions of interleukin-1β (IL-1β),interleukin-6 (IL-6),tumor necrosis factor-α(TNF-α) mRNA in hPBMC and THP-1 macrophages were assayed by real-time Q-PCR. The survival percentage of THP-1 macrophages treated with Hla and H35A was calculated with Trypan blue staining. Results: The transcriptions of IL-1,IL-6 and TNF-α mRNA in hPBMC and THP-1 macrophages treated with H35A mutant were significantly decreased upon stimulation with Hla. The survival percentage of THP-1 macrophages treated with Hla and H35A was significantly increased. Conclusion: H35A mutant can inhibit the toxic effect of Hla on human monocytes and macrophages,and it is expected to be a therapeutic drug used in the early stage of Staphylococcus aureus infection.

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孙倩男,郑 峰,周婷婷,岳 岩,王怡雯,朱旭辉,王长军,余伯阳,朱 进.金黄色葡萄球菌α-溶血素突变体H35A抑制α-溶血素的细胞毒性[J].南京医科大学学报(自然科学版),2017,(3):293-297

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  • 收稿日期:2016-09-01
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  • 在线发布日期: 2017-04-07
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