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纸质出版:2016
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王虎,杨俊霞,黄家君,周运江,随何欢,朱江,吴友莉,段光杰.髓样分化蛋白-2模拟肽抑制巨噬细胞吞噬革兰阴性菌[J].陆军军医大学学报(原第三军医大学学报),2016,38(08):805-810.
Wang Hu,Yang Junxia,Huang Jiajun,Zhou Yunjiang,Sui Hehuan,Zhu Jiang,Wu Youli,Duan Guangjie.Inhibitory effect of myeloid differentiation protein-2 mimetic peptide on phagocytosis of macrophage to Gram-negative bacteria[J].J Amry Med Univ (J Third Mil Med Univ),2016,38(08):805-810.
王虎,杨俊霞,黄家君,周运江,随何欢,朱江,吴友莉,段光杰.髓样分化蛋白-2模拟肽抑制巨噬细胞吞噬革兰阴性菌[J].陆军军医大学学报(原第三军医大学学报),2016,38(08):805-810. DOI:
Wang Hu,Yang Junxia,Huang Jiajun,Zhou Yunjiang,Sui Hehuan,Zhu Jiang,Wu Youli,Duan Guangjie.Inhibitory effect of myeloid differentiation protein-2 mimetic peptide on phagocytosis of macrophage to Gram-negative bacteria[J].J Amry Med Univ (J Third Mil Med Univ),2016,38(08):805-810. DOI:
目的 探讨髓样分化蛋白-2模拟肽(MD-2 mimetic peptide,MDMP)对巨噬细胞吞噬革兰阴性菌的影响及所致炎症因子分泌的抑制效应。 方法 采用PCR从pEGFP-C3质粒中扩增出表达EGFP的基因片段,通过基因重组构建原核表达载体pET-32a(+)-EGFP,经测序鉴定后,转化至大肠杆菌BL21(DE3)PLysS中筛选出稳定表达的重组菌pET-32a(+)-EGFP-BL21(DE3)PLysS(简称为EGFP-BL21)。以IPTG诱导重组质粒表达后,通过免疫荧光和流式细胞术检测RAW264.7细胞对EGFP-BL21的吞噬能力以验证EGFP-BL21的构建情况。进一步检测RAW264.7细胞对经不同浓度MDMP(1.0、10、100 μg/mL)预处理后的EGFP-BL21的吞噬效应;采用ELISA检测细胞培养上清液中TNF-α和IL-6的分泌水平。 结果 筛选获得稳定表达EGFP的重组大肠杆菌BL21(DE3)PLysS,重组菌经巨噬细胞RAW264.7吞噬后流式和激光共聚焦检测结果显示细胞内出现明显的绿色荧光。MDMP预处理后,流式检测结果显示RAW264.7细胞对EGFP-BL21的吞噬能力受到明显抑制,预处理组(10、100 μg/mL)的吞噬系数(PI)显著低于经血清调理的阳性对照组(P0.01),且细胞培养上清TNF-α和IL-6的分泌水平显著降低(P0.01)。 结论 MDMP预处理可明显抑制RAW264.7细胞对革兰阴性菌的吞噬作用,并降低该过程中炎症因子TNF-α和IL-6的分泌。
Objective To investigate the inhibitory effect of myeloid differentiation protein-2 mimetic peptide (MDMP) on the phagocytosis of macrophage to Gram-negative bacteria and on TNF-α and IL-6 secretion in this process. Methods Enhanced green fluorescent protein (EGFP) gene fragment was amplified from pEGFP-C3 plasmid by PCR. The prokaryotic expression vector pET-32a(+)-EGFP was constructed by gene recombination. After sequencing
Escherichia coli BL21 (DE3) PLysS was transformed with the vector to screen recombinant bacteria pET-32a(+)-EGFP-BL21 (DE3) PLysS (EGFP-BL21) with stable expression of EGFP. The expression of recombinant plasmid was induced with IPTG
and the phagocytic ability of RAW264.7 cells to EGFP-BL21 was detected by immunofluorescence assay and flow cytometry. And then
the effect of MDMP (1
10 and 100 μg/mL) on the phagocytosis of RAW264.7 cells to EGFP-BL21 was analyzed by flow cytometry
and the secretion of IL-6 and TNF-α was measured by ELISA. Results Recombinant Escherichia coli EGFP-BL21 with stable expression of EGFP was obtained. After pretreatment with MDMP
the phagocytosis of RAW264.7 cells to EGFP-BL21 was significantly inhibited
and the phagocytic index (PI) of the pretreatment group (10 and 100 μg/mL) was significantly lower than that of the positive control group (P0.01). Furthermore
MDMP (10 and 100 μg/mL) significantly decreased the secretion of TNF-α and IL-6 in EGFP-BL21-stimulated RAW264.7 cells. Conclusion MDMP pretreatment can inhibit the phagocytosis of RAW264.7 cells to Gram-negative bacteria
and reduce the secretion of inflammatory factors such as TNF-α and IL-6.
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