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肾上腺髓质素在幽门螺杆菌感染中的表达调控及其功能的初步研究
引用本文:郭刚,吕一品,刘毓刚,滕永生,彭六生,毛方圆,庄园,孔辉.肾上腺髓质素在幽门螺杆菌感染中的表达调控及其功能的初步研究[J].第三军医大学学报,2018(3):183-189.
作者姓名:郭刚  吕一品  刘毓刚  滕永生  彭六生  毛方圆  庄园  孔辉
作者单位:陆军军医大学(第三军医大学)药学与检验医学系微生物与生化药学教研室,重庆,400038
基金项目:the General Program of National Natural Science Foundation of China ,国家自然科学基金面上项目
摘    要:目的 探讨肾上腺髓质素(adrenomedullin,ADM)在幽门螺杆菌感染中的表达调控及其对CD3+T细胞增殖的影响.方法 建立幽门螺杆菌(Helicobacter pylori,H.pylori)感染C57小鼠及胃上皮细胞模型,运用定量PCR、免疫组织化学染色和Western blot检测ADM的表达;并在细胞模型中探讨H.pylori感染诱导ADM上调的机制;利用ADM刺激CD3+T细胞,检测其对T细胞增殖的影响.结果 H.pylori感染可诱导胃上皮细胞AGS和HGC-27上调ADM的表达,并具有时间和感染菌量依赖性(P<0.05);PI3 K/AKT信号通路阻断可显著抑制H.pylori感染诱导的ADM上调表达(P<0.05);相对于未感染组,H.pylori感染小鼠胃组织中的ADM水平也显著增高;而相对于野生型全毒株,敲除cagA基因后,H.pylori感染诱导ADM上调的能力则显著下降(P <0.05);ADM能够以剂量依赖的方式诱导CD3+T细胞的增殖并促进IFN-y的表达(P<0.05).结论 幽门螺杆菌感染可经PI3K/AKT信号诱导肾上腺髓质素的表达上调,后者则可能通过影响CD3+T细胞的增殖和分化而发挥免疫调节作用.

关 键 词:幽门螺杆菌  肾上腺髓质素  PI3K/AKT信号通路  CD3+T细胞  Helicobacter  pylori  adrenomedullin  PI3K/AKT  signaling  pathway  CD3+  T  cells

Role and mechanism of adrenomedullin expression in Helicobacter pylori infection
GUO Gang,LYU Yipin,LIU Shugang,TENG Yongsheng,PENG Liusheng,MAO Fangyuan,ZHUANG Yuan,KONG Hui.Role and mechanism of adrenomedullin expression in Helicobacter pylori infection[J].Acta Academiae Medicinae Militaris Tertiae,2018(3):183-189.
Authors:GUO Gang  LYU Yipin  LIU Shugang  TENG Yongsheng  PENG Liusheng  MAO Fangyuan  ZHUANG Yuan  KONG Hui
Abstract:Objective To explore the expression regulation of adrenomedullin (ADM) in Helicobacter pylori (H.pylori) infection and its effect on the proliferation of CD3 + T cells.Methods H.pylori infection model was established in C57 mice and gastric epithelial cell lines (AGS and HGC-27).RT-PCR was used to detect the expression of ADM in the cells incubated with or without H.pylori.The protein levels of ADM,AKT and p-AKT were detected by Western blotting.The function of ADM on the proliferation of CD3 + T cells were evaluated by flow cytometry.Results H.pylori infection increased the expression of ADM in AGS cells and HGC-27 cells in a time-and dose-dependent manner (P < 0.05).While,blocking PI3K/AKT signal pathway reversed above increase induced by H.pylori (P < 0.05).Compared with uninfected mice,the infection also enhanced the ADM expression in the mouse gastric tissue.Compared with WT H.pylori infected AGS and HGC-27 cells,knockout of cagA resulted in decrease in ADM expression which was induced by H.pylori infection (P < 0.05).ADM induced the proliferation of CD3 + T cells in a dose-dependent manner,and enhanced the expression of IFN-γ (P < 0.05).Conclusion H.pylori infection up-regulates ADM expression through PI3K/AKT signaling pathway activation,and ADM exerts immunoregulatory effect by promoting proliferation and IFN-γproduction of CD3 + T cells.
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