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幽门螺杆菌 26695 株分泌蛋白 HP1286 诱导 AGS 细胞凋亡。

Secreted protein HP1286 of Helicobacter pylori strain 26695 induces apoptosis of AGS cells.

机构信息

National Institute for Communicable Disease Control and Prevention, Chinese Center for Disease Control and Prevention, Beijing 102206, China.

出版信息

Biomed Environ Sci. 2012 Dec;25(6):614-9. doi: 10.3967/0895-3988.2012.06.002.

Abstract

OBJECTIVE

Secreted proteins of Helicobacter pylori (H. pylori) interact with gastric epithelium cells and may contribute to cell damage. Considering the fact that HP0175 and hypothetical conserved protein HP1286 are included in the group and that HP0175 is a well-known apoptosis-induced factor, the present study aims to clarify whether HP1286 plays a role in bacterial pathogenicity or even functions as an apoptosis-induced factor in human stomach.

METHODS

Two genes encoding HP1286 and HP0175 were cloned into pET32a vector and expressed as recombinant proteins in Escherichia coli (E. coli) BL21. Signal peptide sequences were not included. The recombinant proteins were purified with His SpinTrap and desalted by using HiTrap Desalting. Immunoreactivity of the proteins was determined by Western blot. Human gastric epithelial cell AGS was challenged with these endotoxin-free proteins; and apoptosis of cells was assayed with the Cell Death ELISA kit.

RESULTS

Recombinant proteins and their respective products whose N-terminal his-tag were removed with thrombin were recognized by serum from the patient infected with H. pylori. Apoptotic AGS cells challenged by HP1286 of H. pylori 26695 were four times more than untreated cells. In addition, apoptosis-induced ability of HP1286 of SS1 was not as strong as that of H. pylori 26695 strain.

CONCLUSION

HP1286 of H. pylori 26695 induces apoptosis of AGS cells in a time-dependent manner, however the apoptosis-induced ability of HP1286 may differ due to variations between different strains.

摘要

目的

幽门螺杆菌(H. pylori)分泌的蛋白与胃上皮细胞相互作用,可能导致细胞损伤。鉴于 HP0175 和假定的保守蛋白 HP1286 均属于该组,并且 HP0175 是一种众所周知的凋亡诱导因子,本研究旨在阐明 HP1286 是否在细菌致病性中发挥作用,甚至在人胃中是否作为凋亡诱导因子发挥作用。

方法

克隆编码 HP1286 和 HP0175 的两个基因,并将其插入 pET32a 载体中,在大肠杆菌(E. coli)BL21 中表达为重组蛋白。不包括信号肽序列。使用 His SpinTrap 纯化重组蛋白,并使用 HiTrap Desalting 进行脱盐。通过 Western blot 测定蛋白质的免疫反应性。用这些无内毒素的蛋白刺激人胃上皮细胞 AGS;并用细胞死亡 ELISA 试剂盒测定细胞凋亡。

结果

用凝血酶去除 N 端 His 标签的重组蛋白及其各自的产物被感染 H. pylori 的患者血清识别。用 H. pylori 26695 的 HP1286 刺激的凋亡 AGS 细胞是未处理细胞的四倍。此外,SS1 菌株的 HP1286 的诱导凋亡能力不如 H. pylori 26695 菌株强。

结论

H. pylori 26695 的 HP1286 以时间依赖性方式诱导 AGS 细胞凋亡,但是由于不同菌株之间的差异,HP1286 的诱导凋亡能力可能不同。

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