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首页> 外文期刊>American Journal of Pathology >Accelerated Progression of Gastritis to Dysplasia in the Pyloric Antrum of TFF2–/– C57BL6 x Sv129 Helicobacter pylori-Infected Mice
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Accelerated Progression of Gastritis to Dysplasia in the Pyloric Antrum of TFF2–/– C57BL6 x Sv129 Helicobacter pylori-Infected Mice

机译:TFF2-/ – C57BL6 x Sv129幽门螺杆菌感染的小鼠幽门窦胃炎加速发展为异型增生

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摘要

Trefoil factor family 2 (TFF2) is up-regulated in Helicobacter spp.-infected gastric tissues of both humans and mice. To ascertain the biological effects of TFF2 in vivo, TFF2–/– C57BL/6 x Sv129 and wild-type (WT) C57BL/6 x Sv129 mice were orally infected with Helicobacter pylori SS1. Mice were evaluated for gastric H. pylori colonization, pathology, and cytokine profiles at 6 and 19 months post inoculation (pi). At 6 months pi, there was a significant difference (P < 0.05) for epithelial criteria (mucosal defects, atrophy, hyperplasia, pseudopyloric metaplasia, and dysplasia) in the corpus of TFF2–/– versus WT mice. At 19 months pi, a similar statistical difference in epithelial parameters was noted in the antrum of TFF2–/– versus WT mice (P < 0.01). All of the TFF2–/– H. pylori-infected mice had high-grade antral dysplasia, including gastric intraepithelial neoplasia, which was statistically significant (P < 0.05) compared with the infected WT mice. Levels of interferon- were markedly elevated in the gastric mucosa of infected TFF2–/– mice at both 6 and 19 months pi. TFF2 provided a cytoprotective and/or anti-inflammatory effect against the progression of premalignant lesions of the gastric corpus at 6 months pi and in the pyloric antrum in H. pylori-infected mice at 19 months pi. These data support a protective role for TFF2 in part by modulating levels of gastric interferon- in the development of H. pylori-associated premalignancy of the distal stomach.
机译:三叶因子家族2(TFF2)在人和小鼠的幽门螺杆菌感染的胃组织中均上调。为了确定TFF2在体内的生物学作用,将TFF2-/ – C57BL / 6 x Sv129和野生型(WT)C57BL / 6 x Sv129小鼠口服幽门螺杆菌SS1。在接种后6和19个月(pi)评估小鼠的胃幽门螺杆菌定植,病理学和细胞因子谱。在pi的6个月时,与WT小鼠相比,TFF2-/-小鼠的上皮标准(粘膜缺损,萎缩,增生,假幽门化生和发育异常)有显着差异(P <0.05)。在pi的19个月时,与WT小鼠相比,TFF2-/-的胃窦上皮参数有相似的统计学差异(P <0.01)。所有TFF2-/-H.幽门螺杆菌感染的小鼠均具有高度的胃窦发育异常,包括胃上皮内瘤变,与感染的WT小鼠相比,具有统计学意义(P <0.05)。在感染后6个月和19个月,受感染的TFF2-/-小鼠的胃粘膜中干扰素水平显着升高。 TFF2在感染后6个月时对幽门螺杆菌感染小鼠的胃体癌前病变和幽门窦内的胃体癌变前病变的进展提供了细胞保护和/或抗炎作用。这些数据部分通过调节胃内干扰素水平来支持TFF2的保护作用,该水平在幽门螺杆菌相关的远端胃恶性肿瘤的发展中发挥了作用。

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