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雄性依赖性促进 129 小鼠感染 和 后的结肠炎

Male-Dependent Promotion of Colitis in 129 Mice Co-Infected with and .

机构信息

Division of Comparative Medicine, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.

出版信息

Int J Mol Sci. 2020 Nov 24;21(23):8886. doi: 10.3390/ijms21238886.

DOI:10.3390/ijms21238886
PMID:33255175
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7727654/
Abstract

The prevalence of gastric (Hp) infection is ~50% of the world population. However, how Hp infection influences inflammatory bowel disease in humans is not fully defined. In this study, we examined whether co-infection with Hp influenced (Hh)-induced intestinal pathology in mice. mice of both sexes were infected with Hh, of which a subgroup was followed by infection with Hp two weeks later. Co-infected males, but not females, had significantly higher total colitis index scores in the colon at both 10 and 21 weeks post-Hh infection (WPI) and developed more severe dysplasia at 21 WPI compared with mono-Hh males. There were no significant differences in colonization levels of gastric Hp and colonic Hh between sexes or time-points. In addition, mRNA levels of colonic , , , , , , and , which play important roles in the development and function of proinflammatory innate lymphoid cell groups 1 and 3, were significantly up-regulated in the dually infected males compared with mono-Hh males at 21 WPI. These data suggest that concomitant Hp infection enhances the inflammatory responses in the colon of-Hh-infected males, which results in more severe colitis and dysplasia.

摘要

全球约有 50%的人口感染幽门螺杆菌(Hp)。然而,Hp 感染如何影响人类炎症性肠病尚不完全清楚。在这项研究中,我们研究了 Hp 合并感染是否会影响 Hh 诱导的小鼠肠道病理。雌雄小鼠均感染 Hh,其中一部分在两周后感染 Hp。与单感染 Hh 的雄性小鼠相比,合并感染的雄性小鼠在感染 Hh 后 10 和 21 周(WPI)的结肠总结肠炎指数评分显著更高,并在 21 WPI 时发生更严重的异型增生,但雌雄小鼠的胃 Hp 和结肠 Hh 的定植水平在各时间点均无显著差异。此外,与单感染 Hh 的雄性小鼠相比,合并感染的雄性小鼠在 21 WPI 时结肠中与固有淋巴样细胞群 1 和 3 发育和功能相关的、 、 、 、 、 和 的 mRNA 水平显著上调。这些数据表明,Hp 合并感染增强了-Hh 感染雄性小鼠结肠的炎症反应,导致更严重的结肠炎和异型增生。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3efa/7727654/739e12d040ff/ijms-21-08886-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3efa/7727654/6524caefff33/ijms-21-08886-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3efa/7727654/bf73a180ae85/ijms-21-08886-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3efa/7727654/87aef559d3ef/ijms-21-08886-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3efa/7727654/16ff88fd5138/ijms-21-08886-g004a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3efa/7727654/739e12d040ff/ijms-21-08886-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3efa/7727654/6524caefff33/ijms-21-08886-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3efa/7727654/bf73a180ae85/ijms-21-08886-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3efa/7727654/87aef559d3ef/ijms-21-08886-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3efa/7727654/16ff88fd5138/ijms-21-08886-g004a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3efa/7727654/739e12d040ff/ijms-21-08886-g005.jpg

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