Suppr超能文献

鸟分枝杆菌副结核亚种亲脂抗原可导致小鼠患克罗恩病样坏死性结肠炎。

Mycobacterium avium subsp. paratuberculosis lipophilic antigen causes Crohn's disease-type necrotizing colitis in Mice.

作者信息

Momotani Eiichi, Ozaki Hiroshi, Hori Masatoshi, Yamamoto Shizuo, Kuribayashi Takashi, Eda Shigetoshi, Ikegami Masahiro

机构信息

Research Area of Pathology and Pathophysiology, National Institute of Animal Health, 3-1-5 Kan-nondai, Tsukuba, 305-0856 Japan.

出版信息

Springerplus. 2012 Dec;1(1):47. doi: 10.1186/2193-1801-1-47. Epub 2012 Nov 8.

Abstract

BACKGROUND

A 2,4,6-trinitrobenzene sulfonic acid (TNBS)-induced murine colitis model was developed to investigate the pathogenesis and to evaluate a method of treating human Crohn's disease. This experimental model rapidly induces colitis similar to human Crohn's disease lesion in a reproducible manner. However, natural exposure of the human digestive tract to TNBS is unrealistic. A novel animal model based on realistic data is eagerly anticipated in future research on pathogenesis of CD.

METHOD

We evaluated the potency of Map antigen molecules in an effort to develop a novel colitis model using a more realistic source than TNBS. We prepared the Map antigen by ethanol extraction and developed a mouse model in a manner similar to that of the well-known TNBS-induced colitis in mice. In the experiment, seven days after subcutaneous (SC) injection of the antigen into normal C57BL/6 mice, the same antigen in 50% ethanol was injected into the colon by the transanal route with a fine cannula.

RESULTS

On the fifth day after the transanal injection, histopathological examination revealed full-thickness necrotizing colitis with erosion and ulcers; severe infiltration with neutrophils, lymphocytes, macrophages, and perforation. However, no change was detected with each single Map-antigen injection.

CONCLUSION

The present results provide a novel animal model for research on CD and may be the key to clarifying the relationship between CD and Map. This is the first evidence that mycobacterium antigen induces necrotizing colitis.

摘要

背景

开发了一种2,4,6-三硝基苯磺酸(TNBS)诱导的小鼠结肠炎模型,用于研究发病机制并评估治疗人类克罗恩病的方法。该实验模型能以可重复的方式快速诱导出类似于人类克罗恩病病变的结肠炎。然而,人类消化道自然接触TNBS是不现实的。在未来关于克罗恩病发病机制的研究中,迫切期待基于实际数据的新型动物模型。

方法

我们评估了Map抗原分子的效力,试图使用比TNBS更符合实际情况的来源开发一种新型结肠炎模型。我们通过乙醇提取制备了Map抗原,并以类似于著名的TNBS诱导小鼠结肠炎的方式建立了小鼠模型。在实验中,将抗原皮下注射到正常C57BL/6小鼠体内7天后,用细插管经肛门途径将50%乙醇中的相同抗原注入结肠。

结果

经肛门注射后第5天,组织病理学检查显示全层坏死性结肠炎伴糜烂和溃疡;有大量中性粒细胞、淋巴细胞、巨噬细胞浸润及穿孔。然而,每次单独注射Map抗原均未检测到变化。

结论

目前的结果为克罗恩病研究提供了一种新型动物模型,可能是阐明克罗恩病与Map之间关系的关键。这是分枝杆菌抗原诱导坏死性结肠炎的首个证据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5591/3600126/5278127d7beb/40064_2012_128_Fig1_HTML.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验