• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

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

小鼠结肠炎模型的组织形态学评分:评估结肠炎和结肠炎相关癌症的实用指南。

Histomorphological scoring of murine colitis models: A practical guide for the evaluation of colitis and colitis-associated cancer.

作者信息

Remke Marianne, Groll Tanja, Metzler Thomas, Urbauer Elisabeth, Kövilein Janine, Schnalzger Theresa, Ruland Jürgen, Haller Dirk, Steiger Katja

机构信息

Institute of Pathology, School of Medicine and Health, Technical University of Munich, Trogerstr. 18, 81675 Munich, Germany; Comparative Experimental Pathology, School of Medicine and Health, Technical University of Munich, Trogerstr. 18, 81675 Munich, Germany; Member of the German Cancer Consortium (DKTK), Partner Site Munich, Munich, Germany.

Institute of Pathology, School of Medicine and Health, Technical University of Munich, Trogerstr. 18, 81675 Munich, Germany; Comparative Experimental Pathology, School of Medicine and Health, Technical University of Munich, Trogerstr. 18, 81675 Munich, Germany.

出版信息

Exp Mol Pathol. 2024 Dec;140:104938. doi: 10.1016/j.yexmp.2024.104938. Epub 2024 Oct 16.

DOI:10.1016/j.yexmp.2024.104938
PMID:39418944
Abstract

BACKGROUND AND AIMS

Histomorphology is a powerful and cost-efficient tool for evaluating inflammatory and neoplastic conditions. Inflammatory bowel disease (IBD) is a widespread condition with globally rising incidences, and a lot of research is done to better understand the pathogenesis of IBD and to identify potential therapeutic approaches. However, standardized and reproducible scores for the histomorphological evaluation of murine IBD models are lacking. Therefore, we aimed to develop an easy-to-use and reproducible score for standardized assessment of colitis and associated cancer models.

METHODS

In this study, samples from three different colitis models with and without associated cancer formation were analyzed to develop a universal, robust, and reproducible score for the grading of murine colitis models using the following three parameters: 1. Extent of leucocyte infiltration, 2. Tissue damage, 3. Architectural disruption of the mucosa.

RESULTS

A scoring system was established for different kinds of colitis models (genetically induced enterocolitis, genetically induced metabolic injury, and chemically induced colitis-associated cancer) and all stages of the disease, from mild inflammatory changes to severe inflammation with neoplastic changes as the extreme extent of IBD. The scoring scheme is easy to use, can easily be learned, and proves to have a high interrater reliability.

CONCLUSIONS

We propose a robust histological scoring system for the assessment of murine colitis and colitis-associated cancer models, giving more researchers access to conclusive and reliable histological assessment.

摘要

背景与目的

组织形态学是评估炎症和肿瘤性疾病的一种强大且经济高效的工具。炎症性肠病(IBD)是一种广泛存在且全球发病率不断上升的疾病,人们开展了大量研究以更好地理解IBD的发病机制并确定潜在的治疗方法。然而,目前缺乏用于小鼠IBD模型组织形态学评估的标准化且可重复的评分系统。因此,我们旨在开发一种易于使用且可重复的评分系统,用于对结肠炎及相关癌症模型进行标准化评估。

方法

在本研究中,我们分析了来自三种不同的结肠炎模型(伴有或不伴有相关癌症形成)的样本,以使用以下三个参数开发一种通用、稳健且可重复的小鼠结肠炎模型分级评分系统:1. 白细胞浸润程度;2. 组织损伤;3. 黏膜结构破坏。

结果

针对不同类型的结肠炎模型(基因诱导的小肠结肠炎、基因诱导的代谢损伤以及化学诱导的结肠炎相关癌症)以及疾病的所有阶段,从轻度炎症变化到伴有肿瘤变化的严重炎症(作为IBD的极端情况),建立了一种评分系统。该评分方案易于使用,容易掌握,并且具有较高的评分者间可靠性。

结论

我们提出了一种用于评估小鼠结肠炎及结肠炎相关癌症模型的稳健的组织学评分系统,使更多研究人员能够进行结论性且可靠的组织学评估。

相似文献

1
Histomorphological scoring of murine colitis models: A practical guide for the evaluation of colitis and colitis-associated cancer.小鼠结肠炎模型的组织形态学评分:评估结肠炎和结肠炎相关癌症的实用指南。
Exp Mol Pathol. 2024 Dec;140:104938. doi: 10.1016/j.yexmp.2024.104938. Epub 2024 Oct 16.
2
GPR65 (TDAG8) inhibits intestinal inflammation and colitis-associated colorectal cancer development in experimental mouse models.GPR65(TDAG8)抑制实验性小鼠模型中的肠道炎症和结肠炎相关结直肠癌的发展。
Biochim Biophys Acta Mol Basis Dis. 2022 Jan 1;1868(1):166288. doi: 10.1016/j.bbadis.2021.166288. Epub 2021 Oct 8.
3
Investigating intestinal inflammation in DSS-induced model of IBD.在葡聚糖硫酸钠(DSS)诱导的炎症性肠病(IBD)模型中研究肠道炎症。
J Vis Exp. 2012 Feb 1(60):3678. doi: 10.3791/3678.
4
T-cell branched glycosylation as a mediator of colitis-associated colorectal cancer progression: a potential new risk biomarker in inflammatory bowel disease.T细胞分支糖基化作为结肠炎相关结直肠癌进展的介质:炎症性肠病中一种潜在的新风险生物标志物。
J Crohns Colitis. 2025 Apr 4;19(4). doi: 10.1093/ecco-jcc/jjaf043.
5
Stromal Cell Subsets Show Model-Dependent Changes in Experimental Colitis and Affect Epithelial Tissue Repair and Immune Cell Activation.基质细胞亚群在实验性结肠炎中表现出模型依赖性变化,并影响上皮组织修复和免疫细胞激活。
Inflamm Bowel Dis. 2025 Apr 10;31(4):1051-1066. doi: 10.1093/ibd/izae255.
6
Cux1 transcription factor is induced in inflammatory bowel disease and protects against experimental colitis.Cux1 转录因子在炎症性肠病中被诱导,并可预防实验性结肠炎。
Inflamm Bowel Dis. 2010 Oct;16(10):1739-50. doi: 10.1002/ibd.21274.
7
Mouse Models of Colitis-Associated Colon Cancer.结肠炎相关结肠癌的小鼠模型。
Methods Mol Biol. 2021;2224:133-146. doi: 10.1007/978-1-0716-1008-4_10.
8
Extensive Histopathological Characterization of Inflamed Bowel in the Dextran Sulfate Sodium Mouse Model with Emphasis on Clinically Relevant Biomarkers and Targets for Drug Development.采用葡聚糖硫酸钠诱导的小鼠结肠炎模型对炎症性肠病进行广泛的组织病理学特征分析,重点关注具有临床相关性的生物标志物和药物研发靶点。
Int J Mol Sci. 2021 Feb 18;22(4):2028. doi: 10.3390/ijms22042028.
9
Serum Amyloid A Promotes Inflammation-Associated Damage and Tumorigenesis in a Mouse Model of Colitis-Associated Cancer.血清淀粉样蛋白 A 促进结肠炎相关癌症小鼠模型中炎症相关损伤和肿瘤发生。
Cell Mol Gastroenterol Hepatol. 2021;12(4):1329-1341. doi: 10.1016/j.jcmgh.2021.06.016. Epub 2021 Jul 2.
10
Reactivation of inflammatory bowel disease in a mouse model of depression.抑郁症小鼠模型中炎症性肠病的复发
Gastroenterology. 2009 Jun;136(7):2280-2288.e1-4. doi: 10.1053/j.gastro.2009.02.069. Epub 2009 Mar 9.

引用本文的文献

1
Susceptibility to inflammatory bowel diseases promotes invasive carcinomas in a murine model of ATF6-driven colon cancer.在ATF6驱动的结肠癌小鼠模型中,炎症性肠病易感性会促进侵袭性癌的发生。
J Crohns Colitis. 2025 Jul 3;19(7). doi: 10.1093/ecco-jcc/jjaf102.
2
Therapeutic potential of NRF2 activating drug RTA-408 in suppressing T cell effector responses and inflammatory bowel disease.NRF2激活药物RTA-408在抑制T细胞效应反应和炎症性肠病方面的治疗潜力。
J Immunol. 2025 Aug 1;214(8):1951-1968. doi: 10.1093/jimmun/vkaf117.
3
Anti-inflammatory effects and gut microbiota modulation of synbiotic mulberry in DSS-induced colitis rats.
合生元桑椹对葡聚糖硫酸钠诱导的结肠炎大鼠的抗炎作用及肠道微生物群调节作用
Mol Cell Biochem. 2025 May 21. doi: 10.1007/s11010-025-05309-9.
4
Multi-site investigation of gut microbiota in CDKL5 deficiency disorder mouse models: Targeting dysbiosis to improve neurological outcomes.CDKL5缺陷障碍小鼠模型中肠道微生物群的多中心研究:针对生态失调改善神经学结局。
Cell Rep. 2025 Apr 22;44(4):115546. doi: 10.1016/j.celrep.2025.115546. Epub 2025 Apr 10.
5
Clonal memory of colitis accumulates and promotes tumor growth.结肠炎的克隆记忆会累积并促进肿瘤生长。
Res Sq. 2025 Mar 27:rs.3.rs-6081101. doi: 10.21203/rs.3.rs-6081101/v1.
6
Epithelial genetic muscarinic receptor 3 ablation induces sex-specific modulation of colonic intestinal progenitor cells and response to intestinal injury.上皮基因毒蕈碱受体3缺失诱导结肠肠道祖细胞的性别特异性调节及对肠道损伤的反应。
J Crohns Colitis. 2025 Jun 4;19(6). doi: 10.1093/ecco-jcc/jjaf038.
7
Dietary protein source mediates colitis pathogenesis through bacterial modulation of bile acids.膳食蛋白质来源通过细菌对胆汁酸的调节介导结肠炎发病机制。
bioRxiv. 2025 Jan 27:2025.01.24.634824. doi: 10.1101/2025.01.24.634824.