乳糜泻小鼠模型。

A Mouse Model of Celiac Disease.

机构信息

Department of Medicine, University of Chicago, Chicago, Illinois.

Celiac Disease Center, University of Chicago, Chicago, Illinois.

出版信息

Curr Protoc. 2022 Aug;2(8):e515. doi: 10.1002/cpz1.515.

Abstract

The design and use of mouse models that reproduce key features of human diseases are critical to advance our understanding of the pathogenesis of autoimmune diseases and to test new therapeutic strategies. Celiac disease is a unique organ-specific autoimmune-like disorder occurring in genetically susceptible individuals carrying HLA-DQ2 or HLA-DQ8 molecules who consume gluten. The key histological characteristic of the disease in humans is the destruction of the lining of the small intestine, a feature that has been difficult to reproduce in immunocompetent animal models. This unit describes the DQ8-D -villin-IL-15 transgenic mouse model of CeD, which was engineered based on the knowledge acquired from studying CeD patients' intestinal samples, and which represents the first animal model that develops villous atrophy in an HLA- and gluten-dependent manner without administration of any adjuvant. We provide detailed protocols for inducing and monitoring intestinal tissue damage, evaluating the cytotoxic properties of intraepithelial lymphocytes that mediate enterocyte lysis, and assessing the activation of the enzyme transglutaminase 2, which contributes to the generation of highly immunogenic gluten peptides. Detailed protocols to prepare pepsin-trypsin digested gliadin (PT-gliadin) or chymotrypsin-digested gliadin (CT-gliadin), which allow antibody detection against native or deamidated gluten peptides, are also provided in this unit. © 2022 The Authors. Current Protocols published by Wiley Periodicals LLC. Basic Protocol 1: Induction of celiac-like disease in DQ8-D -villin-IL-15tg mice Basic Protocol 2: Histological assessment of villous atrophy Support Protocol 1: Morphometric assessment of villous/crypt ratio Support Protocol 2: Evaluation of epithelial cells renewal Support Protocol 3: Evaluation of the density of intraepithelial lymphocytes Basic Protocol 3: Analysis of cytotoxic intraepithelial lymphocytes Basic Protocol 4: Transglutaminase 2 activation and measurement of antibodies against native and deamidated gluten peptides Support Protocol 4: Preparation of CT-gliadin Support Protocol 5: Preparation of PT-gliadin.

摘要

设计和使用能够重现人类疾病关键特征的小鼠模型对于深入了解自身免疫性疾病的发病机制以及测试新的治疗策略至关重要。乳糜泻是一种独特的器官特异性自身免疫样疾病,发生在携带 HLA-DQ2 或 HLA-DQ8 分子且摄入麸质的遗传易感个体中。人类疾病的关键组织学特征是小肠内层的破坏,这一特征在免疫活性动物模型中很难重现。本单元描述了基于从研究乳糜泻患者肠道样本中获得的知识设计的 DQ8-D -villin-IL-15 转基因乳糜泻小鼠模型,该模型是第一个以 HLA 和麸质依赖的方式发展绒毛萎缩而无需任何佐剂的动物模型。我们提供了诱导和监测肠道组织损伤、评估介导肠细胞溶解的上皮内淋巴细胞细胞毒性特性以及评估有助于产生高度免疫原性麸质肽的转谷氨酰胺酶 2 激活的详细方案。本单元还提供了制备胃蛋白酶-胰蛋白酶消化的麦胶(PT-麦胶)或糜蛋白酶消化的麦胶(CT-麦胶)的详细方案,这些方案允许针对天然或脱酰胺麸质肽检测抗体。 © 2022 作者。 Wiley Periodicals LLC 出版的《当代协议》。 基本方案 1:在 DQ8-D -villin-IL-15tg 小鼠中诱导乳糜泻样疾病 基本方案 2:绒毛萎缩的组织学评估 支持方案 1:绒毛/隐窝比的形态计量评估 支持方案 2:上皮细胞更新的评估 支持方案 3:上皮内淋巴细胞密度的评估 基本方案 3:分析细胞毒性上皮内淋巴细胞 基本方案 4:转谷氨酰胺酶 2 激活和针对天然和脱酰胺麸质肽的抗体分析 支持方案 4:CT-麦胶的制备 支持方案 5:PT-麦胶的制备。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dc5d/12016466/4fd7c5c251fb/CPZ1-2-0-g002.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索