Induction of Murine Intestinal Inflammation by Adoptive Transfer of Effector CD4+CD45RBhigh T Cells into Immunodeficient Mice

被引:14
|
作者
Steinbach, Erin C. [1 ,2 ]
Gipson, Gregory R. [1 ]
Sheikh, Shehzad Z. [1 ,3 ,4 ]
机构
[1] Univ N Carolina, Ctr Gastrointestinal Biol & Dis, Chapel Hill, NC 27515 USA
[2] Univ N Carolina, Dept Microbiol & Immunol, Chapel Hill, NC 27515 USA
[3] Univ N Carolina, Dept Genet, Chapel Hill, NC 27515 USA
[4] Univ N Carolina, Curriculum Genet & Mol Biol, Chapel Hill, NC 27515 USA
来源
关键词
Immunology; Issue; 98; IBD; Colitis; Experimental Models; Adaptive Immunity; T cells; Mucosal Immunity; Inflammation; BOWEL-DISEASE; MICROBIOTA; COLITIS;
D O I
10.3791/52533
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
There are many different animal models available for studying the pathogenesis of human inflammatory bowel diseases (IBD), each with its own advantages and disadvantages. We describe here an experimental colitis model that is initiated by adoptive transfer of syngeneic splenic CD4(+)CD45RB(high) T cells into T and B cell deficient recipient mice. The CD4(+)CD45RB(high) T cell population that largely consists of naive effector cells is capable of inducing chronic intestinal inflammation, closely resembling key aspects of human IBD. This method can be manipulated to study aspects of disease onset and progression. Additionally it can be used to study the function of innate, adaptive, and regulatory immune cell populations, and the role of environmental exposures, i.e., the microbiota, in intestinal inflammation. In this article we illustrate the methodology for inducing colitis with a step-by-step protocol. This includes a video demonstration of key technical aspects required to successfully develop this murine model of experimental colitis for research purposes.
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页数:7
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