The bm12 Inducible Model of Systemic Lupus Erythematosus (SLE) in C57BL/6 Mice

被引:38
作者
Klarquist, Jared [1 ,2 ]
Janssen, Edith M. [1 ,2 ]
机构
[1] Cincinnati Childrens Hosp Med Ctr, Div Immunobiol, Cincinnati, OH 45229 USA
[2] Univ Cincinnati, Coll Med, Cincinnati, OH 45221 USA
来源
JOVE-JOURNAL OF VISUALIZED EXPERIMENTS | 2015年 / 105期
关键词
Medicine; Issue; 105; T follicular helper cell (Tfh); germinal center (GC) B cell; plasma cell; ascites; flow cytometry; animal model; antinuclear antibody (ANA); autoimmunity; nephritis; trogocytosis; chronic graft-versus-host disease (cGVHD); type I interferon (IFN); CELLS; PREVALENCE;
D O I
10.3791/53319
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
Systemic lupus erythematosus (SLE) is an autoimmune disease with diverse clinical and immunological manifestations. Several spontaneous and inducible animal models mirror common components of human disease, including the bm12 transfer model. Upon transfer of bm12 splenocytes or purified CD4 T cells, C57BL/6 mice rapidly develop large frequencies of T follicular helper cells (Tfh), germinal center (GC) B cells, and plasma cells followed by high levels of circulating anti-nuclear antibodies. Since this model utilizes mice on a pure C57BL/6 background, researchers can quickly and easily study disease progression in transgenic or knockout mouse strains in a relatively short period of time. Here we describe protocols for the induction of the model and the quantitation Tfh, GC B cells, and plasma cells by multi-color flow cytometry. Importantly, these protocols can also be used to characterize disease in most mouse models of SLE and identify Tfh, GC B cells, and plasma cells in other disease models.
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页数:11
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