Defining the Transcriptional and Cellular Landscape of Type 1 Diabetes in the NOD Mouse

被引:95
作者
Carrero, Javier A. [1 ]
Calderon, Boris [1 ]
Towfic, Fadi [2 ]
Artyomov, Maxim N. [1 ]
Unanue, Emil R. [1 ]
机构
[1] Washington Univ, Sch Med, Dept Pathol & Immunol, St Louis, MO 63130 USA
[2] Immuneering Corp, Cambridge, MA USA
基金
美国国家卫生研究院;
关键词
DIABETOGENIC T-CELLS; INTERFERON-ALPHA; GENE-EXPRESSION; DENDRITIC CELLS; IFN-GAMMA; INDUCTION; ISLETS; AMPLIFICATION; PROGRESSION; LANGERHANS;
D O I
10.1371/journal.pone.0059701
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
Our ability to successfully intervene in disease processes is dependent on definitive diagnosis. In the case of autoimmune disease, this is particularly challenging because progression of disease is lengthy and multifactorial. Here we show the first chronological compendium of transcriptional and cellular signatures of diabetes in the non-obese diabetic mouse. Our data relates the immunological environment of the islets of Langerhans with the transcriptional profile at discrete times. Based on these data, we have parsed diabetes into several discrete phases. First, there is a type I interferon signature that precedes T cell activation. Second, there is synchronous infiltration of all immunological cellular subsets and a period of control. Finally, there is the killing phase of the diabetogenic process that is correlated with an NF-kB signature. Our data provides a framework for future examination of autoimmune diabetes and its disease progression markers.
引用
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页数:14
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