Kilham rat virus-induced type 1 diabetes involves beta cell infection and intra-islet JAK-STAT activation prior to insulitis

被引:13
作者
Alkanani, Aimon K. [1 ]
Hara, Naoko [1 ]
Gianani, Roberto [1 ]
Zipris, Danny [1 ]
机构
[1] Univ Colorado, Barbara Davis Ctr Childhood Diabet, Aurora, CO 80045 USA
关键词
Innate immunity; Islets; Janus kinase; Kilham rat virus; LEW1.WR1; rat; Signal transducer and activator of transcription; Type; 1; diabetes; TOLL-LIKE RECEPTOR-3; DOUBLE-STRANDED-RNA; PANCREATIC-ISLETS; BB/WOR RATS; BBDR RATS; PATHWAYS; EXPRESSION; PERTURBATION; INFLAMMATION; MECHANISMS;
D O I
10.1016/j.virol.2014.07.041
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
We used the LEW1.WR1 rat model of Kilham Rat Virus (KRV)-induced type 1 diabetes (T1D) to test the hypothesis that disease mechanisms are linked with beta cell infection and intra-islet immune activation prior to insulitis. KRV induces genes involved in type I and type II interferon pathways in islet cell lines in vitro and in islets from day-5-infected animals in vivo via mechanisms that do not involve insulitis, beta cell apoptosis, or impaired insulin expression. Immunohistochemistry studies indicated that KRV protein is expressed in beta cells 5 days following infection. KRV induces the phosphorylation of Janus Kinase 1/2 (JAK1/2) and signal transducer and activator of transcription 1 (STAT-1) in islet cells via a mechanism that could involve TLR9 and NF-kappa B pathways. These data demonstrate for the first time that KRV-induced islet destruction is associated with beta cell infection and intra-islet innate immune upregulation early in the disease process. (C) 2014 Elsevier Inc. All rights reserved.
引用
收藏
页码:19 / 27
页数:9
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