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Proc Natl Acad Sci U S A ; 105(34): 12439-44, 2008 Aug 26.
Artigo em Inglês | MEDLINE | ID: mdl-18716002

RESUMO

With the goal of identifying changes in gene expression in CD4(+) T cells during the development of diabetes in the nonobese diabetic (NOD) mouse, we used DNA microarrays to analyze gene expression in CD4(+) T cells from the pancreatic draining lymph nodes of NOD/BDC 2.5 T cell receptor transgenic and WT NOD mice at different ages. At 4 and 6 weeks of age, we found up-regulation of a number of genes that are known to be induced by IFN-alpha. IFN-alpha levels and IFN-alpha-producing plasmacytoid dendritic cells were increased in the PLNs of 3- to 4-week-old NOD mice. Moreover, blockade of IFN-alpha receptor 1 in NOD mice by a neutralizing antibody at 2-3 weeks of age significantly delayed the onset and decreased the incidence of type 1 diabetes, increased the relative number of immature dendritic cells in the PLNs, and enhanced the ability of spleen CD4(+) T cells to produce IL-4 and IL-10. These findings demonstrate that IFN-alpha in the PLNs is an essential initiator in the pathogenesis of type 1 diabetes in NOD mice.


Assuntos
Diabetes Mellitus Tipo 1/etiologia , Interferon-alfa/fisiologia , Receptor de Interferon alfa e beta/fisiologia , Animais , Linfócitos T CD4-Positivos/metabolismo , Células Dendríticas/citologia , Diabetes Mellitus Tipo 1/patologia , Perfilação da Expressão Gênica , Interferon-alfa/análise , Interferon-alfa/farmacologia , Interleucina-10/biossíntese , Interleucina-4/biossíntese , Camundongos , Camundongos Endogâmicos NOD , Camundongos Transgênicos , Pâncreas/citologia , Pâncreas/imunologia , Regulação para Cima/efeitos dos fármacos
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