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Norway

PMID:15041039  

Autoimmune diabetes is blocked in Stat4-deficient mice.

Zandong Yang | Meng Chen | Justin D Ellett | Lawrence B Fialkow | Jeffrey D Carter | Marcia McDuffie | Jerry L Nadler
Journal of autoimmunity | 2004

Signal transducers and activators of transcription (STAT) proteins are activated in response to many cytokines, growth factors and hormones. STAT4 mediates IL-12 signaling and regulates T helper 1 (Th1) cell differentiation. Both IL-12 and Th1 cell activation participate in the development of autoimmune diabetes. In this study, we investigated the role of STAT4 in autoimmune diabetes. We crossbred Stat4 deficient (Stat4-/-) mice with nonobese diabetic (NOD) mice to generate the Stat4-/- NOD model. In Stat4-/- NOD mice, serum levels of both IFN-gamma and IL-2 were significantly reduced as compared to the controls. Insulin secretion in pancreatic islets was preserved in Stat4-/- NOD mice. Significantly, disruption of Stat4 activation completely prevented the development of spontaneous diabetes in NOD mice. This study reveals the important role of STAT4 in autoimmune diabetes pathogenesis.

Pubmed ID: 15041039

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Associated grants

  • Agency: NIDDK NIH HHS, United States
    Id: DK062610
  • Agency: NIDDK NIH HHS, United States
    Id: DK063521
  • Agency: NIDDK NIH HHS, United States
    Id: DK063609
  • Agency: NICHD NIH HHS, United States
    Id: HD28934

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Jackson Laboratory (tool)

RRID:SCR_004633

An independent, nonprofit organization focused on mammalian genetics research to advance human health. Their mission is to discover the genetic basis for preventing, treating, and curing human disease, and to enable research for the global biomedical community. Jackson Laboratory breeds and manages colonies of mice as resources for other research institutions and laboratories, along with providing software and techniques. Jackson Lab also conducts genetic research and provides educational material for various educational levels.

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