4.6 Article

Evidence that Cd101 Is an Autoimmune Diabetes Gene in Nonobese Diabetic Mice

期刊

JOURNAL OF IMMUNOLOGY
卷 187, 期 1, 页码 325-336

出版社

AMER ASSOC IMMUNOLOGISTS
DOI: 10.4049/jimmunol.1003523

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资金

  1. National Institute of Allergy and Infectious Diseases (NIAID) [P01AI039671]
  2. Wellcome Trust [079895]
  3. Juvenile Diabetes Research Foundation (JDRF)
  4. National Institute for Health Research Biomedical Research Centre
  5. Lupus Research Institute
  6. University of Cincinnati microbial pathogenesis core center, Public Health Service [P30 DK078392]
  7. National Institute of Diabetes and Digestive and Kidney Diseases [R01DK084054]
  8. German Research Foundation Deutsche Forschungsgemeinschaft [MA 2621/2-1]
  9. Interdisciplinary Center for Clinical Research of the Universitatsklinikum Erlangen [IZKF_JB10_A48]
  10. Immune Tolerance Network [AI 15416]
  11. JDRF International
  12. Merck Genome Research Institute
  13. National Institute for Health Research [NF-SI-0508-10275] Funding Source: researchfish

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We have previously proposed that sequence variation of the CD101 gene between NOD and C57BL/6 mice accounts for the protection from type 1 diabetes (T1D) provided by the insulin-dependent diabetes susceptibility region 10 (Idd10), a <1 Mb region on mouse chromosome 3. In this study, we provide further support for the hypothesis that Cd101 is Idd10 using haplotype and expression analyses of novel Idd10 congenic strains coupled to the development of a CD101 knockout mouse. Susceptibility to T1D was correlated with genotype-dependent CD101 expression on multiple cell subsets, including Foxp3(+) regulatory CD4(+) T cells, CD11c(+) dendritic cells, and Gr1(+) myeloid cells. The correlation of CD101 expression on immune cells from four independent Idd10 haplotypes with the development of T1D supports the identity of Cd101 as Idd10. Because CD101 has been associated with regulatory T and Ag presentation cell functions, our results provide a further link between immune regulation and susceptibility to T1D. The Journal of Immunology, 2011, 187: 325-336.

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