Change search
ReferencesLink to record
Permanent link

Direct link
Preferential maturation of NOD T cells in the competitive environment of NODB6 embryo aggregation chimeric system
Umeå University, Faculty of Medicine, Department of Medical Biosciences.
(English)Manuscript (preprint) (Other academic)
National Category
Immunology in the medical area
URN: urn:nbn:se:umu:diva-4994OAI: diva2:144330
Available from: 2006-03-14 Created: 2006-03-14 Last updated: 2012-06-29Bibliographically approved
In thesis
1. The genetic basis of T and B cell contribution to autoimmune diabetes in NOD mice
Open this publication in new window or tab >>The genetic basis of T and B cell contribution to autoimmune diabetes in NOD mice
2006 (English)Doctoral thesis, comprehensive summary (Other academic)
Abstract [en]

The nonobese diabetic mouse (NOD) is an excellent animal model to study type 1 diabetes. As with some humans, disease in the NOD mouse is effected by a combination of genetic and environmental factors. At least 20 insulin dependent diabetes (Idd) susceptibility loci have been identified so far, both in humans and in the NOD mouse.

In this thesis, the overall aim has been to understand the genetic basis of diabetes in the NOD mouse by assessing immunogically-related phenotypes. As lymphocytes are the main players in the onset and progression to overt diabetes, we searched for physiological abnormalities in T and B cells, which could contribute to the breakdown of tolerance to pancreatic antigens. Ultimately, we postulate that abnormalities in the T or B cell compartments, under the genetic control of a previously defined diabetes susceptibility regions (Idds) could unravel the biological mechanisms underlying diabetes susceptibility and facilitate the identification of etiological polymorphisms involved in the disease.

NOD T cells are defective in upregulating CTLA-4 upon in vitro activation. Previous studies have shown that this defect is, at least in part, controlled by gene(s) in the Idd5 region on chromosome 1. In paper I, we provide evidence that defective upregulation of the CTLA-4 in NOD T cells is not controlled by the Idd5.1 and Idd5.2 regions, but rather by genes linked to the telomeric region of chromosome 1 and to the Idd3 locus, for which the prime candidate gene is Il-2. Interestingly, we could restore some of the defective CTLA-4 expression in NOD T cells by the addition of exogenous IL-2 during T cell activation in vitro. In paper II, we show that NOD thymocytes are resistant to superantigen-mediated negative selection and that this trait is under control of the Idd5.2 region. Interestingly, it appears to operate in a T cell non-autonomous manner. In paper III, we describe a competitive advantage of NOD thymocytes to mature when they co-develop with B6 thymocytes in embryo aggregation chimeras. These results imply that defects exist in the positive/negative selection mechanisms in the NOD thymus. Apart from T cells, B cells also play an important role in the initiation of diabetes in NOD mice, probably as antigen presenting cells. In paper IV, we report that the genetic basis of an enlarged marginal zone (MZ) B cell population observed in the NOD mice is linked to the Idd9/Idd11 region. Together, these findings contribute to the dissection of the molecular mechanisms underlying diabetes pathogenesis, and shed light on the contribution of central and peripheral tolerance mechanisms to this process.

Place, publisher, year, edition, pages
Umeå: Medicinsk biovetenskap, 2006. 108 p.
Umeå University medical dissertations, ISSN 0346-6612 ; 1015
Type 1 Diabetes, NOD mouse, CTLA-4, superantigen, T cells, Idd, marginal zone B cells, embryo aggregation chimera, negative selection
National Category
Immunology in the medical area
urn:nbn:se:umu:diva-728 (URN)91-7264-006-5 (ISBN)
Public defence
2006-03-31, Betula, 6M, Norrlands Universitetssjukhuset,, Umeå, 09:00 (English)
Available from: 2006-03-14 Created: 2006-03-14 Last updated: 2009-10-15Bibliographically approved

Open Access in DiVA

No full text

Search in DiVA

By author/editor
Motta, Vinícius
By organisation
Department of Medical Biosciences
Immunology in the medical area

Search outside of DiVA

GoogleGoogle Scholar
The number of downloads is the sum of all downloads of full texts. It may include eg previous versions that are now no longer available

Total: 22 hits
ReferencesLink to record
Permanent link

Direct link