β2-Microglobulin–Deficient NOD Mice Do Not Develop Insulitis or Diabetes

Author:

Wicker Linda S1,Leiter Edward H2,Todd John A3,Renjilian Robert J4,Peterson Erin4,Fischer Paul A5,Podolin Patricia L1,Zijlstra Maarten6,Jaenisch Rudolf6,Peterson Laurence B4

Affiliation:

1. Departments of Autoimmune Diseases Research, Merck Research Laboratories Rahway, New Jersey

2. The Jackson Laboratory Bar Harbor, Maine

3. Nuffield Department of Surgery, University of Oxford, John Radcliffe Hospital Headington, Oxford, United Kingdom

4. Cellular and Molecular Pharmacology, Merck Research Laboratories Rahway, New Jersey

5. Immunology Research, Merck Research Laboratories Rahway, New Jersey

6. Whitehead Institute for Biomedical Research and Department of Biology, Massachusetts Institute of Technology Cambridge, Massachusetts

Abstract

The role of CD8+ T-cells in the development of diabetes in the nonobese diabetic (NOD) mouse remains controversial. Although it is widely agreed that class II-restricted CD4+ T-cells are essential for the development of diabetes in the NOD model, some studies have suggested that CD8+ T-cells are not required for β-cell destruction. To assess the contribution of CD8+ T-cells to diabetes, we have developed a class of NOD mouse that lacks expression of βxs2-microglobulin (NOD-B2mnull). NOD-B2mnull mice, which lack both class I expression and CD8+ T-cells in the periphery, not only failed to develop diabetes but were completely devoid of insulitis. These results demonstrate an essential role for CD8+ T-cells in the initiation of the autoimmune response to β-cells in the NOD mouse.

Publisher

American Diabetes Association

Subject

Endocrinology, Diabetes and Metabolism,Internal Medicine

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