Proceedings of the National Academy of Sciences · 1992 · 55 citations · 40 references
Life SciencesEndocrinologyImmunologyAutoimmunityImmunogeneticsMolecular ImmunologyAutoantibodiesAutoantigensAutoimmune DiseasesDiabetes MellitusHistocompatibility AntigensMajor Histocompatibility ComplexAutoantigen IdentificationAutoreactive T Cell ResponsesIslet AutoimmunityMajor Histocompatibility Complex GenesMajor Histocompatibility Complex GeneticsPancreatic Islet CellsSelf-tolerance BreakdownSelf-tolerance Establishment
The nonobese diabetic (NOD) mouse, in which major histocompatibility complex genes may be involved in the susceptibility to diabetes, has been developed as a model of autoimmune diabetes. The NOD mouse expresses I-A-encoded class II major histocompatibility complex antigens, which differ from those of other mouse haplotypes by the presence of a serine at position 57 of the A beta chain. Identifying islet autoantigens may help elucidate the role of class II antigens in the activation of autoreactive T cells and, thus, in the development of diabetes. We have detected autoantibodies directed against a 58-kDa islet cell antigen in NOD mice but not in other strains, including lupus-prone mice. Apart from insulin-secreting cells, the 58-kDa antigen was only found to be expressed by neuroblastoma cells and was identified as peripherin, an intermediate filament protein previously characterized in well-defined neuronal populations. This autoantigen cross-reacted with I-Anod class II antigens, suggesting that it may contribute to defective self-tolerance of islet beta cells in the NOD mouse.
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