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Molecular analysis of the pathogenesis of autoimmune insulitis in NOD mice Koide Y; Kaidoh T; Nakamura M; Yoshida TOTohoku J Exp Med 1994[May]; 173 (1): 157-70Among diabetes-susceptibility genes in NOD mice, only Idd-1 has been clearly assigned: Idd-1 could be a gene complex composed of class II major histocompatibility complex (MHC) genes, I-A beta and I-E. Employing restriction fragment length polymorphism (RFLP) analysis and nucleotide sequencing, we revealed that ILI and CTS mice, which are nondiabetic but are derived from the same Jcl-ICR mice as NOD mice, share the same class II MHC genes with NOD mice suggesting that both ILI and CTS mice also possess susceptible Idd-1 genotype. This was supported by a breeding study. To compare the usage of T cell receptor (TCR) V beta genes in NOD mice with that in ILI mice, we employed quantitative reverse-transcriptase polymerase chain reaction (RT-PCR) which revealed that TCR V beta usages of these mice were indistinguishable. RT-PCR method also revealed that the V beta transcript of T cells infiltrating into pancreas of NOD mice was not restricted but was rather diverse. Since NOD and ILI mice share the same class I and II MHC antigens, we performed lymphocyte transfer experiments between these mice to examine the mechanism by which ILI mice do not develop insulitis. The results of reciprocal transfer of lymphocytes from NOD to ILI-nu/nu mice or from ILI to young NOD mice suggest that ILI mice exhibit autoantigens responsible for the development of insulitis but do not possess T cells reacting with islets. Of the diabetes-susceptibility genes, only in the case of Idd-1 is there any evidence for the identity of the gene products. ILI mice should provide more information on the products of the other diabetes-susceptibility genes of NOD mice.|Amino Acid Sequence[MESH]|Animals[MESH]|Autoimmune Diseases/*genetics/*immunology[MESH]|Base Sequence[MESH]|Cell Movement[MESH]|Diabetes Mellitus/genetics[MESH]|Gene Expression[MESH]|Genes[MESH]|Genes, MHC Class II[MESH]|Genetic Predisposition to Disease[MESH]|Inflammation[MESH]|Islets of Langerhans/*immunology[MESH]|Lymphocytes/*physiology[MESH]|Mice[MESH]|Mice, Inbred NOD[MESH]|Mice, Inbred Strains[MESH]|Molecular Probes/genetics[MESH]|Molecular Sequence Data[MESH]|Receptors, Antigen, T-Cell, alpha-beta/genetics[MESH] |
