TY - JOUR
T1 - The NOD allele of the Idd5 locus on chromosome 1 mediates a non-cell-autonomous defect in negative selection of T cells
AU - Motta, Vinicius
AU - Lejon, Kristina
AU - Holmberg, Dan
N1 - Keywords: Alleles; Animals; Antigens, Viral; Bone Marrow; Chromosomes; Diabetes Mellitus, Type 1; Mice; Mice, Inbred NOD; Quantitative Trait Loci; Receptors, Antigen, T-Cell, alpha-beta; Species Specificity; Superantigens; T-Lymphocytes; Thymus Gland; Transplantation Chimera
PY - 2007
Y1 - 2007
N2 - Recent data have suggested that non-obese diabetic (NOD) mice display a defect in negative thymic selection. Using mixed bone marrow chimeras, we demonstrate that the NOD allele of the diabetes susceptibility region 5 (Idd5) locus on chromosome 1, confers defective negative selection in response to endogenous superantigens (SAg) Mtv8 and Mtv9. We generated mixed bone marrow (BM) chimeras in which the donor cells of NOD and C3H or NOD.Idd5(b10) and C3H coexist and are similarly exposed to the Mtv8 and Mtv9 SAg. Under these conditions, SAg-mediated deletion of Vbeta11+ T cells is less efficient in chimeric mice reconstituted with NOD+C3H BM, compared with chimeras reconstituted with NOD.Idd5(b10)+C3H BM. Interestingly, the observed discrepancy was not T cell autonomous but was found to be mediated by a BM derived cellular subset, and under control of a gene(s) in the Idd5 region.
AB - Recent data have suggested that non-obese diabetic (NOD) mice display a defect in negative thymic selection. Using mixed bone marrow chimeras, we demonstrate that the NOD allele of the diabetes susceptibility region 5 (Idd5) locus on chromosome 1, confers defective negative selection in response to endogenous superantigens (SAg) Mtv8 and Mtv9. We generated mixed bone marrow (BM) chimeras in which the donor cells of NOD and C3H or NOD.Idd5(b10) and C3H coexist and are similarly exposed to the Mtv8 and Mtv9 SAg. Under these conditions, SAg-mediated deletion of Vbeta11+ T cells is less efficient in chimeric mice reconstituted with NOD+C3H BM, compared with chimeras reconstituted with NOD.Idd5(b10)+C3H BM. Interestingly, the observed discrepancy was not T cell autonomous but was found to be mediated by a BM derived cellular subset, and under control of a gene(s) in the Idd5 region.
U2 - 10.1016/j.jaut.2007.03.001
DO - 10.1016/j.jaut.2007.03.001
M3 - Journal article
C2 - 17449224
SN - 0896-8411
VL - 28
SP - 216
EP - 223
JO - Journal of Autoimmunity
JF - Journal of Autoimmunity
IS - 4
ER -