| First Author | Fan Y | Year | 2009 |
| Journal | EMBO J | Volume | 28 |
| Issue | 18 | Pages | 2812-24 |
| PubMed ID | 19680229 | Mgi Jnum | J:152798 |
| Mgi Id | MGI:4359988 | Doi | 10.1038/emboj.2009.212 |
| Citation | Fan Y, et al. (2009) Thymus-specific deletion of insulin induces autoimmune diabetes. EMBO J 28(18):2812-24 |
| abstractText | Insulin expression in the thymus has been implicated in regulating the negative selection of autoreactive T cells and in mediating the central immune tolerance towards pancreatic beta-cells. To further explore the function of this ectopic insulin expression, we knocked out the mouse Ins2 gene specifically in the Aire-expressing medullary thymic epithelial cells (mTECs), without affecting its expression in the beta-cells. When further crossed to the Ins1 knockout background, both male and female pups (designated as ID-TEC mice for insulin-deleted mTEC) developed diabetes spontaneously around 3 weeks after birth. beta-cell-specific autoimmune destruction was observed, as well as islet-specific T cell infiltration. The presence of insulin-specific effector T cells was shown using ELISPOT assays and adoptive T cell transfer experiments. Results from thymus transplantation experiments proved further that depletion of Ins2 expression in mTECs was sufficient to break central tolerance and induce anti-insulin autoimmunity. Our observations may explain the rare cases of type 1 diabetes onset in very young children carrying diabetes-resistant HLA class II alleles. ID-TEC mice could serve as a new model for studying this pathology. |
