Transcriptional Regulation of Type I Diabetes by NF-κB

Abstract

Development of type I diabetes requires coordinated expression of myriad genes responsible for the initiation and progression of the disease. Expression of these genes are regulated by a small number of transcription factors including the Rel/NF-κB family. To determine the roles of the Rel/NF-κB family in type I diabetes, we studied multiple low-dose streptozotocin-induced diabetes in mice deficient in either c-Rel or NF-κB1. We found that mice deficient in each of these NF-κB subunits were resistant to streptozotocin-induced diabetes. However, the mechanisms of the disease resistance may differ in different cases. Deficiency in c-Rel selectively reduced Th1, but not Th2 responses, whereas NF-κB1 deficiency had little effect on T cell responses to anti-CD3 stimulation. Death of dendritic cells was accelerated in the absence of NF-κB1, whereas death of macrophages and granulocytes was affected primarily by c-Rel deficiency. Furthermore, Stat-1 expression was significantly reduced in macrophages deficient in NF-κB1, but not c-Rel. These results indicate that both c-Rel and NF-κB1are essential for the development of type I diabetes and that strategies targeting each of these subunits would be effective in preventing the disease.