Proinsulin Shares a Motif with Interleukin-1α (IL-1α) and Induces Inflammatory Cytokine via Interleukin-1 Receptor 1

• DOI: 10.1074/jbc.m116.731026
• Publication Date: 2016-05-17T02:28:41Z
• Authors: Siyoung Lee; Eunsom Kim; Hyunjhung Jhun; Jaewoo Hong; Areum Kwak; Seunghyun Jo; Suyoung Bae; Jongho Lee; Busun Kim; Jungmin Lee; Sulah Youn; Somi Kim; Miyeon Kim; Hyunwoo Kim; Youngmin Lee; Dong-Ki Choi; Yong-Sung Kim; Soohyun Kim
• Keywords: 0301 basic medicine; Mice; 03 medical and health sciences; Interleukin-1alpha; Immunology; Animals; Cytokines; Receptors, Interleukin-1; Inflammation Mediators; Cells, Cultured; Proinsulin; 3. Good health

Although it has been established that diabetes increases susceptibility to infections, the role of insulin (INS) in the immune response is unknown. Here, we investigated the immunological function of INS. Proinsulin dimer (pINSd) was a potent immune stimulus that induced inflammatory cytokines, but mature INS was unable to induce an immune response. An affinity-purified rabbit polyclonal antibody raised against mature IL-1α recognized IL-1α and pINS but failed to detect mature INS and IL-1β. Analysis of the pINS sequence revealed the existence of an INS/IL-1α motif in the C-peptide of pINS. Surprisingly, the INS/IL-1α motif was recognized by monoclonal antibody raised against IL-1α. Deleting the INS/IL-1α motif in pINSd and IL-1α changed their activities. To investigate the pINSd receptor, the reconstitution of IL-1 receptor 1 (IL-1R1) in Wish cells restored pINSd activity that was reversed by an IL-1R antagonist. These data suggested that pINSd needs IL-1R1 for inflammatory cytokine induction. Mouse embryo fibroblast cells of IL-1R1-deficient mice further confirmed that pINSd promotes immune responses through IL-1R1.