| First Author | Szabat M | Year | 2016 |
| Journal | Cell Metab | Volume | 23 |
| Issue | 1 | Pages | 179-93 |
| PubMed ID | 26626461 | Mgi Jnum | J:232741 |
| Mgi Id | MGI:5780013 | Doi | 10.1016/j.cmet.2015.10.016 |
| Citation | Szabat M, et al. (2016) Reduced Insulin Production Relieves Endoplasmic Reticulum Stress and Induces beta Cell Proliferation. Cell Metab 23(1):179-93 |
| abstractText | Pancreatic beta cells are mostly post-mitotic, but it is unclear what locks them in this state. Perturbations including uncontrolled hyperglycemia can drive beta cells into more pliable states with reduced cellular insulin levels, increased beta cell proliferation, and hormone mis-expression, but it is unknown whether reduced insulin production itself plays a role. Here, we define the effects of approximately 50% reduced insulin production in Ins1(-/-):Ins2(f/f):Pdx1Cre(ERT):mTmG mice prior to robust hyperglycemia. Transcriptome, proteome, and network analysis revealed alleviation of chronic endoplasmic reticulum (ER) stress, indicated by reduced Ddit3, Trib3, and Atf4 expression; reduced Xbp1 splicing; and reduced phospho-eIF2alpha. This state was associated with hyper-phosphorylation of Akt, which is negatively regulated by Trib3, and with cyclinD1 upregulation. Remarkably, beta cell proliferation was increased 2-fold after reduced insulin production independently of hyperglycemia. Eventually, recombined cells mis-expressed glucagon in the hyperglycemic state. We conclude that the normally high rate of insulin production suppresses beta cell proliferation in a cell-autonomous manner. |
