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Impaired pro-islet amyloid polypeptide processing promotes beta-cell dysfunction in diabetes and islet transplants

University of British Columbia

Soaring rates of diabetes highlight the importance of controlling this global epidemic, with an estimated 415 million people thought to be living with diabetes in 2015. The defining characteristic of diabetes is elevated fasting blood glucose levels, or hyperglycemia, which if not controlled promotes long-term complications such as neuropathy, kidney failure and damage to blood vessels. Glucose homeostasis is primarily controlled by pancreatic islets, cell clusters that mediate the endocrine functions of the pancreas. To manage circulating glucose concentrations, islet beta cells synthesize proinsulin, a peptide that undergoes proteolytic cleavage to become bioactive. In this dissertation, I examine the processing of the beta-cell protein pro-islet amyloid polypeptide (proIAPP), a propeptide that is cleaved similarly to proinsulin to form the aggregation-prone mature IAPP molecule, and determine whether impairments in the processing of this protein accelerate diabetes development. First, I generated a novel immunoassay to quantify the concentration of IAPP prohormone precursors for the first time in human circulation. Following rigorous validation of this ELISA, I demonstrated that elevated levels of the NH₂-proIAPP₁-₄₈ intermediate form are characteristic of type 1 diabetic recipients of islet transplants, and children with impaired glucose tolerance. Furthermore, I elucidated that this effect was not true for patients with established type 2 diabetes, implicating the peptide intermediate as a biomarker of diabetes onset but not a marker of the diseased state. Following this, I generated a rodent transplant model in which the loss of prohormone convertase 2 (PC2), essential for proIAPP processing in rodents, led to early islet transplant failure. Using a beta cell-specific PC2 null mouse that we generated, I also demonstrated that the loss of this enzyme in beta cells promotes earlier development of diabetes. Lastly, I was successful in establishing an in vitro islet culture model in which the overexpression of a non-cleavable proIAPP substrate leads to increased islet cell death. Altogether, the work in this dissertation highlights the importance of precise prohormone processing in the pancreatic islet, and demonstrates a role for proIAPP processing intermediates as biomarkers of diabetes and contributors to beta-cell dysfunction.

Text

2016-09-07

Attribution-NonCommercial-NoDerivatives 4.0 International

http://hdl.handle.net/2429/59064

Pathology and Laboratory Medicine

University of British Columbia

UBCV

http://creativecommons.org/licenses/by-nc-nd/4.0/