Our Research

Islets exist within a vast “ocean” of the exocrine pancreas. The role of the exocrine pancreas in maintaining islet function is poorly understood, but its importance is suggested by a strong association between diseases of the exocrine pancreas and diabetes. Our work in this area is focused on cystic fibrosis-related diabetes, and understanding the importance of exocrine-endocrine pancreas interactions in its development.

Interactions between pancreatic ductal epithelial cells and other cells of the exocrine and endocrine pancreas

Mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) result in cystic fibrosis and primarily affect cells with high CFTR expression. In the exocrine pancreas, ductal cells are the main CFTR-expressing cells, and their function is profoundly affected in CF. Diabetes is also incredibly common in people living with CF, but the underlying mechanisms remain unclear. We are undertaking a series of studies using cells from human donors and stem cell-based models to understand how loss of CFTR in ductal cells may impair function of β cells along with other cell types within the islet and exocrine pancreas.

Comprehensive analysis of the CF pancreas

The original description of cystic fibrosis almost 100 years ago was made based on microscopic evidence of pancreatic disease. However, our understanding of the nature of pathological changes in the CF pancreas remains incomplete. To fill this gap, we are generating the first comprehensive, unbiased dataset examining gene expression and gene regulation (snRNAseq+ATACseq) within all cell types of the CF pancreas. Our ongoing work to systematically map changes in the abundance and arrangement of cell types within the CF pancreas is another important component in clarifying the steps that lead to CF-related diabetes. Current projects include detailed mapping of the vasculature of the exocrine and endocrine pancreas which we have shown to be profoundly altered in CF.

Islets have a robust vascular supply, to allow delivery of nutrients and circulating stimuli to β cells, and deliver insulin and other islet hormones through the bloodstream to their target tissues. The main cells of the islet vasculature – microvascular endothelial cells and pericytes – also provide a range of factors that maintain β cells in a optimally functioning state. Conversely, in diabetes, the islet vasculature becomes inflamed and destabilized. Our ongoing work is aimed at understanding mechanisms that promote diabetes-induced vascular destabilization in the islet, the functional significance of this destabilization on insulin release and identification of candidate molecules that might improve or prevent islet vascular destabilization in diabetes. This work includes in vitro microvascular reconstitution assays and mouse models of diabetes-related microvascular disease.