When blood glucose levels rise, beta cells in pancreatic islets release insulin into the bloodstream. Insulin triggers glucose uptake in a variety of tissues including fat and muscle. Glucose and other nutrients must cross the vascular barrier to reach beta cells inside pancreatic islets. Similarly, newly released insulin must cross the blood vessels into the bloodstream to reach its target tissues.
Endothelial cells can be found on the inside of blood vessels. Vessels in the pancreatic islets form a dense network with many small pores in the endothelial cell membrane, facilitating the exchange of molecules across the vessel wall.
Small hair-like structures
Now, researchers have investigated how pancreatic islet vessel formation and function are affected by primary cilia, small hair-like structures found on beta cells and endothelial cells. Professor Per-Olof Berggren’s research group at The Rolf Luft Research Center for Diabetes and Endocrinology, the Department of Molecular Medicine and Surgery, Karolinska Institutet in Sweden and Dr. Jantje Gerdes’ research group at the Helmholtz Diabetes Research Center in Munich, Germany, have previously shown that insulin secretion is modulated by cilia on beta cells.
In the new study, the researchers examined a mouse model of Bardet-Biedl Syndrome, a disease caused by cilia dysfunction. They were able to show that when endothelial cilia are dysfunctional, the blood supply to the pancreatic islets is less efficient. Newly formed vessels have larger diameters and fewer pores that allow nutrients to pass through the vessel wall.
Less efficient at delivering glucose
“Consequently, the smallest blood vessels, the capillaries, become less efficient at delivering glucose to the beta cells,” says Yan Xiong, assistant professor at the Department of Molecular Medicine and Surgery, Karolinska Institutet and first author of the study.
Signaling via the growth factor VEGF-A was identified as a key player in this process. Endothelial cells that lack functional cilia are less sensitive to VEGF-A compared to normal endothelial cells, resulting in impaired signaling via the VEGFR2 receptor.
“In summary, we have demonstrated that primary cilia, specifically those on endothelial cells, regulate pancreatic islet vascularisation and vascular barrier function via the VEGF-A/VEGFR2 signaling pathway,” says Dr Gerdes, one of the senior authors of the study.
Novel therapeutic avenues
The formation of functional blood vessels is an important factor in transplantation therapies. Beta cell replacement therapy could potentially treat and cure type 1 diabetes, and the formation of a functional interface between beta cells and blood vessels is an important step towards longer graft survival and diabetes remission.
“This study improves the understanding of how primary cilia facilitate efficient blood vessel formation, and potentially offers novel therapeutic avenues to enable effective pancreatic islet transplantation in diabetes and possibly transplantation of other organs as well,” says Dr Berggren, the other senior author of the study.
The research was supported by DZD funding and a Marie Curie International Re-integration grant, the Swedish Research Council, the Novo Nordisk Foundation, Karolinska Institutet, the Swedish Diabetes Association, Knut and Alice Wallenberg Foundation, the Diabetes Research and Wellness Foundation, the Swedish Foundation for Strategic Research, Berth von Kantzow's Foundation, Skandia Insurance Company Ltd., the Strategic Research Programme in Diabetes at Karolinska Institutet, the European Research Council, the Stichting af Jochnick Foundation and the Family Erling-Persson Foundation.
Reference: Xiong Y, Scerbo MJ, Seelig A, et al. Islet vascularization is regulated by primary endothelial cilia via VEGF-A-dependent signaling. eLife. 2020. doi:10.7554/eLife.56914
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