Local Integrin Activation in Pancreatic β Cells Targets Insulin Secretion to the Vasculature
2018
Wan Jun Gan | Oanh Hoang Do | Louise Cottle | Wei Ma | Elena Kosobrodova | Justin Cooper-White | Marcela Bilek | Peter Thorn
Summary: The extracellular matrix (ECM) critically affects β cell functions via integrin activation. But whether these ECM actions drive the spatial organization of β cells, as they do in epithelial cells, is unknown. Here, we show that within islets of Langerhans, focal adhesion activation in β cells occurs exclusively where they contact the capillary ECM (vascular face). In cultured β cells, 3D mapping shows enriched insulin granule fusion where the cells contact ECM-coated coverslips, which depends on β1 integrin receptor activation. Culture on micro-contact printed stripes of E-cadherin and fibronectin shows that β cell contact at the fibronectin stripe selectively activates focal adhesions and enriches exocytic machinery and insulin granule fusion. Culture of cells in high glucose, as a model of glucotoxicity, abolishes granule targeting. We conclude that local integrin activation targets insulin secretion to the islet capillaries. This mechanism might be important for islet function and may change in disease. : Pancreatic β cells are polarized within islets by unknown mechanisms. Gan et al. show that ECM contact at the vascular face of pancreatic β cells triggers local integrin β1-dependent focal adhesion activation, which orientates the cells and directs targeting of insulin granule fusion to this region. Keywords: Islets of Langerhans, beta cells, insulin, granules, secretion, exocytosis, integrin, extracellular matrix, focal adhesion, diabetes
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