Author:
Michau Aurélien,Lafont Chrystel,Bargi-Souza Paula,Kemkem Yasmine,Guillou Anne,Ravier Magalie A.,Bertrand Gyslaine,Varrault Annie,Fiordelisio Tatiana,Hodson David J.,Mollard Patrice,Schaeffer Marie
Abstract
Pancreatic islets are highly vascularized micro-organs ensuring whole body glucose homeostasis. Islet vascular cells play an integral part in sustaining adequate insulin release by beta cells. In particular, recent studies have demonstrated that islet pericytes regulate local blood flow velocity and are required for maintenance of beta cell maturity and function. In addition, increased metabolic demand accompanying obesity alters islet pericyte morphology. Here, we sought to explore the effects of metabolic stress on islet pericyte functional response to stimulation in a mouse model of type 2 diabetes, directly in the pancreas in vivo . We found that high fat diet induced islet pericyte hypertrophy without alterations in basal local blood flow. However, optogenetic stimulation of pericyte activity revealed impaired islet vascular responses, despite increased expression of genes encoding proteins directly or indirectly involved in cell contraction. These findings suggest that metabolic stress impinges upon islet pericyte function, which may contribute to beta cell failure during T2D.
Funder
Agence Nationale de la Recherche
Medical Research Centre
Société Francophone du Diabète
European Research Council
Diabetes UK
Subject
Endocrinology, Diabetes and Metabolism
Cited by
3 articles.
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