Publication Date:
2016
abstract:
The arrangement of β cells within islets of Langerhans is critical for insulin release through the generation of rhythmic activity. A privileged role for individual β cells in orchestrating these responses has long been suspected, but not directly demonstrated. We show here that the β cell population in situ is operationally heterogeneous. Mapping of islet functional architecture revealed the presence of hub cells with pacemaker properties, which remain stable over recording periods of 2 to 3 hr. Using a dual optogenetic/photopharmacological strategy, silencing of hubs abolished coordinated islet responses to glucose, whereas specific stimulation restored communication patterns. Hubs were metabolically adapted and targeted by both pro-inflammatory and glucolipotoxic insults to induce widespread β cell dysfunction. Thus, the islet is wired by hubs, whose failure may contribute to type 2 diabetes mellitus.
Iris type:
1.1 Articolo in rivista
Keywords:
diabetes; imaging; insulin; islets; optogenetics; β cells; Animals; Calcium Signaling; Cell Differentiation; Computer Systems; Diabetes Mellitus; Glucose; Homeostasis; Humans; Insulin; Insulin-Secreting Cells; Light; Lipids; Metabolome; Metabolomics; Mice; Optical Phenomena; Phenotype; Species Specificity; Physiology; Molecular Biology; Cell Biology
List of contributors:
Johnston, Natalie R.; Mitchell, Ryan K.; Haythorne, Elizabeth; Pessoa, Maria Paiva; Semplici, Francesca; Ferrer, Jorge; Piemonti, Lorenzo; Marchetti, Piero; Bugliani, Marco; Bosco, Domenico; Berishvili, Ekaterine; Duncanson, Philip; Watkinson, Michael; Broichhagen, Johannes; Trauner, Dirk; Rutter, Guy A; Hodson, David J.
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