Mitochondrial transfer mediates metabolic communication between beta cells and islet macrophages
Lauar de Brito MonteiroiD, Anne‐Sophie ArchambaultiD, Paula Ma, Galina SoukhatchevaiD, Derek DaiiD, Jane VelgheiD, Dorian Izerable, Majid MojibianiD, Annette E. Patterson, Ramon I. Klein GeltinkiD, Cameron Bruce Verchere
Abstract
Pancreatic islet macrophages support islet homeostasis and adapt their metabolic program in response to environmental cues, including beta cell released factors. Intercellular mitochondrial transfer is a biological process that modulates cellular responses. To test whether beta cells, which are strongly secretory, transfer mitochondria to islet macrophages, we generated mice with beta cell-specific expression of mitochondrial GFP (PhAMfloxIns1Cre). We demonstrate that beta cells transfer mitochondria to islet macrophages in vivo and in vitro. Diabetogenic stressors did not alter the frequency of mitochondrial transfer and macrophages containing beta cell-derived GFP exhibit increased protein synthesis rates. RNA-seq identified upregulation of activity-regulated cytoskeleton associated protein (Arc) in macrophages receiving beta cell-derived mitochondria, while disruption of actin cytoskeleton dynamics prevented mitochondrial transfer. Together, these findings identify mitochondrial transfer as a previously unrecognized mechanism of beta cell-macrophage communication that may contribute to islet homeostasis and immune regulation.
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