Department of Molecular Genetics and Microbiology, Duke University School of Medicine, Durham, United States; Division of Gastroenterology, Department of Medicine, Duke University School of Medicine, Durham, United States
Olaf Mueller
Department of Molecular Genetics and Microbiology, Duke University School of Medicine, Durham, United States
Jennifer Bagwell
Department of Cell Biology, Duke University School of Medicine, Durham, United States
Department of Molecular Genetics and Microbiology, Duke University School of Medicine, Durham, United States; Division of Gastroenterology, Department of Medicine, Duke University School of Medicine, Durham, United States
Enteroendocrine cells (EECs) are specialized sensory cells in the intestinal epithelium that sense and transduce nutrient information. Consumption of dietary fat contributes to metabolic disorders, but EEC adaptations to high fat feeding were unknown. Here, we established a new experimental system to directly investigate EEC activity in vivo using a zebrafish reporter of EEC calcium signaling. Our results reveal that high fat feeding alters EEC morphology and converts them into a nutrient insensitive state that is coupled to endoplasmic reticulum (ER) stress. We called this novel adaptation 'EEC silencing'. Gnotobiotic studies revealed that germ-free zebrafish are resistant to high fat diet induced EEC silencing. High fat feeding altered gut microbiota composition including enrichment of Acinetobacter bacteria, and we identified an Acinetobacter strain sufficient to induce EEC silencing. These results establish a new mechanism by which dietary fat and gut microbiota modulate EEC nutrient sensing and signaling.