Bitter taste cells in the ventricular walls of the murine brain regulate glucose homeostasis.
Qiang YuIgor GamayunPhilipp WartenbergQian ZhangSen QiaoSoumya KusumakshiSarah CandlishViktoria GötzShuping WenDebajyoti DasAmanda WyattVanessa WahlFabien EctorsKathrin KattlerDaniela YildizVincent PrevotMarkus SchwaningerGaëtan TernierPaolo GiacobiniPhilippe CiofiTimo Dirk MüllerUlrich BoehmPublished in: Nature communications (2023)
The median eminence (ME) is a circumventricular organ at the base of the brain that controls body homeostasis. Tanycytes are its specialized glial cells that constitute the ventricular walls and regulate different physiological states, however individual signaling pathways in these cells are incompletely understood. Here, we identify a functional tanycyte subpopulation that expresses key taste transduction genes including bitter taste receptors, the G protein gustducin and the gustatory ion channel TRPM5 (M5). M5 tanycytes have access to blood-borne cues via processes extended towards diaphragmed endothelial fenestrations in the ME and mediate bidirectional communication between the cerebrospinal fluid and blood. This subpopulation responds to metabolic signals including leptin and other hormonal cues and is transcriptionally reprogrammed upon fasting. Acute M5 tanycyte activation induces insulin secretion and acute diphtheria toxin-mediated M5 tanycyte depletion results in impaired glucose tolerance in diet-induced obese mice. We provide a cellular and molecular framework that defines how bitter taste cells in the ME integrate chemosensation with metabolism.
Keyphrases
- induced apoptosis
- cell cycle arrest
- signaling pathway
- endoplasmic reticulum stress
- heart failure
- escherichia coli
- cerebrospinal fluid
- type diabetes
- pi k akt
- insulin resistance
- gene expression
- multiple sclerosis
- adipose tissue
- blood glucose
- metabolic syndrome
- left ventricular
- palliative care
- respiratory failure
- weight loss
- blood brain barrier
- hepatitis b virus
- epithelial mesenchymal transition
- polycystic ovary syndrome
- brain injury
- single molecule