Abstract
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.
| Original language | English |
|---|---|
| Article number | 1588 |
| Journal | Nature Communications |
| Volume | 14 |
| Issue number | 1 |
| Pages (from-to) | 1588 |
| ISSN | 1751-8628 |
| DOIs | |
| Publication status | Published - 22.03.2023 |
Funding
This project was supported by the Deutsche Forschungsgemeinschaft (DFG) through grants to Ulrich Boehm (SFB/TR 152 and SFB 894) and Timo D. Müller (SBF/TR 152 and 296), European Research Council (ERC) Synergy grant no. 810331 to Vincent Prevot and Markus Schwaninger and COST action BM1105 to Ulrich Boehm, Philippe Ciofi, Paolo Giacobini and Vincent Prevot. We thank UMS2014-US41 for technical support. We acknowledge support by the DFG and Saarland University within the Open Access Publication Funding program.