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Yu, Q.* ; Gamayun, I.* ; Wartenberg, P.* ; Zhang, Q. ; Qiao, S.* ; Kusumakshi, S.* ; Candlish, S.* ; Götz, V.* ; Wen, S.* ; Das, D.* ; Wyatt, A.* ; Wahl, V.* ; Ectors, F.* ; Kattler, K.* ; Yildiz, D.* ; Prévot, V.* ; Schwaninger, M.* ; Ternier, G.* ; Giacobini, P.* ; Ciofi, P.* ; Müller, T.D. ; Boehm, U.*

Bitter taste cells in the ventricular walls of the murine brain regulate glucose homeostasis.

Nat. Commun. 14:1588 (2023)
Publ. Version/Full Text DOI PMC
Open Access Gold
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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.
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Publication type Article: Journal article
Document type Scientific Article
Keywords Arcuate Nucleus; Messenger-rna; Food-intake; Tanycytes; Ablation; Protein; Mice; Expression; Plasticity; Receptors
Language english
Publication Year 2023
HGF-reported in Year 2023
ISSN (print) / ISBN 2041-1723
e-ISSN 2041-1723
Quellenangaben Volume: 14, Issue: 1, Pages: , Article Number: 1588 Supplement: ,
Publisher Nature Publishing Group
Publishing Place London
Reviewing status Peer reviewed
POF-Topic(s) 30201 - Metabolic Health
90000 - German Center for Diabetes Research
Research field(s) Helmholtz Diabetes Center
PSP Element(s) G-502200-006
G-501900-221
Grants European Research Council (ERC)
DFG and Saarland University
Deutsche Forschungsgemeinschaft (DFG)
Scopus ID 85150804619
PubMed ID 36949050
Erfassungsdatum 2023-10-06