TY - JOUR
T1 - Bitter taste cells in the ventricular walls of the murine brain regulate glucose homeostasis
AU - Yu, Qiang
AU - Gamayun, Igor
AU - Wartenberg, Philipp
AU - Zhang, Qian
AU - Qiao, Sen
AU - Kusumakshi, Soumya
AU - Candlish, Sarah
AU - Götz, Viktoria
AU - Wen, Shuping
AU - Das, Debajyoti
AU - Wyatt, Amanda
AU - Wahl, Vanessa
AU - Ectors, Fabien
AU - Kattler, Kathrin
AU - Yildiz, Daniela
AU - Prevot, Vincent
AU - Schwaninger, Markus
AU - Ternier, Gaetan
AU - Giacobini, Paolo
AU - Ciofi, Philippe
AU - Müller, Timo D.
AU - Boehm, Ulrich
N1 - Publisher Copyright:
© 2023, The Author(s).
© 2023. The Author(s).
PY - 2023/3/22
Y1 - 2023/3/22
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=85150804619&partnerID=8YFLogxK
UR - https://www.mendeley.com/catalogue/fc7b509a-8929-3ed7-9b4b-c35f073fa255/
U2 - 10.1038/s41467-023-37099-3
DO - 10.1038/s41467-023-37099-3
M3 - Journal articles
C2 - 36949050
AN - SCOPUS:85150804619
SN - 1751-8628
VL - 14
SP - 1588
JO - Nature Communications
JF - Nature Communications
IS - 1
M1 - 1588
ER -