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ABSTRACT: Aim
To elucidate the molecular mechanism of cold sensing by visceral sensory endings, a side-by-side characterization of cold-sensitive (CS) neurons in adult mouse trigeminal (TG) and vagal ganglia (VG) was performed.Methods
A combination of physiological, pharmacological, molecular, and genetic tools was employed on trigeminal and vagal neurons.Results
CS neurons are more abundant in VG, and the majority co-express TRPA1. Cold-evoked responses are severely blunted in Trpa1 KO mice. In contrast, TRPM8 deletion or pharmacological TRPM8 blockade had little impact on VG cold sensitivity. In Trpm8eYFP reporter mice, VG TRPM8 expression was restricted to the rostral jugular ganglion. In vivo labeling of airway-innervating VG neurons demonstrated their enhanced
SUBMITTER: Gers-Barlag K
PROVIDER: S-EPMC12489895 | biostudies-literature | 2025 Nov
REPOSITORIES: biostudies-literature