Abstract

Background In mammals, detection of ambient temperatures is mainly mediated by thermosensory neurons residing in the dorsal root ganglion (DRG) and trigeminal ganglion (TG) [1-3]. Recently, neurons in the Grueneberg ganglion (GG) of the murine nasal vestibule have been found to be activated by cool temperatures [4,5]. Unlike coolness-sensitive cells in the DRG and TG, neurons in the GG lack the TRPM8 channel [6] which is considered as a principal detector of cold [1-3]. Therefore, GG neurons are supposedly endowed with a so far unknown thermosensor. Interestingly, coolness-sensitive GG neurons express signaling elements associated with cyclic guanosine monophosphate (cGMP), including the cGMP-activated ion channel CNGA3 and receptor guanylyl cyclase-G (GC-G) [6-8]. Recent observations suggest that cGMP signaling is crucial for thermotransduction in the GG [8]. However, whether GC-G directly acts as a temperature sensor remains elusive.

Highlights

  • In mammals, detection of ambient temperatures is mainly mediated by thermosensory neurons residing in the dorsal root ganglion (DRG) and trigeminal ganglion (TG) [1,2,3]

  • We show that guanylyl cyclase-G (GC-G) is a thermosensory receptor that can be maximally stimulated by cool temperatures of about

  • * Correspondence: rbyang@ibms.sinica.edu.tw 1Institute of Biomedical Sciences, Academia Sinica, Taipei, Taiwan Full list of author information is available at the end of the article

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Summary

Introduction

Detection of ambient temperatures is mainly mediated by thermosensory neurons residing in the dorsal root ganglion (DRG) and trigeminal ganglion (TG) [1,2,3]. Materials and methods A combination of biochemical and molecular biology methods, Ca2+ imaging as well as behavioural studies comparing wild-type and GC-G-knockout mice was used to elucidate the molecular and biological function of GC-G in sensing cool temperatures.

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