Antinociceptive modulation by the adhesion GPCR CIRL promotes mechanosensory signal discrimination

Author:

Dannhäuser Sven12,Lux Thomas J3ORCID,Hu Chun4,Selcho Mareike12,Chen Jeremy T-C3,Ehmann Nadine12,Sachidanandan Divya12ORCID,Stopp Sarah12,Pauls Dennis12,Pawlak Matthias5,Langenhan Tobias6ORCID,Soba Peter4,Rittner Heike L3ORCID,Kittel Robert J12ORCID

Affiliation:

1. Department of Animal Physiology, Institute of Biology, Leipzig University, Leipzig, Germany

2. Carl-Ludwig-Institute for Physiology, Leipzig University, Leipzig, Germany

3. Center for Interdisciplinary Pain Medicine, Department of Anaesthesiology, University Hospital Würzburg, Würzburg, Germany

4. Neuronal Patterning and Connectivity, Center for Molecular Neurobiology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany

5. Department of Neurophysiology, Institute of Physiology, University of Würzburg, Würzburg, Germany

6. Rudolf Schönheimer Institute of Biochemistry, Division of General Biochemistry, Medical Faculty, Leipzig University, Leipzig, Germany

Abstract

Adhesion-type GPCRs (aGPCRs) participate in a vast range of physiological processes. Their frequent association with mechanosensitive functions suggests that processing of mechanical stimuli may be a common feature of this receptor family. Previously, we reported that the Drosophila aGPCR CIRL sensitizes sensory responses to gentle touch and sound by amplifying signal transduction in low-threshold mechanoreceptors (Scholz et al., 2017). Here, we show that Cirl is also expressed in high-threshold mechanical nociceptors where it adjusts nocifensive behaviour under physiological and pathological conditions. Optogenetic in vivo experiments indicate that CIRL lowers cAMP levels in both mechanosensory submodalities. However, contrasting its role in touch-sensitive neurons, CIRL dampens the response of nociceptors to mechanical stimulation. Consistent with this finding, rat nociceptors display decreased Cirl1 expression during allodynia. Thus, cAMP-downregulation by CIRL exerts opposing effects on low-threshold mechanosensors and high-threshold nociceptors. This intriguing bipolar action facilitates the separation of mechanosensory signals carrying different physiological information.

Funder

Deutsche Forschungsgemeinschaft

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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