Article (Scientific journals)
Inhibition of TRPM8 function by prostacyclin receptor agonists requires coupling to Gq/11 proteins.
Trif, Cosmin; Banica, Alexandra-Maria; Manolache, Alexandra et al.
2024In British Journal of Pharmacology, 181 (9), p. 1438 - 1451
Peer Reviewed verified by ORBi
 

Files


Full Text
British J Pharmacology - 2023 - Trif - Inhibition of TRPM8 function by prostacyclin receptor agonists requires coupling to.pdf
Publisher postprint (1.13 MB)
Download

All documents in ORBi are protected by a user license.

Send to



Details



Keywords :
TRPM8; inflammatory pain; prostacyclin; prostacyclin receptor; Receptors, Epoprostenol; Calcium; TRPM Cation Channels; Menthol; TRPM8 protein, human; TRPM8 channel-associated factor 1 protein, human; Membrane Proteins; TRPM8 protein, mouse; Animals; Mice; Humans; HEK293 Cells; Menthol/pharmacology; Pain; Inflammation; Membrane Proteins/metabolism; Calcium/metabolism; TRPM Cation Channels/metabolism; Pharmacology
Abstract :
[en] [en] BACKGROUND AND PURPOSE: The TRPM8 ion channel is involved in innocuous cold sensing and has a potent anti-inflammatory action. Its activation by lower temperature or chemical agonists such as menthol and icilin induces analgesic effects, reversing hypersensitivity and reducing chronic pain. On the other hand, prostacyclin (PGI2) enhances pain and inflammation by activating the IP receptors. Due to the critical roles of TRPM8 and IP receptors in the regulation of inflammatory pain, and considering their overlapping expression pattern, we analysed the functional interaction between human TRPM8 and IP receptors. EXPERIMENTAL APPROACH: We transiently expressed human TRPM8 channels and IP receptors in HEK293T cells and carried out intracellular calcium and cAMP measurements. Additionally, we cultured neurons from the dorsal root ganglia (DRGs) of mice and determined the increase in intracellular calcium triggered by the TRPM8 agonist, icilin, in the presence of the IP receptor agonist cicaprost, the IP receptor antagonist Cay10441, and the Gq/11 inhibitor YM254890. KEY RESULTS: Activation of IP receptors by selective agonists (cicaprost, beraprost, and iloprost) inhibited TRPM8 channel function, independently of the Gs-cAMP pathway. The potent inhibition of TRPM8 channels by IP receptor agonists involved Gq/11 coupling. These effects were also observed in neurons isolated from murine DRGs. CONCLUSIONS AND IMPLICATIONS: Our results demonstrate an unusual signalling pathway of IP receptors by coupling to Gq/11 proteins to inhibit TRPM8 channel function. This pathway may contribute to a better understanding of the role of TRPM8 channels and IP receptors in regulating pain and inflammation.
Disciplines :
Biochemistry, biophysics & molecular biology
Author, co-author :
Trif, Cosmin ;  Cell Signalling Research Group, Institute of Biochemistry of the Romanian Academy, Bucharest, Romania
Banica, Alexandra-Maria ;  Cell Signalling Research Group, Institute of Biochemistry of the Romanian Academy, Bucharest, Romania
Manolache, Alexandra;  Department of Anatomy, Physiology, and Biophysics, Faculty of Biology, University of Bucharest, Bucharest, Romania
Anghel, Sorina-Andreea  ;  Université de Liège - ULiège > Département de pharmacie > Chimie pharmaceutique ; Cell Signalling Research Group, Institute of Biochemistry of the Romanian Academy, Bucharest, Romania
Huţanu, Debora-Elena;  Department of Anatomy, Physiology, and Biophysics, Faculty of Biology, University of Bucharest, Bucharest, Romania
Stratulat, Teodora;  Cell Signalling Research Group, Institute of Biochemistry of the Romanian Academy, Bucharest, Romania ; Department of Anatomy, Physiology, and Biophysics, Faculty of Biology, University of Bucharest, Bucharest, Romania
Badea, Rodica;  Cell Signalling Research Group, Institute of Biochemistry of the Romanian Academy, Bucharest, Romania
Oprita, George;  Department of Anatomy, Physiology, and Biophysics, Faculty of Biology, University of Bucharest, Bucharest, Romania
Selescu, Tudor;  Department of Anatomy, Physiology, and Biophysics, Faculty of Biology, University of Bucharest, Bucharest, Romania
Petrescu, Stefana M;  Cell Signalling Research Group, Institute of Biochemistry of the Romanian Academy, Bucharest, Romania
Sisignano, Marco ;  Institute of Clinical Pharmacology, Pharmazentrum Frankfurt/ZAFES, University Hospital, Goethe-University, Frankfurt am Main, Germany
Offermanns, Stefan;  Max Planck Institute for Heart and Lung Research, Bad Nauheim, Germany
Babes, Alexandru ;  Department of Anatomy, Physiology, and Biophysics, Faculty of Biology, University of Bucharest, Bucharest, Romania
Tunaru, Sorin  ;  Cell Signalling Research Group, Institute of Biochemistry of the Romanian Academy, Bucharest, Romania ; Prothanor Biotech S.R.L., Bucharest, Romania
More authors (4 more) Less
 These authors have contributed equally to this work.
Language :
English
Title :
Inhibition of TRPM8 function by prostacyclin receptor agonists requires coupling to Gq/11 proteins.
Publication date :
May 2024
Journal title :
British Journal of Pharmacology
ISSN :
0007-1188
eISSN :
1476-5381
Publisher :
John Wiley and Sons Inc, England
Volume :
181
Issue :
9
Pages :
1438 - 1451
Peer reviewed :
Peer Reviewed verified by ORBi
Funding text :
This study was funded by the grant number 338PED (PN-III-P2-2.1-PED-2019-5179) from Executive Agency for Higher Education, Research, Development and Innovation Funding (UEFISCDI), Romania.
Available on ORBi :
since 13 April 2026

Statistics


Number of views
29 (0 by ULiège)
Number of downloads
37 (0 by ULiège)

Scopus citations®
 
1
Scopus citations®
without self-citations
1
OpenAlex citations
 
2

Bibliography


Similar publications



Contact ORBi