[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
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.
Alexander, S. P., Christopoulos, A., Davenport, A. P., Kelly, E., Mathie, A., Peters, J. A., Veale, E. L., Armstrong, J. F., Faccenda, E., Harding, S. D., Pawson, A. J., Southan, C., Davies, J. A., Abbracchio, M. P., Alexander, W., al-Hosaini, K., Bäck, M., Barnes, N. M., Bathgate, R., … Ye, R. D. (2021). The Concise Guide to PHARMACOLOGY 2021/22: G protein-coupled receptors. British Journal of Pharmacology, 178(Suppl 1), S27–S156. https://doi.org/10.1111/bph.15538
Alexander, S. P., Fabbro, D., Kelly, E., Mathie, A., Peters, J. A., Veale, E. L., Armstrong, J. F., Faccenda, E., Harding, S. D., Pawson, A. J., Southan, C., Davies, J. A., Boison, D., Burns, K. E., Dessauer, C., Gertsch, J., Helsby, N. A., Izzo, A. A., Koesling, D., … Wong, S. S. (2021). THE CONCISE GUIDE TO PHARMACOLOGY 2021/22: Enzymes. British Journal of Pharmacology, 178(S1), S313–S411. https://doi.org/10.1111/bph.15542
Alexander, S. P., Mathie, A., Peters, J. A., Veale, E. L., Striessnig, J., Kelly, E., Armstrong, J. F., Faccenda, E., Harding, S. D., Pawson, A. J., Southan, C., Davies, J. A., Aldrich, R. W., Attali, B., Baggetta, A. M., Becirovic, E., Biel, M., Bill, R. M., Catterall, W. A., … Zhu, M. (2021). The Concise Guide to PHARMACOLOGY 2021/22: Ion channels. British Journal of Pharmacology, 178(Suppl 1), S157–S245. https://doi.org/10.1111/bph.15539
Alexander, S. P. H., Roberts, R. E., Broughton, B. R. S., Sobey, C. G., George, C. H., Stanford, S. C., Cirino, G., Docherty, J. R., Giembycz, M. A., Hoyer, D., Insel, P. A., Izzo, A. A., Ji, Y., MacEwan, D. J., Mangum, J., Wonnacott, S., & Ahluwalia, A. (2018). Goals and practicalities of immunoblotting and immunohistochemistry: A guide for submission to the British Journal of Pharmacology. British Journal of Pharmacology, 175(3), 407–411. https://doi.org/10.1111/bph.14112
Andersson, D. A., Nash, M., & Bevan, S. (2007). Modulation of the cold-activated channel TRPM8 by lysophospholipids and polyunsaturated fatty acids. The Journal of Neuroscience, 27(12), 3347–3355. https://doi.org/10.1523/JNEUROSCI.4846-06.2007
Babes, A., Fischer, M. J., Reid, G., Sauer, S. K., Zimmermann, K., & Reeh, P. W. (2010). Electrophysiological and neurochemical techniques to investigate sensory neurons in analgesia research. Methods in Molecular Biology, 617, 237–259. https://doi.org/10.1007/978-1-60327-323-7_19
Baubet, V., Le Mouellic, H., Campbell, A. K., Lucas-Meunier, E., Fossier, P., & Brulet, P. (2000). Chimeric green fluorescent protein-aequorin as bioluminescent Ca2+ reporters at the single-cell level. Proceedings of the National Academy of Sciences of the United States of America, 97(13), 7260–7265. https://doi.org/10.1073/pnas.97.13.7260
Bautista, D. M., Siemens, J., Glazer, J. M., Tsuruda, P. R., Basbaum, A. I., Stucky, C. L., Jordt, S. E., & Julius, D. (2007). The menthol receptor TRPM8 is the principal detector of environmental cold. Nature, 448(7150), 204–208. https://doi.org/10.1038/nature05910
Bavencoffe, A., Gkika, D., Kondratskyi, A., Beck, B., Borowiec, A. S., Bidaux, G., Busserolles, J., Eschalier, A., Shuba, Y., Skryma, R., & Prevarskaya, N. (2010). The transient receptor potential channel TRPM8 is inhibited via the alpha 2A adrenoreceptor signaling pathway. The Journal of Biological Chemistry, 285(13), 9410–9419. https://doi.org/10.1074/jbc.M109.069377
Brauchi, S., Orio, P., & Latorre, R. (2004). Clues to understanding cold sensation: Thermodynamics and electrophysiological analysis of the cold receptor TRPM8. Proceedings of the National Academy of Sciences of the United States of America, 101(43), 15494–15499. https://doi.org/10.1073/pnas.0406773101
Che, T. (2021). Advances in the treatment of chronic pain by targeting GPCRs. Biochemistry, 60(18), 1401–1412. https://doi.org/10.1021/acs.biochem.0c00644
Cottafava, F., Bertolotto, M., Brida di Prio, S., Moni, L., & Grossi-Bianchi, M. L. (1978). Clinical and immunological study of a case of mixed connective tissue disease (MCTD) with onset in childhood. Minerva Pediatrica, 30(24), 1927–1932.
Curtis, M. J., Alexander, S. P., Cirino, G., George, C. H., Kendall, D. A., Insel, P. A., Izzo, A. A., Ji, Y., Panettieri, R. A., Patel, H. H., Sobey, C. G., Stanford, S. C., Stanley, P., Stefanska, B., Stephens, G. J., Teixeira, M. M., Vergnolle, N., & Ahluwalia, A. (2022). Planning experiments: Updated guidance on experimental design and analysis and their reporting III. British Journal of Pharmacology, 179, 3907–3913. https://doi.org/10.1111/bph.15868
Daniels, R. L., Takashima, Y., & McKemy, D. D. (2009). Activity of the neuronal cold sensor TRPM8 is regulated by phospholipase C via the phospholipid phosphoinositol 4,5-bisphosphate. The Journal of Biological Chemistry, 284(3), 1570–1582. https://doi.org/10.1074/jbc.M807270200
De Petrocellis, L., Starowicz, K., Moriello, A. S., Vivese, M., Orlando, P., & Di Marzo, V. (2007). Regulation of transient receptor potential channels of melastatin type 8 (TRPM8): Effect of cAMP, cannabinoid CB1 receptors and endovanilloids. Experimental Cell Research, 313(9), 1911–1920. https://doi.org/10.1016/j.yexcr.2007.01.008
Dhaka, A., Earley, T. J., Watson, J., & Patapoutian, A. (2008). Visualizing cold spots: TRPM8-expressing sensory neurons and their projections. The Journal of Neuroscience, 28(3), 566–575. https://doi.org/10.1523/JNEUROSCI.3976-07.2008
Jung, M., Dourado, M., Maksymetz, J., Jacobson, A., Laufer, B. I., Baca, M., Foreman, O., Hackos, D. H., Riol-Blanco, L., & Kaminker, J. S. (2023). Cross-species transcriptomic atlas of dorsal root ganglia reveals species-specific programs for sensory function. Nature Communications, 14(1), 366. https://doi.org/10.1038/s41467-023-36014-0
Khalil, M., Babes, A., Lakra, R., Försch, S., Reeh, P. W., Wirtz, S., Becker, C., Neurath, M. F., & Engel, M. A. (2016). Transient receptor potential melastatin 8 ion channel in macrophages modulates colitis through a balance-shift in TNF-alpha and interleukin-10 production. Mucosal Immunology, 9(6), 1500–1513. https://doi.org/10.1038/mi.2016.16
Lilley, E., Stanford, S. C., Kendall, D. E., Alexander, S. P. H., Cirino, G., Docherty, J. R., George, C. H., Insel, P. A., Izzo, A. A., Ji, Y., Panettieri, R. A., Sobey, C. G., Stefanska, B., Stephens, G., Teixeira, M. M., & Ahluwalia, A. (2020). ARRIVE 2.0 and the British Journal of Pharmacology: Updated guidance for 2020. British Journal of Pharmacology, 177, 3611–3616. https://doi.org/10.1111/bph.15178
Linte, R. M., Ciobanu, C., Reid, G., & Babes, A. (2007). Desensitization of cold- and menthol-sensitive rat dorsal root ganglion neurones by inflammatory mediators. Experimental Brain Research, 178(1), 89–98. https://doi.org/10.1007/s00221-006-0712-3
Liu, B., Fan, L., Balakrishna, S., Sui, A., Morris, J. B., & Jordt, S. E. (2013). TRPM8 is the principal mediator of menthol-induced analgesia of acute and inflammatory pain. Pain, 154(10), 2169–2177. https://doi.org/10.1016/j.pain.2013.06.043
Liu, B., & Qin, F. (2005). Functional control of cold- and menthol-sensitive TRPM8 ion channels by phosphatidylinositol 4,5-bisphosphate. The Journal of Neuroscience, 25(7), 1674–1681. https://doi.org/10.1523/JNEUROSCI.3632-04.2005
Liu, F., Ruiz, M. S., Austin, D. A., & Webster, N. J. (2005). Constitutively active Gq impairs gonadotropin-releasing hormone-induced intracellular signaling and luteinizing hormone secretion in LβT2 cells. Molecular Endocrinology, 19(8), 2074–2085. https://doi.org/10.1210/me.2004-0145
McCoy, D. D., Knowlton, W. M., & McKemy, D. D. (2011). Scraping through the ice: Uncovering the role of TRPM8 in cold transduction. American Journal of Physiology. Regulatory, Integrative and Comparative Physiology, 300(6), R1278–R1287. https://doi.org/10.1152/ajpregu.00631.2010
Miggin, S. M., & Kinsella, B. T. (2002). Investigation of the mechanisms of G protein: Effector coupling by the human and mouse prostacyclin receptors. Identification of critical species-dependent differences. The Journal of Biological Chemistry, 277(30), 27053–27064. https://doi.org/10.1074/jbc.M203353200
Miggin, S. M., & Kinsella, B. T. (2018). Investigation of the mechanisms of G protein: Effector coupling by the human and mouse prostacyclin receptors. Identification of critical species-dependent differences. The Journal of Biological Chemistry, 293(31), 12285. https://doi.org/10.1074/jbc.W118.004804
Moncada, S., & Vane, J. R. (1979). The role of prostacyclin in vascular tissue. Federation Proceedings, 38(1), 66–71.
Murata, T., Ushikubi, F., Matsuoka, T., Hirata, M., Yamasaki, A., Sugimoto, Y., Ichikawa, A., Aze, Y., Tanaka, T., Yoshida, N., Ueno, A., Oh-ishi, S., & Narumiya, S. (1997). Altered pain perception and inflammatory response in mice lacking prostacyclin receptor. Nature, 388(6643), 678–682. https://doi.org/10.1038/41780
Nishimura, T., Yamamoto, T., Komuro, Y., & Hara, Y. (1995). Antiplatelet functions of a stable prostacyclin analog, SM-10906 are exerted by its inhibitory effect on inositol 1,4,5-trisphosphate production and cytosolic Ca++ increase in rat platelets stimulated by thrombin. Thrombosis Research, 79(3), 307–317. https://doi.org/10.1016/0049-3848(95)00117-a
Oida, H., Namba, T., Sugimoto, Y., Ushikubi, F., Ohishi, H., Ichikawa, A., & Narumiya, S. (1995). In situ hybridization studies of prostacyclin receptor mRNA expression in various mouse organs. British Journal of Pharmacology, 116(7), 2828–2837. https://doi.org/10.1111/j.1476-5381.1995.tb15933.x
Peng, Q., Alqahtani, S., Nasrullah, M. Z. A., & Shen, J. (2021). Functional evidence for biased inhibition of G protein signaling by YM-254890 in human coronary artery endothelial cells. European Journal of Pharmacology, 891, 173706. https://doi.org/10.1016/j.ejphar.2020.173706
Percie du Sert, N., Hurst, V., Ahluwalia, A., Alam, S., Avey, M. T., Baker, M., Browne, W. J., Clark, A., Cuthill, I. C., Dirnagl, U., Emerson, M., Garner, P., Holgate, S. T., Howells, D. W., Karp, N. A., Lazic, S. E., Lidster, K., MacCallum, C. J., Macleod, M., … Würbel, H. (2020). The ARRIVE guidelines 2.0: updated guidelines for reporting animal research. PLOS Biology, 18, e3000410. https://doi.org/10.1371/journal.pbio.3000410
Premkumar, L. S., Raisinghani, M., Pingle, S. C., Long, C., & Pimentel, F. (2005). Downregulation of transient receptor potential melastatin 8 by protein kinase C-mediated dephosphorylation. The Journal of Neuroscience, 25(49), 11322–11329. https://doi.org/10.1523/JNEUROSCI.3006-05.2005
Proudfoot, C. J., Garry, E. M., Cottrell, D. F., Rosie, R., Anderson, H., Robertson, D. C., Fleetwood-Walker, S. M., & Mitchell, R. (2006). Analgesia mediated by the TRPM8 cold receptor in chronic neuropathic pain. Current Biology, 16(16), 1591–1605. https://doi.org/10.1016/j.cub.2006.07.061
Ramachandran, R., Hyun, E., Zhao, L., Lapointe, T. K., Chapman, K., Hirota, C. L., Ghosh, S., McKemy, D. D., Vergnolle, N., Beck, P. L., Altier, C., & Hollenberg, M. D. (2013). TRPM8 activation attenuates inflammatory responses in mouse models of colitis. Proceedings of the National Academy of Sciences of the United States of America, 110(18), 7476–7481. https://doi.org/10.1073/pnas.1217431110
Reid, G., Amuzescu, B., Zech, E., & Flonta, M. L. (2001). A system for applying rapid warming or cooling stimuli to cells during patch clamp recording or ion imaging. Journal of Neuroscience Methods, 111(1), 1–8. https://doi.org/10.1016/s0165-0270(01)00416-2
Ricciotti, E., & FitzGerald, G. A. (2011). Prostaglandins and inflammation. Arteriosclerosis, Thrombosis, and Vascular Biology, 31(5), 986–1000. https://doi.org/10.1161/ATVBAHA.110.207449
Rohacs, T. (2014). Phosphoinositide regulation of TRP channels. Handbook of Experimental Pharmacology, 223, 1143–1176. https://doi.org/10.1007/978-3-319-05161-1_18
Ronchetti, S., Migliorati, G., & Delfino, D. V. (2017). Association of inflammatory mediators with pain perception. Biomedicine & Pharmacotherapy, 96, 1445–1452. https://doi.org/10.1016/j.biopha.2017.12.001
Sabnis, A. S., Reilly, C. A., Veranth, J. M., & Yost, G. S. (2008). Increased transcription of cytokine genes in human lung epithelial cells through activation of a TRPM8 variant by cold temperatures. American Journal of Physiology. Lung Cellular and Molecular Physiology, 295(1), L194–L200. https://doi.org/10.1152/ajplung.00072.2008
Sarria, I., & Gu, J. (2010). Menthol response and adaptation in nociceptive-like and nonnociceptive-like neurons: Role of protein kinases. Molecular Pain, 6, 47. https://doi.org/10.1186/1744-8069-6-47
Sherkheli, M. A., Gisselmann, G., Vogt-Eisele, A. K., Doerner, J. F., & Hatt, H. (2008). Menthol derivative WS-12 selectively activates transient receptor potential melastatin-8 (TRPM8) ion channels. Pakistan Journal of Pharmaceutical Sciences, 21(4), 370–378.
Silverman, H. A., Chen, A., Kravatz, N. L., Chavan, S. S., & Chang, E. H. (2020). Involvement of neural transient receptor potential channels in peripheral inflammation. Frontiers in Immunology, 11, 590261. https://doi.org/10.3389/fimmu.2020.590261
Smyth, E. M., Li, W. H., & FitzGerald, G. A. (1998). Phosphorylation of the prostacyclin receptor during homologous desensitization. A critical role for protein kinase c. The Journal of Biological Chemistry, 273(36), 23258–23266. https://doi.org/10.1074/jbc.273.36.23258
Veldhuis, N. A., Poole, D. P., Grace, M., McIntyre, P., & Bunnett, N. W. (2015). The G protein-coupled receptor-transient receptor potential channel axis: Molecular insights for targeting disorders of sensation and inflammation. Pharmacological Reviews, 67(1), 36–73. https://doi.org/10.1124/pr.114.009555
Wang, X. P., Yu, X., Yan, X. J., Lei, F., Chai, Y. S., Jiang, J. F., Yuan, Z. Y., Xing, D. M., & du, L. J. (2017). TRPM8 in the negative regulation of TNFalpha expression during cold stress. Scientific Reports, 7, 45155. https://doi.org/10.1038/srep45155
Woodward, D. F., Jones, R. L., & Narumiya, S. (2011). International Union of Basic and Clinical Pharmacology. LXXXIII: Classification of prostanoid receptors, updating 15 years of progress. Pharmacological Reviews, 63(3), 471–538. https://doi.org/10.1124/pr.110.003517
Zhang, C., Qin, J., Zhang, S., Zhang, N., Tan, B., Siwko, S., Zhang, Y., Wang, Q., Chen, J., Qian, M., Liu, M., & du, B. (2020). ADP/P2Y1 aggravates inflammatory bowel disease through ERK5-mediated NLRP3 inflammasome activation. Mucosal Immunology, 13(6), 931–945. https://doi.org/10.1038/s41385-020-0307-5
Zhang, X. (2019). Direct Gαq gating is the sole mechanism for TRPM8 inhibition caused by bradykinin receptor activation. Cell Reports, 27(12), 3672–3683 e3674. https://doi.org/10.1016/j.celrep.2019.05.080
Zhang, X., Mak, S., Li, L., Parra, A., Denlinger, B., Belmonte, C., & McNaughton, P. A. (2012). Direct inhibition of the cold-activated TRPM8 ion channel by Gαq. Nature Cell Biology, 14(8), 851–858. https://doi.org/10.1038/ncb2529