GPR55 ligands promote receptor coupling to multiple signalling pathways
In: Cannabinoids, Jg. 160 (2010), Heft 3, S. 604-614
Online
academicJournal
- print, 3/4 p
Zugriff:
Background and purpose: Although GPR55 is potently activated by the endogenous lysophospholipid, L-α-lysophosphatidylinositol (LPI), it is also thought to be sensitive to a number of cannabinoid ligands, including the prototypic CB1 receptor antagonists AM251 and SR141716A (Rimonabant®). In this study we have used a range of functional assays to compare the pharmacological activity of selected cannabinoid ligands, AM251, AM281 and SR141716A with LPI in a HEK293 cell line engineered to stably express recombinant, human GPR55. Experimental approach: We evaluated Ca2+ signalling, stimulation of extracellular signal regulated kinase (ERK1/2) mitogen activated kinase MAP-kinases, induction of transcriptional regulators that are downstream of GPR55, including nuclear factor of activated T cells (NFAT), nuclear factor-κB (NF-κB) and cAMP response element binding protein (CREB), as well as receptor endocytosis. In addition, we assessed the suitability of a novel, label-free assay for GPR55 ligands that involves optical measurement of dynamic mass redistribution following receptor activation. Key results: GPR55 linked to a range of downstream signalling events and that the activity of GPR55 ligands was influenced by the functional assay employed, with differences in potency and efficacy observed. Conclusions and implications: Our data help to resolve some of the issues surrounding the pharmacology of cannabinoid ligands at GPR55 and highlight some differences in effector coupling associated with distinct GPR55 ligands.
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GPR55 ligands promote receptor coupling to multiple signalling pathways
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Autor/in / Beteiligte Person: | HENSTRIDGE, Christopher M ; BALENGA, Nariman Ab ; WALDHOER, Maria ; IRVING, Andrew J ; SCHRÖDER, Ralf ; KARGL, Julia K ; PLATZER, Wolfgang ; MARTINI, Lene ; ARTHUR, Simon ; PENMAN, June ; WHISTLER, Jennifer L ; KOSTENIS, Evi |
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Zeitschrift: | Cannabinoids, Jg. 160 (2010), Heft 3, S. 604-614 |
Veröffentlichung: | Basingstoke: Nature Publishing Group, 2010 |
Medientyp: | academicJournal |
Umfang: | print, 3/4 p |
ISSN: | 0007-1188 (print) |
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