So what do we call GPR18 now?
The further characterization of the orphan GPCR GPR18 conducted by McHugh et al. in this issue of the British Journal of Pharmacology has generated a pharmacological profile that raises some interesting questions about the nomenclature of this receptor and may also prompt some questions about the pharmacological definition of the classical cannabinoid receptors, CB1 and CB2.
This article is a commentary on McHugh et al., pp. 2414–2424 of this issue and is part of a themed section on Cannabinoids in Biology and Medicine. To view McHugh et al. visit http://dx.doi.org/10.1111/j.1476-5381.2011.01497.x. To view the other articles in this section visithttp://dx.doi.org/10.1111/bph.2012.165.issue-8. To view Part I of Cannabinoids in Biology and Medicine visithttp://dx.doi.org/10.1111/bph.2011.163.issue-7
In this issue of the British Journal of Pharmacology, the second associated with a celebration of the 80th birthday of Raphael Mechoulam, Doug McHugh, Heather Bradshaw and colleagues describe their investigations into the orphan GPCR, GPR18 (McHugh et al., 2012). They observed that N-arachidonoylglycine (NAGly, an endogenous fatty acid: amino acid conjugate; see Figure 1A), Δ9-tetrahydrocannabinol (THC, the major psychoactive component of the cannabis plant; see Figure 1A) and anandamide (AEA, an endogenous cannabinoid agonist; see Figure 1A) function as ‘full’ agonists at GPR18 expressed heterologously in HEK293 cells, as measured by phosphorylation of ERK1/2, with that rank order of potency. This leads me to pose the question: what do we call GPR18 now?
The short answer to that question, of course, is that we wait for a decision from the appropriate Nomenclature Committee of IUPHAR – the Union of Basic and Clinical Pharmacology (http://www.iuphar.org/nciuphar.html). So what options are open to them? Guidance from NC-IUPHAR suggests naming the receptor after the endogenous ligand or group of ligands. Of the ligands examined for activity at recombinant GPR18, NAGly was the most potent in the current study (McHugh et al., 2012). Is GPR18, therefore, a NAGly (or potentially a NAGly1 or NAG1) receptor?
NAGly as an endogenous entity
GPR18 was initially cloned and deorphanized from a human T-cell line in a search for novel chemokine-like receptors (Kohno et al., 2006). Using the recombinant receptor, NAGly was observed to be an agonist, with 10 µM of this lipoamino acid evoking a rapid and transient elevation of intracellular calcium ions. Additionally, NAGly evoked a concentration-dependent, pertussis toxin-sensitive inhibition of cAMP formation, with a calculated IC50 value of 20 nM (Kohno et al., 2006), similar to its potency in the McHugh et al. study. NAGly has been reported to be ineffective as an agonist at either CB1 or CB2 cannabinoid receptors (Sheskin et al., 1997; Huang et al., 2001), despite a marked structural similarity to the endogenous cannabinoid anandamide (Figure 1A). Indeed, it has been suggested that NAGly biosynthesis might involve anandamide as a precursor, with oxidation at the terminal alcohol by cytochrome c (McCue et al., 2008) or alcohol dehydrogenase (Bradshawet al., 2009). NAGly inhibits fatty acid amide hydrolase activity (Ghafouriet al., 2004) but not monoacylglycerol activity, suggesting selective impairment of amide endocannabinoid, but not glyceride endocannabinoid, hydrolysis (Ghafouri et al., 2004). It has also been suggested that NAGly is formed through the action of fatty acid amide hydrolase in ‘reverse mode’ (Bradshaw et al., 2009). NAGly is also a substrate for COX-2, producing prostaglandin conjugates of glycine (Prusakiewicz et al., 2002), although the relevance of this potential biotransformation is unclear.
Levels of NAGly in ex vivo tissues were initially observed to be highest in spinal cord and small intestine, with intermediate levels in brain and testes, and low levels in blood, spleen and heart (Huang et al., 2001). Further studies suggested that brain levels of NAGly were similar to those of AEA but appreciably lower than 2-arachidonoylglycerol a further endogenous cannabinoid agonist (Bradshaw et al., 2006). As yet, there are no reports demonstrating whether NAGly levels may be altered with pharmacological or pathological interventions.
Tissue distribution of GPR18
The original cloning of GPR18 suggested high levels of expression in man in testes and spleen (Gantz et al., 1997). An effect on immune function was suggested, with detectable levels of expression in the thymus, peripheral white blood cells and small intestine. Many other tissues appear to be devoid of GPR18 expression, including the brain, heart, lung, liver, kidney, pancreas, colon, skeletal muscle, ovary, placenta, prostate, adrenal medulla and cortex. In cultured cells, GPR18 expression has been identified in human lymphoid cells (Kohno et al., 2006), BV2 murine microglial cells (McHugh et al., 2010), metastatic melanoma (Qinet al., 2011) and now HEC-1B human endometrial cells (McHugh et al., 2012).
There appears, therefore, to be a slight disconnection between tissues expressing significant amounts of NAGly and the expression of the putative NAGly receptor, GPR18. Further work on the distribution of GPR18 and NAGly needs to be done to confirm co-localization (or not). Of course, it is quite conceivable that NAGly performs other functions apart from acting as a GPR18 agonist. NAGly was initially suggested to act as an agonist at GPR92, at the time another orphan receptor (Oh et al., 2008); however, a later study suggested that NAGly is a poor ligand at this receptor, while lysophosphatidic acid is a much more potent agonist (Williams et al., 2009). GPR92 has been re-named as the LPA5 receptor. Further suggested actions of NAGly include an inhibitory action at GlyT2/SLC6A5 glycine transporters (Wiles et al., 2006) and voltage-gated calcium channels (Barbara et al., 2009). So this may explain the discrepancy in distribution between agonist and receptor.
Is GPR18 a novel cannabinoid receptor?
McHugh et al. report that two cannabinoid agonists, AEA and THC, are full agonists at GPR18, while a further Cannabis-derived compound cannabidiol (CBD) is a low efficacy agonist (McHugh et al., 2012). Intriguingly, AEA is a partial agonist at CB1 cannabinoid receptors, as is THC (Pertwee et al., 2010). At CB2 cannabinoid receptors, both THC and AEA also have very low efficacy (Pertwee et al., 2010). CBD is a poor ligand at both CB1 and CB2 cannabinoid receptors (Pertwee et al., 2010). These data could be taken as evidence to suggest that GPR18 should be considered a third cannabinoid receptor, a suggestion considered premature only a year ago (Pertwee et al., 2010). Comparing primary sequences of putative cannabinoid receptors with CB1 and CB2cannabinoid receptors suggests very little overlap in structure between the archetypal cannabinoid receptors and GPR18 (or indeed with GPR55, GPR119, TRPV1, PPARα, PPARβ and PPARγ, see Figure 1B).
As yet, there is a single report investigating the possible action of 2-arachidonoylglycerol at GPR18, where it was reported to be ineffective (Yin et al., 2009). In counterpoint, though, it should be noted that this report suggested that NAGly was also ineffective as a GPR18 agonist. What would make the suggestion that GPR18 is a further cannabinoid receptor more compelling would be a response evoked by a cannabinoidin vivo that could be shown to be mediated by GPR18, and not CB1 or CB2 cannabinoid receptors. Although a transgenic mouse model has yet to be described in which the gpr18 gene is disrupted, a double knockout of CB1 and CB2 receptors has been described, which might well be an attractive topic for future research involving GPR18. Another fruitful area of research would be to investigate whether changes in GPR18 expression or coupling result when the classical cannabinoid receptors are disrupted.
Furthermore, the antagonist action of CBD at GPR18 described byMcHugh et al. (2012) may well cause a re-examination, if not re-evaluation, of the literature in which combinations of AEA and CBD or THC and CBD have been investigated. Additionally, McHugh et al. showed that the widely used CB1-selective antagonist AM251 was a very weak partial agonist at GPR18, with a calculated potency of approximately 100 µM. However, AM251 was able to evoke a concentration-dependent inhibition of THC-evoked responses at GPR18 with a potency in the mid-nanomolar range. Since THC and AM251 are often used in combination to suggest a role for CB1 cannabinoid receptorsin vivo, this interpretation may need to be more cautious in the future.
To return to my initial question about how we refer to GPR18, for the moment, the most pragmatic solution would be to retain the GPR18 nomenclature but to allow the cannabinoid community to foster this orphan, at least until further research allows a more definitive decision to be made.
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