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University of Dundee

Profiling the activity of GPR55 antagonists against recombinant and endogenous GPR55

Abstract

dc:description.abstract

GPR55 is a putative novel cannabinoid receptor that is capable of being activated by a subset of cannabinoid ligands and the endogenous lipid, L-α-lysophosphatidylinositol (LPI). GPR55 mRNA is expressed widely throughout the body, particularly in the brain, bone and immune tissue, and is also expressed at high levels in certain types of tumour. Understanding the physiological and pathological role of GPR55 has been challenging due to the absence of selective pharmacological tools. However, novel antagonists have recently been developed, allowing for the determination of GPR55-selective effects. The objective of the present study was to utilise molecular imaging techniques to evaluate the effectiveness of two previously published novel GPR55 antagonists on LPI-mediated GPR55 responses, in a HEK293 cell line stably expressing GPR55 (hGPR55-HEK293) and also in a prostate cancer cell line that expresses GPR55 endogenously at high levels (DU145). Antagonist effectiveness was also examined in a neuronal model of Alzheimer’s disease (AD). The effects of the antagonists on LPI-mediated calcium (Ca2+) responses and cAMP-response element-binding protein (CREB) phosphorylation were evaluated. In hGPR55-HEK293 cells, treatment with antagonists at varying concentrations did not have an effect on intracellular Ca2+ levels or alter CREB phosphorylation when applied alone. However, both inhibited increases in Ca2+ signal induced by GPR55 agonists when applied at 3 µM. Overall, this data suggests that the GPR55 antagonists are active in in vitro models that over-express GPR55. Such pharmacological tools will help to advance the research on the physiological function of GPR55.

Degree

thesis:*
Name dc:type.qualificationname
Master of Science
Level dc:type.qualificationlevel
Master's Thesis
Grantor dc:publisher.institution
University of Dundee
Year dc:date.issued
2015

Author and committee

dc:creator, dc:contributor.*
Author dc:creator
  • Haugh, Orla

Rights

Language dc:language
eng

Identifiers

dc:identifier.*
Identifier
oai:discovery.dundee.ac.uk:studenttheses/0d07d46f-384b-43b6-8e08-54e2163cd138
OAI identifier oai:identifier
oai:discovery.dundee.ac.uk:studenttheses/0d07d46f-384b-43b6-8e08-54e2163cd138

Chain of custody

source
Harvested from
University of Dundee
Base URL
discovery.dundee.ac.uk/ws/oai
Last updated
2026-07-24
Source record
OAI-PMH GetRecord
related terms
citation

Haugh, Orla. Profiling the activity of GPR55 antagonists against recombinant and endogenous GPR55. Master's Thesis thesis, University of Dundee, 2015. https://discovery.dundee.ac.uk/en/studentTheses/0d07d46f-384b-43b6-8e08-54e2163cd138