Gene Expression Data Mining Reveals the Involvement of GPR55 and Its Endogenous Ligands in Immune Response, Cancer, and Differentiation

G protein-coupled receptor 55 (GPR55) is a recently deorphanized lipid- and peptide-sensing receptor. Its lipidic endogenous agonists belong to lysoglycerophospholipids, with lysophosphatidylinositol (LPI) being the most studied. Peptide agonists derive from fragmentation of pituitary adenylate cycl...

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Main Authors: Artur Wnorowski, Jakub Wójcik, Maciej Maj
Format: Article
Language:English
Published: MDPI AG 2021-12-01
Series:International Journal of Molecular Sciences
Subjects:
Online Access:https://www.mdpi.com/1422-0067/22/24/13328
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author Artur Wnorowski
Jakub Wójcik
Maciej Maj
author_facet Artur Wnorowski
Jakub Wójcik
Maciej Maj
author_sort Artur Wnorowski
collection DOAJ
description G protein-coupled receptor 55 (GPR55) is a recently deorphanized lipid- and peptide-sensing receptor. Its lipidic endogenous agonists belong to lysoglycerophospholipids, with lysophosphatidylinositol (LPI) being the most studied. Peptide agonists derive from fragmentation of pituitary adenylate cyclase-activating polypeptide (PACAP). Although GPR55 and its ligands were implicated in several physiological and pathological conditions, their biological function remains unclear. Thus, the aim of the study was to conduct a large-scale re-analysis of publicly available gene expression datasets to identify physiological and pathological conditions affecting the expression of GPR55 and the production of its ligands. The study revealed that regulation of GPR55 occurs predominantly in the context of immune activation pointing towards the role of the receptor in response to pathogens and in immune cell lineage determination. Additionally, it was revealed that there is almost no overlap between the experimental conditions affecting the expression of GPR55 and those modulating agonist production. The capacity to synthesize LPI was enhanced in various types of tumors, indicating that cancer cells can hijack the motility-related activity of GPR55 to increase aggressiveness. Conditions favoring accumulation of PACAP-derived peptides were different than those for LPI and were mainly related to differentiation. This indicates a different function of the two agonist classes and possibly the existence of a signaling bias.
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spelling doaj.art-84133b072afb413fb95fc0cfc214417d2023-11-23T08:44:43ZengMDPI AGInternational Journal of Molecular Sciences1661-65961422-00672021-12-0122241332810.3390/ijms222413328Gene Expression Data Mining Reveals the Involvement of GPR55 and Its Endogenous Ligands in Immune Response, Cancer, and DifferentiationArtur Wnorowski0Jakub Wójcik1Maciej Maj2Department of Biopharmacy, Medical University of Lublin, 20-059 Lublin, PolandDepartment of Biopharmacy, Medical University of Lublin, 20-059 Lublin, PolandDepartment of Biopharmacy, Medical University of Lublin, 20-059 Lublin, PolandG protein-coupled receptor 55 (GPR55) is a recently deorphanized lipid- and peptide-sensing receptor. Its lipidic endogenous agonists belong to lysoglycerophospholipids, with lysophosphatidylinositol (LPI) being the most studied. Peptide agonists derive from fragmentation of pituitary adenylate cyclase-activating polypeptide (PACAP). Although GPR55 and its ligands were implicated in several physiological and pathological conditions, their biological function remains unclear. Thus, the aim of the study was to conduct a large-scale re-analysis of publicly available gene expression datasets to identify physiological and pathological conditions affecting the expression of GPR55 and the production of its ligands. The study revealed that regulation of GPR55 occurs predominantly in the context of immune activation pointing towards the role of the receptor in response to pathogens and in immune cell lineage determination. Additionally, it was revealed that there is almost no overlap between the experimental conditions affecting the expression of GPR55 and those modulating agonist production. The capacity to synthesize LPI was enhanced in various types of tumors, indicating that cancer cells can hijack the motility-related activity of GPR55 to increase aggressiveness. Conditions favoring accumulation of PACAP-derived peptides were different than those for LPI and were mainly related to differentiation. This indicates a different function of the two agonist classes and possibly the existence of a signaling bias.https://www.mdpi.com/1422-0067/22/24/13328RNAseq data miningputative cannabinoid receptorlysophosphatidylinositol biosynthesispeptide sensinglysophosphatidylglucoside receptorlysophospholipase bioactivity
spellingShingle Artur Wnorowski
Jakub Wójcik
Maciej Maj
Gene Expression Data Mining Reveals the Involvement of GPR55 and Its Endogenous Ligands in Immune Response, Cancer, and Differentiation
International Journal of Molecular Sciences
RNAseq data mining
putative cannabinoid receptor
lysophosphatidylinositol biosynthesis
peptide sensing
lysophosphatidylglucoside receptor
lysophospholipase bioactivity
title Gene Expression Data Mining Reveals the Involvement of GPR55 and Its Endogenous Ligands in Immune Response, Cancer, and Differentiation
title_full Gene Expression Data Mining Reveals the Involvement of GPR55 and Its Endogenous Ligands in Immune Response, Cancer, and Differentiation
title_fullStr Gene Expression Data Mining Reveals the Involvement of GPR55 and Its Endogenous Ligands in Immune Response, Cancer, and Differentiation
title_full_unstemmed Gene Expression Data Mining Reveals the Involvement of GPR55 and Its Endogenous Ligands in Immune Response, Cancer, and Differentiation
title_short Gene Expression Data Mining Reveals the Involvement of GPR55 and Its Endogenous Ligands in Immune Response, Cancer, and Differentiation
title_sort gene expression data mining reveals the involvement of gpr55 and its endogenous ligands in immune response cancer and differentiation
topic RNAseq data mining
putative cannabinoid receptor
lysophosphatidylinositol biosynthesis
peptide sensing
lysophosphatidylglucoside receptor
lysophospholipase bioactivity
url https://www.mdpi.com/1422-0067/22/24/13328
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