Biology:Oxoeicosanoid receptor 1

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Short description: Protein-coding gene in the species Homo sapiens


A representation of the 3D structure of the protein myoglobin showing turquoise α-helices.
Generic protein structure example

Oxoeicosanoid receptor 1 (OXER1) also known as G-protein coupled receptor 170 (GPR170) is a protein that in humans is encoded by the OXER1 gene located on human chromosome 2p21; it is the principal receptor for the 5-Hydroxyicosatetraenoic acid family of carboxy fatty acid metabolites derived from arachidonic acid.[1][2][3] The receptor has also been termed hGPCR48, HGPCR48, and R527 but OXER1 is now its preferred designation.[4][5][6][7][8][2][9] OXER1 is a G protein-coupled receptor (GPCR) that is structurally related to the hydroxy-carboxylic acid (HCA) family of G protein-coupled receptors whose three members are HCA1 (GPR81), HCA2 (Niacin receptor 1), and HCA3 (Niacin receptor 2); OXER1 has 30.3%, 30.7%, and 30.7% amino acid sequence identity with these GPCRs, respectively.[10] It is also related (30.4% amino acid sequence identity) to the recently defined receptor, GPR31, for the hydroxyl-carboxy fatty acid 12-HETE.[10][11]

Species and tissue distribution

Orthologs of OXER1 are found in various mammalian species including opossums and several species of fish; however, mice and rats lack a clear ortholog of OXER1.[12][13] This represents an important hindrance to studies on the function of OXER1 since these two mammalian species are the most common and easiest models for investigating the in vivo functions of receptors in mammals and by extrapolation humans. Since mouse cells make and respond to members of the 5-HETE family of agonists,[14] it is most likely that mice do have a receptor that substitutes for OXER1 by mediating their responses to this agonist family. Recently, A G protein-couple receptor of the hydroxy carboxylic acid subfamily, Niacin receptor 1, has been proposed to mediate the responses of mouse tissues to 5-oxo-ETE.[15]

OXER1 is highly expressed by human white blood cells, particularly eosinophils and to a lesser extent neutrophils, basophils, and monocytes; by bronchoalveolar macrophages isolated from human bronchoalveolar lavage washings;[13] and by the human H295R adrenocortical cell line.[15] Various types of human cancer cells lines express OXER1; these include those of the prostate,[16][17][18] breast,[19][20] lung,[21][22] ovaries,[19][23] colon,[24] and pancreas.[25][26] OXER1 is also expressed by the human spleen, lung, liver, and kidney tissues.[27] The exact cell types bearing OXER1 in these tissues has not been defined.

A recent study has found that cats express the OXER1 receptor for 5-oxo-ETE, that feline leukocytes, including eosinophils, have been found to synthesize and be very highly responsive to 5-oxo-ETE, and that 5-oxo-ETE is present in the bronchoalveolar lavage fluid from cats with experimentally induced asthma; these findings suggest that the 5-oxo-ETE/OXER1 axis may play an important role in feline asthma, a common condition in this species, and that felines could serve as a useful animal model to investigate the pathophysiological role of 5-oxo-ETE in asthma and other conditions.[28]

Ligands

The OXER1 G protein-coupled receptor resembles the hydroxy carboxilic acid subfamily of G protein-coupled receptors, which besides GPR109A, niacin receptor 1, and niacin receptor 2 may include the recently defined receptor for 12-HETE, GPR31, not only in its amino acid sequence but also in the hydroxy-carboxylic acid nature of its cognate ligands.[29][30] Naturally occurring ligands for OXER1 are long chain polyunsaturated fatty acids containing either a hydroxyl (i.e. -OH) or oxo (i.e. =O, keto) residue removed by 5 carbons from each of these acid's carboxy residue.[31]

Agonists

OXER1 is known or presumed to bind and thereby be activated by the following endogenous arachidonic acid metabolites; 5-oxo-ETE>5-oxo-15-hydroxy-ETE>5-hydroperoxyicosatetraenoic acid (5-HpETE)>5-HETE>5,20-diHETE.[1][31][32][33][34][35][36] OXER1 is also activated by metabolites of other polyunsaturated fatty acids that therefore may be categorized as members of the 5-oxo-ETE family of agonists; these agonists include 5(S)-oxo-6E,8Z,11Z-eicosatrienoic acid (a 5-LO metabolite of mead acid); 5(S)-hydroxy-6E,8Z-octadecadienoic acid and 5(S)-oxo-6E,8Z-octadecadienoic acid (5-LO metabolites of sebaleic acid, i.e. 5Z,8Z-octadecadienoic acid); and 5(S)-hydroxy-6E,8Z,11Z,14Z,17Z-eicosapentaenoic and 5-oxo-6E,8Z,11Z,14Z,17Z-eicosapentaenoic acids (5-LO metabolites of the n-3 polyunsaturated fatty acid, eicosapentaenoic acid).[8]

Antagonists

5-Oxo-12(S)-hydroxy-HETE and its 8-trans isomer, 5-oxo-12(S)-hydroxy-6E,8E,11Z,14Z-eicosatetraenoic acid, and a series of synthetic mimetics of 5-oxo-ETE structure (compounds 346, S-264, S-230, Gue154, and still to be named but considerably more potent drugs than these) block the activity of 5-oxo-ETE but not other stimuli in leukocytes and are presumed to be OXER1 antagonists.[13][37]

Mechanisms of activating cells

OXE-R couples to the G protein complex Gαi-Gβγ; when bound to a 5-oxo-ETE family member, OXE-R triggers this G protein complex to dissociate into its Gαi and Gβγ components.[5][6][33][38] Gβγ appears to be the component most responsible for activating many of the signal pathways that lead to cellular functional responses.[39] Intracellular cell-activation pathways stimulated by OXER1 include those involving rises in cytosolic calcium ion levels,[32][40][41] and along with others that lead to the activation of MAPK/ERK, p38 mitogen-activated protein kinases, cytosolic Phospholipase A2, PI3K/Akt, and protein kinase C beta (i.e. PRKCB1, delta (i.e. PRKCD), epsilon (i.e. PRKCE), and zeta (i.e. PRKCZ).[7][16][25][42][43][44][45]

Function

OXER1 is activated by 5-oxo-ETE, 5-HETE, and other members of the 5-Hydroxyicosatetraenoic acid family of arachidonic acid metabolites and thereby mediates this family's stimulatory effects on cell types that are involved in mediating immunity-based inflammatory reactions such as neutrophils, monocytes, and macrophages) as well as allergic reactions such as eosinophils and basophils. It also mediates the in vitro proliferation and other pro-malignant responses of cultured prostate, breast, ovary, and kidney cancer cells to the 5-HETE family of agonists. These studies suggest that OXER1 may be involved in orchestrating inflammatory and allergic responses in humans and contribute to the growth and spread of human prostate, breast, ovary, and kidney cancers. OXER1 is responsible for steroid production response to 5-oxo-ETE by human steroidogenic cells in vitro and therefore could be involved in steroid production in humans.

To date, however, all studies have been pre-clinical; they use model systems that can suggest but not prove the contribution of OXER1 to human physiology and diseases. The most well-studied and promising area for OXER1 function is in allergic reactions. The recent development of OXER1 antagonists will help address this issue.

See also

  • Eicosanoid receptor
  • 5-Hydroxyicosatetraenoic acid and 5-oxo-eicosatetraenoic acid
  • Niacin receptor 1

References

  1. ↑ 1.0 1.1 "Identification of a novel human eicosanoid receptor coupled to G(i/o)". J. Biol. Chem. 277 (35): 31459–65. 2002. doi:10.1074/jbc.M203194200. PMID 12065583. 
  2. ↑ 2.0 2.1 "International Union of Pharmacology XLIV. Nomenclature for the oxoeicosanoid receptor". Pharmacol. Rev. 56 (1): 149–57. 2004. doi:10.1124/pr.56.1.4. PMID 15001665. 
  3. ↑ "Entrez Gene: OXER1 oxoeicosanoid (OXE) receptor 1". https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=165140. 
  4. ↑ "Receptors for the 5-oxo class of eicosanoids in neutrophils". J. Biol. Chem. 273 (49): 32535–41. 1998. doi:10.1074/jbc.273.49.32535. PMID 9829988. 
  5. ↑ 5.0 5.1 "Identification of a novel human eicosanoid receptor coupled to G(i/o)". J. Biol. Chem. 277 (35): 31459–31465. 2002. doi:10.1074/jbc.M203194200. PMID 12065583. 
  6. ↑ 6.0 6.1 "Expression and characterization of a 5-oxo-6E,8Z,11Z,14Z-eicosatetraenoic acid receptor highly expressed on human eosinophils and neutrophils". Mol. Pharmacol. 63 (3): 471–477. 2003. doi:10.1124/mol.63.3.471. PMID 12606753. 
  7. ↑ 7.0 7.1 "TG1019/OXE, a Galpha(i/o)-protein-coupled receptor, mediates 5-oxo-eicosatetraenoic acid-induced chemotaxis". Biochem. Biophys. Res. Commun. 334 (4): 987–995. 2005. doi:10.1016/j.bbrc.2005.06.191. PMID 16039985. 
  8. ↑ 8.0 8.1 "The eosinophil chemoattractant 5-oxo-ETE and the OXE receptor". Prog. Lipid Res. 52 (4): 651–665. 2013. doi:10.1016/j.plipres.2013.09.001. PMID 24056189. 
  9. ↑ "5-Oxo-eicosatetraenoic acid-induced chemotaxis: identification of a responsible receptor hGPCR48 and negative regulation by G protein G(12/13)". J. Biochem. 139 (3): 543–549. 2006. doi:10.1093/jb/mvj060. PMID 16567419. 
  10. ↑ 10.0 10.1 "International Union of Basic and Clinical Pharmacology. LXXXII: Nomenclature and Classification of Hydroxy-carboxylic Acid Receptors (GPR81, GPR109A, and GPR109B)". Pharmacological Reviews 63 (2): 269–90. Jun 2011. doi:10.1124/pr.110.003301. PMID 21454438. 
  11. ↑ "Identification of the orphan G protein-coupled receptor GPR31 as a receptor for 12-(S)-hydroxyeicosatetraenoic acid". The Journal of Biological Chemistry 286 (39): 33832–40. Sep 2011. doi:10.1074/jbc.M110.216564. PMID 21712392. 
  12. ↑ "The eosinophil chemoattractant 5-oxo-ETE and the OXE receptor". Prog. Lipid Res. 52 (4): 651–65. 2013. doi:10.1016/j.plipres.2013.09.001. PMID 24056189. 
  13. ↑ 13.0 13.1 13.2 "Biosynthesis, biological effects, and receptors of hydroxyeicosatetraenoic acids (HETEs) and oxoeicosatetraenoic acids (oxo-ETEs) derived from arachidonic acid". Biochim. Biophys. Acta 1851 (4): 340–355. 2014. doi:10.1016/j.bbalip.2014.10.008. PMID 25449650. 
  14. ↑ "Synthesis of 5-oxo-6,8,11,14-eicosatetraenoic acid and identification of novel omega-oxidized metabolites in the mouse macrophage". J. Pharmacol. Exp. Ther. 296 (2): 293–305. 2001. PMID 11160610. 
  15. ↑ 15.0 15.1 "Expression and function of OXE receptor, an eicosanoid receptor, in steroidogenic cells". Mol. Cell. Endocrinol. 371 (1–2): 71–8. 2013. doi:10.1016/j.mce.2012.11.003. PMID 23159987. 
  16. ↑ 16.0 16.1 "5(S)-Hydroxy-6,8,11,14-E,Z,Z,Z-eicosatetraenoate stimulates PC3 cell signaling and growth by a receptor-dependent mechanism". Cancer Res. 62 (23): 6817–9. 2002. PMID 12460891. 
  17. ↑ "Inhibition of arachidonate 5-lipoxygenase triggers massive apoptosis in human prostate cancer cells". Proc. Natl. Acad. Sci. U.S.A. 95 (22): 13182–13187. 1998. doi:10.1073/pnas.95.22.13182. PMID 9789062. Bibcode: 1998PNAS...9513182G. 
  18. ↑ "Serum levels of arachidonic acid metabolites change during prostate cancer progression". Prostate 74 (6): 618–627. 2014. doi:10.1002/pros.22779. PMID 24435810. 
  19. ↑ 19.0 19.1 "5-Oxo-ETE analogs and the proliferation of cancer cells". Biochim. Biophys. Acta 1736 (3): 228–236. 2005. doi:10.1016/j.bbalip.2005.08.009. PMID 16154383. 
  20. ↑ "Enhanced formation of 5-oxo-6,8,11,14-eicosatetraenoic acid by cancer cells in response to oxidative stress, docosahexaenoic acid and neutrophil-derived 5-hydroxy-6,8,11,14-eicosatetraenoic acid". Carcinogenesis 32 (6): 822–828. 2011. doi:10.1093/carcin/bgr044. PMID 21393477. 
  21. ↑ "Growth control of lung cancer by interruption of 5-lipoxygenase-mediated growth factor signaling". J. Clin. Invest. 97 (3): 806–813. 1996. doi:10.1172/JCI118480. PMID 8609238. 
  22. ↑ "HPLC quantification of 5-hydroxyeicosatetraenoic acid in human lung cancer tissues". Biomed. Chromatogr. 23 (8): 817–21. 2009. doi:10.1002/bmc.1191. PMID 19353686. 
  23. ↑ "Comparative analysis of peritoneum and tumor eicosanoids and pathways in advanced ovarian cancer". Clin. Cancer Res. 13 (19): 5736–44. 2007. doi:10.1158/1078-0432.CCR-07-0583. PMID 17908963. 
  24. ↑ "Inhibition of tumour growth by lipoxygenase inhibitors". Br. J. Cancer 74 (5): 683–687. 1996. doi:10.1038/bjc.1996.422. PMID 8795568. 
  25. ↑ 25.0 25.1 "Multiple signal pathways are involved in the mitogenic effect of 5(S)-HETE in human pancreatic cancer". Oncology 65 (4): 285–294. 2003. doi:10.1159/000074640. PMID 14707447. 
  26. ↑ "Lipoxygenase inhibitors abolish proliferation of human pancreatic cancer cells". Biochem. Biophys. Res. Commun. 261 (1): 218–23. 1999. doi:10.1006/bbrc.1999.1012. PMID 10405349. 
  27. ↑ "Biosynthesis, biological effects, and receptors of hydroxyeicosatetraenoic acids (HETEs) and oxoeicosatetraenoic acids (oxo-ETEs) derived from arachidonic acid". Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids 1851 (4): 340–355. Apr 2015. doi:10.1016/j.bbalip.2014.10.008. PMID 25449650. 
  28. ↑ "Biosynthesis and actions of 5-oxoeicosatetraenoic acid (5-oxo-ETE) on feline granulocytes". Biochem Pharmacol 96 (3): 247–55. Aug 2015. doi:10.1016/j.bcp.2015.05.009. PMID 26032638. 
  29. ↑ "GPR109A, GPR109B and GPR81, a family of hydroxy-carboxylic acid receptors". Trends Pharmacol. Sci. 30 (11): 557–62. 2009. doi:10.1016/j.tips.2009.09.001. PMID 19837462. 
  30. ↑ "International Union of Basic and Clinical Pharmacology. LXXXII: Nomenclature and Classification of Hydroxy-carboxylic Acid Receptors (GPR81, GPR109A, and GPR109B)". Pharmacol. Rev. 63 (2): 269–90. 2011. doi:10.1124/pr.110.003301. PMID 21454438. 
  31. ↑ 31.0 31.1 "Receptors for the 5-oxo class of eicosanoids in neutrophils". J. Biol. Chem. 273 (49): 32535–41. 1998. doi:10.1074/jbc.273.49.32535. PMID 9829988. 
  32. ↑ 32.0 32.1 "5-Hydroxyeicosatetraenoate promotes Ca2+ and protein kinase C mobilization in neutrophils". Biochem. Biophys. Res. Commun. 148 (2): 575–81. 1987. doi:10.1016/0006-291X(87)90915-6. PMID 3689361. 
  33. ↑ 33.0 33.1 "5-hydroxyicosatetraenoate stimulates neutrophils by a stereospecific, G protein-linked mechanism". J. Biol. Chem. 268 (20): 14708–14. 1993. doi:10.1016/S0021-9258(18)82391-2. PMID 8392058. 
  34. ↑ "Expression and characterization of a 5-oxo-6E,8Z,11Z,14Z-eicosatetraenoic acid receptor highly expressed on human eosinophils and neutrophils". Mol. Pharmacol. 63 (3): 471–7. 2003. doi:10.1124/mol.63.3.471. PMID 12606753. 
  35. ↑ "TG1019/OXE, a Galpha(i/o)-protein-coupled receptor, mediates 5-oxo-eicosatetraenoic acid-induced chemotaxis". Biochem. Biophys. Res. Commun. 334 (4): 987–95. 2005. doi:10.1016/j.bbrc.2005.06.191. PMID 16039985. 
  36. ↑ "Update on leukotriene, lipoxin and oxoeicosanoid receptors: IUPHAR Review 7". Br. J. Pharmacol. 171 (15): 3551–74. 2014. doi:10.1111/bph.12665. PMID 24588652. 
  37. ↑ "A biased non-Gαi OXE-R antagonist demonstrates that Gαi protein subunit is not directly involved in neutrophil, eosinophil, and monocyte activation by 5-oxo-ETE". J. Immunol. 192 (10): 4774–82. 2014. doi:10.4049/jimmunol.1302013. PMID 24733850. 
  38. ↑ "Receptors for the 5-oxo class of eicosanoids in neutrophils". J. Biol. Chem. 273 (49): 32535–32541. 1998. doi:10.1074/jbc.273.49.32535. PMID 9829988. 
  39. ↑ "ICAM-1: isoforms and phenotypes". J. Immunol. 192 (10): 4469–74. 2014. doi:10.4049/jimmunol.1400135. PMID 24795464. 
  40. ↑ "Stereospecific bioactions of 5-hydroxyeicosatetraenoate". FEBS Lett. 240 (1–2): 163–6. 1988. doi:10.1016/0014-5793(88)80360-0. PMID 3191990. 
  41. ↑ "5-Oxo-eicosatetraenoate, a potent human neutrophil stimulus". Biochem. Biophys. Res. Commun. 192 (1): 129–34. 1993. doi:10.1006/bbrc.1993.1391. PMID 8386504. 
  42. ↑ "5-Lipoxygenase products modulate the activity of the 85-kDa phospholipase A2 in human neutrophils". J. Biol. Chem. 270 (44): 26543–26549. 1995. doi:10.1074/jbc.270.44.26543. PMID 7592874. 
  43. ↑ "Inhibition of 5-lipoxygenase triggers apoptosis in prostate cancer cells via down-regulation of protein kinase C-epsilon". Biochim. Biophys. Acta 1813 (12): 2108–17. 2011. doi:10.1016/j.bbamcr.2011.07.015. PMID 21824498. 
  44. ↑ "OXER1, a G protein-coupled oxoeicosatetraenoid receptor, mediates the survival-promoting effects of arachidonate 5-lipoxygenase in prostate cancer cells". Cancer Lett. 336 (1): 185–95. 2013. doi:10.1016/j.canlet.2013.04.027. PMID 23643940. 
  45. ↑ "Crucial implication of protein kinase C (PKC)-delta, PKC-zeta, ERK-1/2, and p38 MAPK in migration of human asthmatic eosinophils". J. Leukoc. Biol. 85 (4): 656–63. 2009. doi:10.1189/jlb.0808492. PMID 19164129. 

Further reading

External links

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