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A novel bioassay to detect Nociceptin/Orphanin FQ release from single human polymorphonuclear cells

Nociceptin/Orphanin FQ (N/OFQ) is the endogenous opioid agonist for the N/OFQ receptor or NOP. This receptor system is involved in pain processing but also has a role in immune regulation. Indeed, polymorphonuclear cells (PMNs) express mRNA for N/OFQ precursor and are a potential source for circulat...

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Autores principales: Bird, M. F., Hebbes, C. P., Scott, S. W. M., Willets, J., Thompson, J. P., Lambert, D. G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9140256/
https://www.ncbi.nlm.nih.gov/pubmed/35622823
http://dx.doi.org/10.1371/journal.pone.0268868
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author Bird, M. F.
Hebbes, C. P.
Scott, S. W. M.
Willets, J.
Thompson, J. P.
Lambert, D. G.
author_facet Bird, M. F.
Hebbes, C. P.
Scott, S. W. M.
Willets, J.
Thompson, J. P.
Lambert, D. G.
author_sort Bird, M. F.
collection PubMed
description Nociceptin/Orphanin FQ (N/OFQ) is the endogenous opioid agonist for the N/OFQ receptor or NOP. This receptor system is involved in pain processing but also has a role in immune regulation. Indeed, polymorphonuclear cells (PMNs) express mRNA for N/OFQ precursor and are a potential source for circulating N/OFQ. Current measurements are based on ELISA and RIA techniques. In this study we have designed a bioassay to measure N/OFQ release from single PMNs. Chinese Hamster Ovary (CHO) cells transfected with the human (h) NOP receptor and Gα(iq5) chimera force receptor coupling in biosensor cells to increase intracellular Ca(2+); this can be measured with FLUO-4 dye. If isolated PMNs from healthy human volunteers are layered next to CHO(hNOPGαiq5) biosensor cells then stimulated with the chemoattractant N-formyl-methionyl-leucyl-phenylalanine (fMLP) we hypothesise that released N/OFQ will activate the biosensor. PMNs also release ATP and CHO cells express purinergic receptors coupled to elevated Ca(2+). In a system where these receptors (P2Y1, P2Y2 and P2X7) are blocked with high concentrations of PPADS and oATP, PMN stimulation with fMLP increases Ca(2+) in PMNs then shortly afterwards the biosensor cells. Our data therfore reports detection of single cell N/OFQ release from immune cells. This was absent when cells were preincubated with the selective NOP antagonist; SB-612111. Collectively this is the first description of single cell N/OFQ release. We will deploy this assay with further purified individual cell types and use this to further study the role of the N/OFQ-NOP system in disease; in particular sepsis where there is strong evidence for increased levels of N/OFQ worsening outcome.
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spelling pubmed-91402562022-05-28 A novel bioassay to detect Nociceptin/Orphanin FQ release from single human polymorphonuclear cells Bird, M. F. Hebbes, C. P. Scott, S. W. M. Willets, J. Thompson, J. P. Lambert, D. G. PLoS One Research Article Nociceptin/Orphanin FQ (N/OFQ) is the endogenous opioid agonist for the N/OFQ receptor or NOP. This receptor system is involved in pain processing but also has a role in immune regulation. Indeed, polymorphonuclear cells (PMNs) express mRNA for N/OFQ precursor and are a potential source for circulating N/OFQ. Current measurements are based on ELISA and RIA techniques. In this study we have designed a bioassay to measure N/OFQ release from single PMNs. Chinese Hamster Ovary (CHO) cells transfected with the human (h) NOP receptor and Gα(iq5) chimera force receptor coupling in biosensor cells to increase intracellular Ca(2+); this can be measured with FLUO-4 dye. If isolated PMNs from healthy human volunteers are layered next to CHO(hNOPGαiq5) biosensor cells then stimulated with the chemoattractant N-formyl-methionyl-leucyl-phenylalanine (fMLP) we hypothesise that released N/OFQ will activate the biosensor. PMNs also release ATP and CHO cells express purinergic receptors coupled to elevated Ca(2+). In a system where these receptors (P2Y1, P2Y2 and P2X7) are blocked with high concentrations of PPADS and oATP, PMN stimulation with fMLP increases Ca(2+) in PMNs then shortly afterwards the biosensor cells. Our data therfore reports detection of single cell N/OFQ release from immune cells. This was absent when cells were preincubated with the selective NOP antagonist; SB-612111. Collectively this is the first description of single cell N/OFQ release. We will deploy this assay with further purified individual cell types and use this to further study the role of the N/OFQ-NOP system in disease; in particular sepsis where there is strong evidence for increased levels of N/OFQ worsening outcome. Public Library of Science 2022-05-27 /pmc/articles/PMC9140256/ /pubmed/35622823 http://dx.doi.org/10.1371/journal.pone.0268868 Text en © 2022 Bird et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Bird, M. F.
Hebbes, C. P.
Scott, S. W. M.
Willets, J.
Thompson, J. P.
Lambert, D. G.
A novel bioassay to detect Nociceptin/Orphanin FQ release from single human polymorphonuclear cells
title A novel bioassay to detect Nociceptin/Orphanin FQ release from single human polymorphonuclear cells
title_full A novel bioassay to detect Nociceptin/Orphanin FQ release from single human polymorphonuclear cells
title_fullStr A novel bioassay to detect Nociceptin/Orphanin FQ release from single human polymorphonuclear cells
title_full_unstemmed A novel bioassay to detect Nociceptin/Orphanin FQ release from single human polymorphonuclear cells
title_short A novel bioassay to detect Nociceptin/Orphanin FQ release from single human polymorphonuclear cells
title_sort novel bioassay to detect nociceptin/orphanin fq release from single human polymorphonuclear cells
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9140256/
https://www.ncbi.nlm.nih.gov/pubmed/35622823
http://dx.doi.org/10.1371/journal.pone.0268868
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