Protease-Activated Receptor 1 is Implicated in Irritable Bowel Syndrome Mediators-Induced Signalling to Thoracic Human Sensory Neurons

dc.contributor.author Desormeaux, Cleo
dc.contributor.author Bautzova, Tereza
dc.contributor.author Garcia-Caraballo, Sonia
dc.contributor.author Rolland, Corinne
dc.contributor.author Barbaro, Maria, Raffaella
dc.contributor.author Brierley, Stuart M
dc.contributor.author Barbara, Giovanni
dc.contributor.author Vergnolle, Nathalie
dc.contributor.author Cenac, Nicholas
dc.date.accessioned 2018-04-19T04:04:48Z
dc.date.available 2018-04-19T04:04:48Z
dc.date.issued 2018-03-15
dc.description Copyright © 2018 International Association for the Study of Pain This author accepted manuscript is made available following 12 month embargo from date of publication (April 2018) in accordance with the publisher’s archiving policy en_US
dc.description.abstract Proteases and Protease-Activated Receptors (PARs) are major mediators involved in irritable bowel syndrome (IBS). Our objectives were to decipher the expression and functionality (calcium signaling) of PARs in human dorsal root ganglia (DRG) neurons, and to define mechanisms involved in human sensory neuron signaling by IBS patient mediators. Human thoracic DRG were obtained from the national disease resource interchange. Expression of PAR1, PAR2 and PAR4 was assessed by immunohistochemistry and RT-qPCR in whole DRG or in primary cultures of isolated neurons. Calcium signaling in response to PAR agonist peptides (PAR-AP), their inactive peptides (PAR-IP), thrombin (10u/ml), supernatants from colonic biopsies of IBS patients or healthy controls (HC), with or without PAR1 or PAR4 antagonist were studied in cultured human DRG neurons. PAR1, PAR2 and PAR4 were all expressed in human DRG, respectively in 20%, 40% and 40% of the sensory neurons. PAR1-AP increased intracellular calcium concentration in a dose-dependent manner. This increase was inhibited by PAR1 antagonism. In contrast, PAR2-AP, PAR4-AP and PAR-IP did not cause calcium mobilization. PAR1-AP-induced calcium flux was significantly reduced by pre-incubation with PAR4-AP, but not with PAR2-AP. Thrombin increased calcium flux, which was inhibited by a PAR1 antagonist and increased by a PAR4 antagonist. Supernatants from colonic biopsies of IBS patients induced calcium flux in human sensory neurons compared to HC, this induction was reversed by a PAR1 antagonist. Taken together, our results highlight that PAR1 antagonism should be investigated as a new therapeutic target for IBS symptoms. en_US
dc.identifier.citation Desormeaux, C., Bautzova, T., Garcia-Caraballo, S., Rolland, C., Barbaro, M. R., Brierley, S. M., … Cenac, N. (2018). Protease-Activated Receptor 1 is Implicated in Irritable Bowel Syndrome Mediators-Induced Signalling to Thoracic Human Sensory Neurons. PAIN, 1. https:// doi.org/10.1097/j.pain.0000000000001208 en
dc.identifier.doi https://doi.org/10.1097/j.pain.0000000000001208 en
dc.identifier.issn 0304-3959
dc.identifier.uri http://hdl.handle.net/2328/37922
dc.language.iso en
dc.oaire.license.condition.license In Copyright
dc.publisher Wolters Kluwer Health, Inc en
dc.relation http://purl.org/au-research/grants/nhmrc/1083480 en
dc.relation.grantnumber NHMRC/1083480 en
dc.rights © 2018 International Association for the Study of Pain en
dc.rights.holder International Association for the Study of Pain en
dc.subject Proteases en
dc.subject Protease-Activated Receptors (PARs) en
dc.subject irritable bowel syndrome (IBS) en
dc.subject dorsal root ganglia (DRG) neurons en
dc.subject human sensory neuron signaling en
dc.title Protease-Activated Receptor 1 is Implicated in Irritable Bowel Syndrome Mediators-Induced Signalling to Thoracic Human Sensory Neurons en
dc.type Article en
local.contributor.authorOrcidLookup Brierley, Stuart M: https://orcid.org/0000-0002-2527-2905 en_US
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