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The effect of PACAP administration on LPS-induced cytokine expression in the Atlantic salmon SHK-1 cell line.

Recent work has identified pituitary adenylate cyclase activating polypeptide (PACAP) as a potential antimicrobial and immune stimulating agent which may be suitable for use in aquaculture. However, its effects on teleost immunity are not well studied and may be significantly different than what has...

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Autores principales: Campbell, James Hugh, Dang, Xiaoqing, Rodríguez-Ramos, Tania, Carpio, Yamila, Estrada, Mario P., Dixon, Brian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10518582/
https://www.ncbi.nlm.nih.gov/pubmed/37753327
http://dx.doi.org/10.1016/j.fsirep.2023.100116
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author Campbell, James Hugh
Dang, Xiaoqing
Rodríguez-Ramos, Tania
Carpio, Yamila
Estrada, Mario P.
Dixon, Brian
author_facet Campbell, James Hugh
Dang, Xiaoqing
Rodríguez-Ramos, Tania
Carpio, Yamila
Estrada, Mario P.
Dixon, Brian
author_sort Campbell, James Hugh
collection PubMed
description Recent work has identified pituitary adenylate cyclase activating polypeptide (PACAP) as a potential antimicrobial and immune stimulating agent which may be suitable for use in aquaculture. However, its effects on teleost immunity are not well studied and may be significantly different than what has been observed in mammals. In this study we examined the effects of PACAP on the Atlantic salmon macrophage cell line SHK-1. PACAP was able to increase the expression of LPS-induced il-1β in at concentrations of 1 uM when administered 24h prior to LPS stimulation. Furthermore, concentrations as low as 40nM had an effect when administered both 24h prior and in tandem with LPS. PACAP was also capable of increasing the expression of il-1β and tnf-α in SHK-1 cells challenged with a low dose of heat-killed Flavobacterium columnare. We attempted to get a better understanding of the mechanism underlying this enhancement of il-1β expression by manipulating downstream signaling of PACAP with inhibitors of phosphodiesterase and phospholipase C activity. We found that inducing cAMP accumulation with phosphodiesterase inhibitors failed to recapitulate the effect of PACAP administration on LPS-mediated il-1β expression by PACAP, while use of a phospholipase C inhibitor caused a PACAP-like enhancement in LPS-mediated il-1β expression. Interestingly, the VPAC1 receptor inhibitor PG97-269, but not the PAC1 inhibitor max.d.4, also was capable of causing a PACAP-like enhancement in LPS-mediated il-1β expression. This suggests that fish do not utilize the PACAP receptors in the same manner as mammals, but that it still exerts an immunostimulatory effect that make it a good immunostimulant for use in aquaculture.
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spelling pubmed-105185822023-09-26 The effect of PACAP administration on LPS-induced cytokine expression in the Atlantic salmon SHK-1 cell line. Campbell, James Hugh Dang, Xiaoqing Rodríguez-Ramos, Tania Carpio, Yamila Estrada, Mario P. Dixon, Brian Fish Shellfish Immunol Rep Article Recent work has identified pituitary adenylate cyclase activating polypeptide (PACAP) as a potential antimicrobial and immune stimulating agent which may be suitable for use in aquaculture. However, its effects on teleost immunity are not well studied and may be significantly different than what has been observed in mammals. In this study we examined the effects of PACAP on the Atlantic salmon macrophage cell line SHK-1. PACAP was able to increase the expression of LPS-induced il-1β in at concentrations of 1 uM when administered 24h prior to LPS stimulation. Furthermore, concentrations as low as 40nM had an effect when administered both 24h prior and in tandem with LPS. PACAP was also capable of increasing the expression of il-1β and tnf-α in SHK-1 cells challenged with a low dose of heat-killed Flavobacterium columnare. We attempted to get a better understanding of the mechanism underlying this enhancement of il-1β expression by manipulating downstream signaling of PACAP with inhibitors of phosphodiesterase and phospholipase C activity. We found that inducing cAMP accumulation with phosphodiesterase inhibitors failed to recapitulate the effect of PACAP administration on LPS-mediated il-1β expression by PACAP, while use of a phospholipase C inhibitor caused a PACAP-like enhancement in LPS-mediated il-1β expression. Interestingly, the VPAC1 receptor inhibitor PG97-269, but not the PAC1 inhibitor max.d.4, also was capable of causing a PACAP-like enhancement in LPS-mediated il-1β expression. This suggests that fish do not utilize the PACAP receptors in the same manner as mammals, but that it still exerts an immunostimulatory effect that make it a good immunostimulant for use in aquaculture. Elsevier 2023-09-17 /pmc/articles/PMC10518582/ /pubmed/37753327 http://dx.doi.org/10.1016/j.fsirep.2023.100116 Text en © 2023 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Campbell, James Hugh
Dang, Xiaoqing
Rodríguez-Ramos, Tania
Carpio, Yamila
Estrada, Mario P.
Dixon, Brian
The effect of PACAP administration on LPS-induced cytokine expression in the Atlantic salmon SHK-1 cell line.
title The effect of PACAP administration on LPS-induced cytokine expression in the Atlantic salmon SHK-1 cell line.
title_full The effect of PACAP administration on LPS-induced cytokine expression in the Atlantic salmon SHK-1 cell line.
title_fullStr The effect of PACAP administration on LPS-induced cytokine expression in the Atlantic salmon SHK-1 cell line.
title_full_unstemmed The effect of PACAP administration on LPS-induced cytokine expression in the Atlantic salmon SHK-1 cell line.
title_short The effect of PACAP administration on LPS-induced cytokine expression in the Atlantic salmon SHK-1 cell line.
title_sort effect of pacap administration on lps-induced cytokine expression in the atlantic salmon shk-1 cell line.
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10518582/
https://www.ncbi.nlm.nih.gov/pubmed/37753327
http://dx.doi.org/10.1016/j.fsirep.2023.100116
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