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

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DOI: 10.1016/j.fsirep.2023.100116

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Atlantic salmon; PACAP; innate immunity; immunostimulant; SHK-1; Flavobacterium columnare; cytokines

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Recent research suggests that PACAP may be a potential antimicrobial and immune stimulating agent for use in aquaculture. However, its effects on teleost immunity are not well understood. This study explored the effects of PACAP on Atlantic salmon macrophage cells and found that it increased the expression of il-1beta when administered prior to LPS stimulation. Furthermore, PACAP also increased the expression of il-1beta and tnf-alpha in cells challenged with heat-killed Flavobacterium columnare. The study also investigated the mechanism underlying the enhanced il-1beta expression and found that it was not mediated by cAMP accumulation, but rather by phospholipase C activity. These findings suggest that fish may utilize PACAP receptors differently than mammals, but PACAP still exhibits immunostimulatory effects in fish.
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-1 beta 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-1 beta and tnf-alpha in SHK1 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-1 beta 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-1 beta expression by PACAP, while use of a phospholipase C inhibitor caused a PACAP-like enhancement in LPS-mediated il-1 beta 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-1 beta 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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