ORISE/ORAU/USDA-ARS, School of Freshwater Sciences, University of Wisconsin-Milwaukee, Milwaukee, WI, 53204, USA.
USDA-ARS, School of Freshwater Sciences, University of Wisconsin-Milwaukee, Milwaukee, WI, 53204, USA.
Fish Shellfish Immunol. 2023 Jun;137:108756. doi: 10.1016/j.fsi.2023.108756. Epub 2023 Apr 25.
Accumulated evidence indicates that antimicrobial peptides modulate immune activities in fish. In this study, we profiled the differential expression patterns of representative immune relevant genes in an epithelial-like cell line of rainbow trout gill, RTgill-W1, in response to exposure of cecropin P1 antimicrobial peptide. RTgill-W1 cells were treated with synthetic cecropin P1 over time (0, 2, 4 and 24 h) with or without the present of lipopolysaccharide (LPS) or polyinosinic polycytidylic acid (PolyI:C). The relative abundances of each mRNA were measured by real-time quantitative PCR. The dose-response study revealed significant perturbations of mRNA levels of genes related to pro-inflammation, acute phase, surface proteins and transcription factors at 30 μM of cecropin P1. In addition, cecropin P1 altered the differential expression patterns that were induced by LPS or PolyI:C, at different time points in RTgill-W1. Overall, our results indicate that cecropin P1 exhibits pro-inflammation activity, modulate cell-cell interaction and cytokine signal transduction in rainbow trout gill cell, and may suggest a potential application of this peptide as an immune adjuvant for disease control in aquaculture.
越来越多的证据表明抗菌肽可调节鱼类的免疫活动。在这项研究中,我们分析了虹鳟鱼鳃上皮样细胞系 RTgill-W1 中代表性免疫相关基因的差异表达模式,以响应抗菌肽 cecropin P1 的暴露。用合成的 cecropin P1 处理 RTgill-W1 细胞,时间(0、2、4 和 24 h)不同,同时存在或不存在脂多糖(LPS)或聚肌胞苷酸(PolyI:C)。通过实时定量 PCR 测量每种 mRNA 的相对丰度。剂量反应研究表明,在 30 μM 的 cecropin P1 作用下,与炎症前体、急性期、表面蛋白和转录因子相关的基因的 mRNA 水平显著受到干扰。此外, Cecropin P1 在不同时间点改变了 LPS 或 PolyI:C 诱导的 RTgill-W1 中的差异表达模式。总的来说,我们的结果表明 Cecropin P1 具有促炎活性,可调节虹鳟鱼鳃细胞的细胞间相互作用和细胞因子信号转导,并可能暗示该肽作为水产养殖疾病控制的免疫佐剂的潜在应用。