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Evaluation of the Immunomodulatory Activity of the Chicken NK-Lysin-Derived Peptide cNK-2

机译:鸡NK-赖氨酸衍生肽cNK-2的免疫调节活性的评价。

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摘要

Chicken NK-lysin (cNK-lysin), the chicken homologue of human granulysin, is a cationic amphiphilic antimicrobial peptide (AMP) that is produced by cytotoxic T cells and natural killer cells. We previously demonstrated that cNK-lysin and cNK-2, a synthetic peptide incorporating the core α-helical region of cNK-lysin, have antimicrobial activity against apicomplexan parasites such as Eimeria spp., via membrane disruption. In addition to the antimicrobial activity of AMPs, the immunomodulatory activity of AMPs mediated by their interactions with host cells is increasingly recognized. Thus, in this study, we investigated whether cNK-lysin derived peptides modulate the immune response in the chicken macrophage cell line HD11 and in chicken primary monocytes by evaluating the induction of chemokines, anti-inflammatory properties, and activation of signalling pathways. cNK-2 induced the expression of CCL4, CCL5 and interleukin(IL)-1β in HD11 cells and CCL4 and CCL5 in primary monocytes. We also determined that cNK-2 suppresses the lipopolysaccharide-induced inflammatory response by abrogating IL-1β expression. The immunomodulatory activity of cNK-2 involves the mitogen-activated protein kinases-mediated signalling pathway, including p38, extracellular signal-regulated kinase 1/2 and c-Jun N-terminal kinases, as well as the internalization of cNK-2 into the cells. These results indicate that cNK-2 is a potential novel immunomodulating agent rather than an antimicrobial agent.
机译:鸡NK-溶素(cNK-lysin)是人颗粒溶素的鸡同源物,是一种阳离子两亲性抗菌肽(AMP),由细胞毒性T细胞和天然杀伤细胞产生。我们先前证明了cNK-lysin和cNK-2,一种融合了cNK-lysin核心α-螺旋区域的合成肽,具有通过膜破坏对apicomplexan寄生虫(如艾美球虫)的抗菌活性。除了AMPs的抗微生物活性外,由AMPs与宿主细胞相互作用介导的AMPs的免疫调节活性也得到越来越多的认识。因此,在这项研究中,我们通过评估趋化因子的诱导,抗炎特性和信号通路的活化,研究了cNK赖氨酸衍生肽是否能调节鸡巨噬细胞HD11和鸡单核细胞的免疫应答。 cNK-2诱导HD11细胞中CCL4,CCL5和白介素(IL)-1β的表达以及原代单核细胞中CCL4和CCL5的表达。我们还确定cNK-2通过消除IL-1β表达来抑制脂多糖诱导的炎症反应。 cNK-2的免疫调节活性涉及有丝分裂原激活的蛋白激酶介导的信号传导途径,包括p38,细胞外信号调节激酶1/2和c-Jun N端激酶,以及cNK-2内在化为c细胞。这些结果表明cNK-2是潜在的新型免疫调节剂而不是抗微生物剂。

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