首页> 外文期刊>Journal of immunology research. >Development of a Cell-Based High-Throughput Screening Assay to Identify Porcine Host Defense Peptide-Inducing Compounds
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Development of a Cell-Based High-Throughput Screening Assay to Identify Porcine Host Defense Peptide-Inducing Compounds

机译:基于细胞的高通量筛选测定法的发展,以鉴定猪宿主防御肽诱导化合物。

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Novel alternatives to antibiotics are needed for the swine industry, given increasing restrictions on subtherapeutic use of antibiotics. Augmenting the synthesis of endogenous host defense peptides (HDPs) has emerged as a promising antibiotic-alternative approach to disease control and prevention. To facilitate the identification of HDP inducers for swine use, we developed a stable luciferase reporter cell line, IPEC-J2/PBD3-luc, through permanent integration of a luciferase reporter gene driven by a 1.1 kb porcine β-defensin 3 (PBD3) gene promoter in porcine IPEC-J2 intestinal epithelial cells. Such a stable reporter cell line was employed in a high-throughput screening of 148 epigenetic compounds and 584 natural products, resulting in the identification of 41 unique hits with a minimum strictly standardized mean difference (SSMD) value of 3.0. Among them, 13 compounds were further confirmed to give at least a 5-fold increase in the luciferase activity in the stable reporter cell line, with 12 being histone deacetylase (HDAC) inhibitors. Eight compounds were subsequently observed to be comparable to sodium butyrate in inducing PBD3 mRNA expression in parental IPEC-J2 cells in the low micromolar range. Six HDAC inhibitors including suberoylanilide hydroxamine (SAHA), HC toxin, apicidin, panobinostat, SB939, and LAQ824 were additionally found to be highly effective HDP inducers in a porcine 3D4/31 macrophage cell line. Besides PBD3, other HDP genes such as PBD2 and cathelicidins (PG1–5) were concentration-dependently induced by those compounds in both IPEC-J2 and 3D4/31 cells. Furthermore, the antibacterial activities of 3D4/31 cells were augmented following 24 h exposure to HDAC inhibitors. In conclusion, a cell-based high-throughput screening assay was developed for the discovery of porcine HDP inducers, and newly identified HDP-inducing compounds may have potential to be developed as alternatives to antibiotics for applications in swine and possibly other animal species.
机译:鉴于对亚治疗性使用抗生素的限制日益严格,养猪业需要新型的抗生素替代品。增强内源性宿主防御肽(HDPs)的合成已成为一种有前途的抗生素替代方法,用于疾病控制和预防。为了方便鉴定用于猪的HDP诱导剂,我们通过永久整合由1.1 kb猪β-防御素3(PBD3)基因驱动的萤光素酶报道基因,开发了稳定的萤光素酶报道细胞IPEC-J2 / PBD3-luc猪IPEC-J2肠上皮细胞中的启动子。这种稳定的报告细胞系用于148种表观遗传化合物和584种天然产物的高通量筛选,从而鉴定出41个唯一的命中样品,其最小严格标准化平均差(SSMD)值为3.0。其中,进一步证实了13种化合物在稳定的报告细胞系中荧光素酶活性提高了至少5倍,其中12种是组蛋白脱乙酰基酶(HDAC)抑制剂。随后观察到八个化合物在低微摩尔范围内诱导亲本IPEC-J2细胞中PBD3 mRNA表达方面与丁酸钠相当。在猪的3D4 / 31巨噬细胞细胞系中,还发现了六种HDAC抑制剂,包括亚磺酰苯胺羟胺(SAHA),HC毒素,阿哌西丁,panobinostat,SB939和LAQ824,它们是高效HDP诱导剂。除了PBD3外,IPEC-J2和3D4 / 31细胞中的这些化合物还浓度依赖性地诱导了其他HDP基因,如PBD2和cathelicidins(PG1-5)。此外,暴露于HDAC抑制剂24小时后,3D4 / 31细胞的抗菌活性增强。总之,已开发出一种基于细胞的高通量筛选测定方法,用于发现猪HDP诱导剂,新发现的诱导HDP的化合物可能有潜力被开发作为抗生素的替代品,用于猪和其他动物物种。

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