Kim Hyeong-Mok, Ahn Changhwan, Kang Byeong-Teck, Kang Ji-Houn, Jeung Eui-Bae, Yang Mhan-Pyo
Department of Veterinary Medicine, Veterinary Medical Center and College of Veterinary Medicine, Chungbuk National University, Cheongju, Chungbuk 28644, Republic of Korea.
Department of Veterinary Medicine, Veterinary Medical Center and College of Veterinary Medicine, Chungbuk National University, Cheongju, Chungbuk 28644, Republic of Korea.
Res Vet Sci. 2018 Jun;118:413-418. doi: 10.1016/j.rvsc.2018.04.007. Epub 2018 Apr 18.
We examined the effect of fucoidan, an immune modulator, on the phagocytic capacity of porcine peripheral blood polymorphonuclear cells (PMNs) exposed to culture supernatant from lipopolysaccharide (LPS)-stimulated peripheral blood mononuclear cells (PBMCs). For this purpose, we evaluated the phagocytic capacity of porcine PMNs by flow cytometry and measured levels of tumor necrosis factor-alpha (TNF-α) protein and mRNA in porcine PBMCs by enzyme-linked immunosorbent assay (ELISA) and real time-polymerase chain reaction (PCR), respectively. Fucoidan or LPS alone did not affect the phagocytic capacity of PMNs, but phagocytosis by these cells was increased by exposure to culture supernatant from PBMCs treated with fucoidan or LPS. In particular, the culture supernatant from PBMCs treated with LPS revealed excessive phagocytosis of PMNs. This excessive phagocytic capacity was diminished by co-treatment LPS with fucoidan. Production of TNF-α mRNA and protein increased upon treatment of PBMCs with either fucoidan or LPS, but this effect was also diminished by co-treatment LPS with fucoidan. The ability of culture supernatant from PBMCs treated with LPS and/or fucoidan to increase the phagocytic capacity of PMNs was inhibited by anti-recombinant porcine TNF-α polyclonal antibody. These results suggested that fucoidan suppresses the phagocytic capacity of PMNs by modulating TNF-α production by LPS-stimulated PBMCs.
我们研究了免疫调节剂岩藻依聚糖对暴露于脂多糖(LPS)刺激的外周血单核细胞(PBMCs)培养上清液中的猪外周血多形核白细胞(PMNs)吞噬能力的影响。为此,我们通过流式细胞术评估了猪PMNs的吞噬能力,并分别通过酶联免疫吸附测定(ELISA)和实时聚合酶链反应(PCR)测量了猪PBMCs中肿瘤坏死因子-α(TNF-α)蛋白和mRNA的水平。单独使用岩藻依聚糖或LPS对PMNs的吞噬能力没有影响,但这些细胞在暴露于用岩藻依聚糖或LPS处理的PBMCs培养上清液后吞噬作用增强。特别是,用LPS处理的PBMCs培养上清液显示PMNs出现过度吞噬。LPS与岩藻依聚糖共同处理可减弱这种过度吞噬能力。用岩藻依聚糖或LPS处理PBMCs后,TNF-α mRNA和蛋白的产生增加,但LPS与岩藻依聚糖共同处理也可减弱这种作用。用LPS和/或岩藻依聚糖处理的PBMCs培养上清液增加PMNs吞噬能力的作用被抗重组猪TNF-α多克隆抗体抑制。这些结果表明,岩藻依聚糖通过调节LPS刺激的PBMCs产生TNF-α来抑制PMNs的吞噬能力。