Yang Mhan-Pyo, Ko In-Kyung, Kang Ji-Houn, Song Deok-Ho, Lee Geun-Shik, Jeung Eui-Bae
Laboratory of Veterinary Internal Medicine, Department of Veterinary Medicine, College of Veterinary Medicine and Research Institute of Veterinary Medicine, Chungbuk National University, Cheongju, Chungbuk 361-763, Republic of Korea.
Vet Immunol Immunopathol. 2005 Jun 15;106(1-2):129-38. doi: 10.1016/j.vetimm.2005.01.012.
Porcine PBMC derived phagocytic activity in peripheral blood polymorphonuclear cells (PMN) induced by egg white derivatives (EWD) treatment was analyzed at the protein and mRNA level. EWD alone failed to induce phagocytic activity of PMN measured by flow cytometry. But PMN phagocytosis was enhanced by culture supernatant from PBMC treated with EWD, human (h)rTNF-alpha and porcine (p)rIL-1beta, respectively. To identify this phagocytic inducing factor, the culture supernatant was partially purified by gel filtration. Only fraction 8 revealed the enhanced PMN phagocytic activity. This fraction also had a high cross-reactivity with anti-prTNF-alpha polyclonal (p)Ab but not with anti-prIL-1beta pAb, as measured by ELISA, indicating that the culture supernatant from PBMC treated with EWD was independent from IL-1beta. The enhanced PMN phagocytic activity of fraction 8 was also inhibited by anti-prTNF-alpha pAb. Both fraction 8 and hrTNF-alpha produced a single protein band between 16 and 18kDa upon analysis by sodium-dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) and Western blotting using anti-prTNF-alpha pAb, suggesting that the promoter of PMN phagocytosis is TNF-alpha, a 16-18 kDa protein produced by EWD-stimulated PBMC. Porcine TNF-alpha mRNA expression in porcine PBMC analyzed by RT-PCR was also increased by addition of EWD. This study strongly suggests that the immunoenhancing effect of EWD on the phagocytic response of porcine PMN is mediated through TNF-alpha produced by PBMC stimulated with EWD. In addition, the expression of porcine TNF-alpha on PBMC is also increased when stimulated with EWD.
在蛋白质和mRNA水平上分析了蛋清衍生物(EWD)处理诱导的猪外周血多形核细胞(PMN)中猪PBMC衍生的吞噬活性。单独的EWD未能通过流式细胞术检测到诱导PMN的吞噬活性。但是,分别用EWD、人(h)rTNF-α和猪(p)rIL-1β处理的PBMC培养上清液可增强PMN的吞噬作用。为了鉴定这种吞噬诱导因子,通过凝胶过滤对培养上清液进行了部分纯化。只有第8部分显示出增强的PMN吞噬活性。通过ELISA测量,该部分与抗prTNF-α多克隆(p)抗体具有高交叉反应性,但与抗prIL-1β p抗体没有交叉反应性,表明用EWD处理的PBMC培养上清液与IL-1β无关。第8部分增强的PMN吞噬活性也被抗prTNF-α p抗体抑制。通过十二烷基硫酸钠-聚丙烯酰胺凝胶电泳(SDS-PAGE)和使用抗prTNF-α p抗体的蛋白质印迹分析,第8部分和hrTNF-α在16至18kDa之间产生了一条单一的蛋白带,表明PMN吞噬作用的促进因子是TNF-α,一种由EWD刺激的PBMC产生的16-18kDa蛋白质。通过RT-PCR分析,添加EWD也增加了猪PBMC中猪TNF-α mRNA的表达。这项研究强烈表明,EWD对猪PMN吞噬反应的免疫增强作用是通过EWD刺激的PBMC产生的TNF-α介导的。此外,用EWD刺激时,猪PBMC上猪TNF-α的表达也会增加。