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炎性细胞因子在体外增强溶血曼氏杆菌白细胞毒素与牛外周血中性粒细胞的相互作用。

Inflammatory cytokines enhance the interaction of Mannheimia haemolytica leukotoxin with bovine peripheral blood neutrophils in vitro.

作者信息

Leite F, O'Brien S, Sylte M J, Page T, Atapattu D, Czuprynski C J

机构信息

Department of Pathobiological Sciences, School of Veterinary Medicine, University of Wisconsin, Madison 53706, USA.

出版信息

Infect Immun. 2002 Aug;70(8):4336-43. doi: 10.1128/IAI.70.8.4336-4343.2002.

Abstract

Mannheimia (Pasteurella) haemolytica A1 produces several virulence factors that play an important role in the pathogenesis of bovine pneumonic pasteurellosis. Foremost among these is a leukotoxin (LKT) that specifically kills ruminant leukocytes. Recent evidence suggests that M. haemolytica LKT binding to bovine leukocytes is mediated by the beta(2)-integrin CD11a/CD18 (lymphocyte function-associated antigen 1 [LFA-1]), which subsequently induces activation and cytolysis of these cells. Inflammatory cytokines, which are released during viral and bacterial infection, are reported to increase LFA-1 expression and conformational activation. We investigated the effects of the inflammatory cytokines interleukin-1beta (IL-1beta), tumor necrosis factor alpha (TNF-alpha), and gamma interferon (IFN-gamma) on the interaction of M. haemolytica LKT with bovine peripheral blood neutrophils (PMNs). In this study we demonstrated, by flow cytometry, that bovine PMNs increased their binding to an anti-bovine LFA-1 monoclonal antibody (BAT75A) following in vitro incubation with IL-1beta, TNF-alpha, or IFN-gamma. Incubation with cytokines also increased CD18 expression, as assessed by real-time PCR and by Western blotting. Increased LFA-1 expression by PMNs exposed to cytokines was associated with increased LKT binding and cytotoxicity. The latter represented, at least in part, enhanced PMN apoptosis, as assessed by propidium iodine staining and caspase-3 activation. The results of this study suggest that inflammatory cytokines may play an important role in enhancing the biological response of bovine PMNs to M. haemolytica LKT.

摘要

溶血曼氏杆菌(巴斯德氏菌)A1产生多种毒力因子,这些因子在牛肺巴氏杆菌病的发病机制中起重要作用。其中最重要的是一种白细胞毒素(LKT),它能特异性杀死反刍动物白细胞。最近的证据表明,溶血曼氏杆菌LKT与牛白细胞的结合是由β(2)-整合素CD11a/CD18(淋巴细胞功能相关抗原1 [LFA-1])介导的,随后诱导这些细胞的激活和细胞溶解。据报道,在病毒和细菌感染期间释放的炎性细胞因子会增加LFA-1的表达和构象激活。我们研究了炎性细胞因子白细胞介素-1β(IL-1β)、肿瘤坏死因子α(TNF-α)和γ干扰素(IFN-γ)对溶血曼氏杆菌LKT与牛外周血中性粒细胞(PMN)相互作用的影响。在本研究中,我们通过流式细胞术证明,牛PMN在与IL-1β、TNF-α或IFN-γ体外孵育后,其与抗牛LFA-1单克隆抗体(BAT75A)的结合增加。通过实时PCR和蛋白质印迹法评估,与细胞因子孵育也增加了CD18的表达。暴露于细胞因子的PMN中LFA-1表达的增加与LKT结合和细胞毒性的增加有关。后者至少部分表现为PMN凋亡增强,这通过碘化丙啶染色和半胱天冬酶-3激活来评估。本研究结果表明,炎性细胞因子可能在增强牛PMN对溶血曼氏杆菌LKT的生物学反应中起重要作用。

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