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溶血巴氏杆菌白细胞毒素可诱导牛白细胞在体外发生与凋亡一致的形态学变化。

Pasteurella haemolytica leukotoxin induces bovine leukocytes to undergo morphologic changes consistent with apoptosis in vitro.

作者信息

Stevens P K, 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. 1996 Jul;64(7):2687-94. doi: 10.1128/iai.64.7.2687-2694.1996.

Abstract

Infection of the bovine lung with Pasteurella haemolytica results in an acute respiratory disorder known as pneumonic pasteurellosis. One of the key virulence determinants used by this bacterium is secretion of an exotoxin that is specific for ruminant leukocytes (leukotoxin). At low concentrations, the leukotoxin can activate ruminant leukocytes, whereas at higher concentrations, it inhibits leukocyte functions and is cytolytic, presumably as a result of pore formation and subsequent membrane permeabilization. We have investigated the possibility that the activation-inhibition paradox is explained in part by leukotoxin-mediated apoptosis (i.e., activation-induced cell death) of bovine leukocytes. Incubation of bovine leukocytes with P. haemolytica leukotoxin caused marked cytoplasmic membrane blebbing (zeiosis) and chromatin condensation and margination, both of which are hallmarks of apoptosis. The observed morphologic changes in bovine leukocytes were leukotoxin dependent, because they were significantly diminished in the presence of an anti-leukotoxin monoclonal antibody. In addition, bovine leukocytes incubated with culture supernatant from a mutant strain of P. haemolytica that does not produce any detectable leukotoxin failed to exhibit the morphologic changes characteristic of cells undergoing apoptosis. These observations may represent an important mechanism by which P. haemolytica overwhelms host defenses, contributing to the fibrinous pleuropneumonia characteristic of bovine pasteurellosis.

摘要

溶血巴斯德氏菌感染牛肺会导致一种称为肺炎巴氏杆菌病的急性呼吸道疾病。这种细菌使用的关键毒力决定因素之一是分泌一种对反刍动物白细胞具有特异性的外毒素(白细胞毒素)。在低浓度时,白细胞毒素可激活反刍动物白细胞,而在高浓度时,它会抑制白细胞功能并具有细胞溶解性,这可能是由于形成孔道并随后导致膜通透性增加所致。我们研究了激活 - 抑制悖论部分是由白细胞毒素介导的牛白细胞凋亡(即激活诱导的细胞死亡)来解释的可能性。用溶血巴斯德氏菌白细胞毒素孵育牛白细胞会导致明显的细胞质膜起泡(胞质皱缩)以及染色质浓缩和边缘化,这两者都是细胞凋亡的标志。在牛白细胞中观察到的形态学变化依赖于白细胞毒素,因为在存在抗白细胞毒素单克隆抗体的情况下这些变化会显著减少。此外,用不产生任何可检测白细胞毒素的溶血巴斯德氏菌突变株的培养上清液孵育的牛白细胞未能表现出正在经历凋亡的细胞的特征性形态学变化。这些观察结果可能代表了溶血巴斯德氏菌克服宿主防御的一种重要机制,促成了牛巴氏杆菌病特有的纤维素性胸膜肺炎。

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Infect Immun. 1993 May;61(5):1715-21. doi: 10.1128/iai.61.5.1715-1721.1993.
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