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新型金黄色葡萄球菌分泌蛋白改变角质形成细胞增殖并在体内外引发促炎反应。

Novel Staphylococcus aureus Secreted Protein Alters Keratinocyte Proliferation and Elicits a Proinflammatory Response In Vitro and In Vivo.

作者信息

Merriman Joseph A, Klingelhutz Aloysius J, Diekema Daniel J, Leung Donald Y M, Schlievert Patrick M

机构信息

§University of Colorado, Denver, Anschutz Medical Campus, Aurora, Colorado 80045, United States.

出版信息

Biochemistry. 2015 Aug 11;54(31):4855-62. doi: 10.1021/acs.biochem.5b00523. Epub 2015 Jul 28.

Abstract

Staphylococcus aureus is a leading cause of surgical site infections that results in increased hospital stays due to the development of chronic wounds. Little is known about factors involved in S. aureus' ability to prevent wounds from healing. We discovered a novel secreted protein produced by a surgical site isolate of S. aureus that prevents keratinocyte proliferation. The protein has a molecular weight of 15.7 kDa and an isoelectric point of 8.9. The cloned and purified protein has cytotoxic and proinflammatory properties, as shown in vitro and in vivo. Potent biological effects on keratinocytes and rabbit skin suggest that this protein may play an important role in preventing re-epithelialization. Its lack of homology to known exotoxins suggests that this protein is novel, and this observation is likely to open a new field of research in S. aureus exotoxins. Due to its cytotoxic activities, we call this new protein ε-cytotoxin.

摘要

金黄色葡萄球菌是手术部位感染的主要原因,由于慢性伤口的形成导致住院时间延长。关于金黄色葡萄球菌阻止伤口愈合能力所涉及的因素,人们了解甚少。我们发现了一种由手术部位分离出的金黄色葡萄球菌产生的新型分泌蛋白,它能阻止角质形成细胞增殖。该蛋白分子量为15.7 kDa,等电点为8.9。克隆和纯化后的蛋白具有细胞毒性和促炎特性,体外和体内实验均已证实。对角质形成细胞和兔皮肤的强大生物学效应表明,这种蛋白可能在阻止再上皮化过程中发挥重要作用。它与已知外毒素缺乏同源性,表明该蛋白是新发现的,这一发现可能会开辟金黄色葡萄球菌外毒素研究的新领域。由于其细胞毒性活性,我们将这种新蛋白称为ε-细胞毒素。

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