Staphylococcus aureus Proteases: Orchestrators of Skin Inflammation.

DNA and cell biology Pub Date : 2024-10-01 Epub Date: 2024-07-03 DOI:10.1089/dna.2024.0134
Sabrina N Kline, Yoshine Saito, Nathan K Archer
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Abstract

Skin homeostasis relies on a delicate balance between host proteases and protease inhibitors along with those secreted from microbial communities, as disruption to this harmony contributes to the pathogenesis of inflammatory skin disorders, including atopic dermatitis and Netherton's syndrome. In addition to being a prominent cause of skin and soft tissue infections, the gram-positive bacterium Staphylococcus aureus is a key player in inflammatory skin conditions due to its array of 10 secreted proteases. Herein we review how S. aureus proteases augment the development of inflammation in skin disorders. These mechanisms include degradation of skin barrier integrity, immune dysregulation and pruritis, and impairment of host defenses. Delineating the diverse roles of S. aureus proteases has the potential to reveal novel therapeutic strategies, such as inhibitors of proteases or their cognate target, as well as neutralizing vaccines to alleviate the burden of inflammatory skin disorders in patients.

金黄色葡萄球菌蛋白酶:皮肤炎症的协调者。
皮肤的平衡有赖于宿主蛋白酶和蛋白酶抑制剂以及微生物群落分泌的蛋白酶抑制剂之间的微妙平衡,破坏这种和谐会导致炎症性皮肤病的发病,包括特应性皮炎和奈瑟顿综合征。除了是皮肤和软组织感染的主要病因外,革兰氏阳性菌金黄色葡萄球菌还因其分泌的 10 种蛋白酶而在皮肤炎症中扮演重要角色。在此,我们回顾了金黄色葡萄球菌蛋白酶是如何促进皮肤疾病炎症发展的。这些机制包括皮肤屏障完整性退化、免疫调节失调和瘙痒症以及宿主防御功能受损。阐明金黄色葡萄球菌蛋白酶的不同作用有可能揭示新的治疗策略,如蛋白酶抑制剂或其同源靶点,以及中和疫苗,以减轻炎症性皮肤病患者的负担。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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