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生物膜细胞外囊泡将念珠菌溶素递送至上皮细胞膜并诱导宿主细胞反应。

biofilm extracellular vesicles deliver candidalysin to epithelial cell membranes and induce host cell responses.

作者信息

Lee Sejeong, Tsavou Antzela, Zarnowski Robert, Pforte Rita, Allert Stefanie, Krüger Thomas, Kniemeyer Olaf, Brakhage Axel A, Bui Tam T T, Andes David R, Richardson Jonathan P, Hube Bernhard, Naglik Julian R

机构信息

Centre for Host-Microbiome Interactions, Faculty of Dentistry, Oral & Craniofacial Sciences, King's College London, London, United Kingdom.

Department of Medicine, Infectious Disease Division, School of Medicine & Public Health, University of Wisconsin-Madison, Madison, Wisconsin, USA.

出版信息

Infect Immun. 2025 May 13;93(5):e0040424. doi: 10.1128/iai.00404-24. Epub 2025 Apr 2.

Abstract

Extracellular vesicles (EVs) are heterogeneous particles encapsulated with a phospholipid bilayer membrane. EVs have evolved diverse biological functions, serving mainly as prominent mediators and regulators of cell-cell communication. This study investigated whether candidalysin, a key virulence factor in infections, is present within EVs derived from biofilms and retains activity by inducing host immune responses. We found that biofilm EVs contain candidalysin and can permeabilize planar lipid bilayer membranes in a dose-dependent manner. However, biofilm EVs were unable to damage oral epithelial cells (OECs) but were able to induce cytokine responses. Notably, EVs obtained from biofilms cultured for 24 h and 48 h exhibited differences in cargo composition and their ability to activate OECs. This study highlights the potential of biofilm EVs as a toxin delivery system during infection and identifies temporal differences in the ability of EVs to activate epithelial cells.

摘要

细胞外囊泡(EVs)是包裹在磷脂双分子层膜中的异质性颗粒。EVs具有多种生物学功能,主要作为细胞间通讯的重要介质和调节因子。本研究调查了念珠菌感染中的关键毒力因子念珠菌溶素是否存在于生物膜来源的EVs中,并通过诱导宿主免疫反应来保持活性。我们发现生物膜EVs含有念珠菌溶素,并且能够以剂量依赖的方式使平面脂质双分子层膜通透性增加。然而,生物膜EVs无法损伤口腔上皮细胞(OECs),但能够诱导细胞因子反应。值得注意的是,从培养24小时和48小时的生物膜中获得的EVs在货物组成及其激活OECs的能力方面存在差异。本研究强调了生物膜EVs在念珠菌感染期间作为毒素传递系统的潜力,并确定了EVs激活上皮细胞能力的时间差异。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a5ec/12070735/27d6b13d41b3/iai.00404-24.f001.jpg

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