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The endothelium at the interface between tissues and in the bloodstream.

作者信息

Speziale Pietro, Foster Timothy J, Arciola Carla Renata

机构信息

Department of Molecular Medicine, Unit of Biochemistry, University of Pavia, Pavia, Italy.

Department of Microbiology, Trinity College Dublin, Dublin, Ireland.

出版信息

Clin Microbiol Rev. 2025 Mar 13;38(1):e0009824. doi: 10.1128/cmr.00098-24. Epub 2025 Jan 14.


DOI:10.1128/cmr.00098-24
PMID:39807893
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11905367/
Abstract

SUMMARY is a major human pathogen. It can cause many types of infections, in particular bacteremia, which frequently leads to infective endocarditis, osteomyelitis, sepsis, and other debilitating diseases. The development of secondary infections is based on the bacterium's ability to associate with endothelial cells lining blood vessels. The success of endothelial colonization and infection by relies on its ability to express a wide array of cell wall-anchored and secreted virulence factors. Establishment of endothelial infection by the pathogen is a multistep process involving adhesion, invasion, extravasation, and dissemination of the bacterium into surrounding tissues. The process is dependent on the type of endothelium in different organs (tissues) and pathogenetic potential of the individual strains. In this review, we report an update on the organization of the endothelium in the vessels, the structure and function of the virulence factors of S. , and the several aspects of bacteria-endothelial cell interactions. After these sections, we will discuss recent advances in understanding the specific mechanisms of infections that develop in the heart, bone and joints, lung, and brain. Finally, we describe how neutrophils bind to endothelial cells, migrate to the site of infection to kill bacteria in the tissues, and how staphylococci counteract neutrophils' actions. Knowledge of the molecular details of -endothelial cell interactions will promote the development of new therapeutic strategies and tools to combat this formidable pathogen.

摘要

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本文引用的文献

[1]
Two codependent routes lead to high-level MRSA.

Science. 2024-11

[2]
Hyaluronic Acid-Modified Micelles of Azithromycin and Quercetin Against Infections Caused by Methicillin-Resistant .

Int J Nanomedicine. 2024

[3]
Wall Teichoic Acid Mediates Binding to Endothelial Cells via the Scavenger Receptor LOX-1.

ACS Infect Dis. 2023-11-10

[4]
Endothelial ADAM10 utilization defines a molecular pathway of vascular injury in mice with bacterial sepsis.

J Clin Invest. 2023-12-1

[5]
Bacterial invasion of the submicron osteocyte lacuna-canaliculi network (OLCN): a part of osteomyelitis disease biology.

APMIS. 2023-7

[6]
Autolysin-mediated peptidoglycan hydrolysis is required for the surface display of cell wall-anchored proteins.

Proc Natl Acad Sci U S A. 2023-3-21

[7]
Nectins and Nectin-like molecules drive vascular development and barrier function.

Angiogenesis. 2023-8

[8]
Staphylococcus aureus host interactions and adaptation.

Nat Rev Microbiol. 2023-6

[9]
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[10]
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