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Exosomal mediators in sepsis and inflammatory organ injury: unraveling the role of exosomes in intercellular crosstalk and organ dysfunction.

作者信息

Gong Ting, Liu You-Tan, Fan Jie

机构信息

Department of Surgery, University of Pittsburgh School of Medicine, Pittsburgh, PA, 15213, USA.

Department of Anesthesiology, Shenzhen Hospital, Southern Medical University, Shenzhen, Guangzhou, 518110, China.

出版信息

Mil Med Res. 2024 Apr 22;11(1):24. doi: 10.1186/s40779-024-00527-6.


DOI:10.1186/s40779-024-00527-6
PMID:38644472
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11034107/
Abstract

Sepsis, a severe systemic inflammatory response to infection, remains a leading cause of morbidity and mortality worldwide. Exosomes, as mediators of intercellular communication, play a pivotal role in the pathogenesis of sepsis through modulating immune responses, metabolic reprogramming, coagulopathy, and organ dysfunction. This review highlights the emerging significance of exosomes in these processes. Initially, it provides an in-depth insight into exosome biogenesis and characterization, laying the groundwork for understanding their diverse and intricate functions. Subsequently, it explores the regulatory roles of exosomes in various immune cells such as neutrophils, macrophages, dendritic cells, T cells, and B cells. This analysis elucidates how exosomes are pivotal in modulating immune responses, thus contributing to the complexity of sepsis pathophysiology. Additionally, this review delves into the role of exosomes in the regulation of metabolism and subsequent organ dysfunction in sepsis. It also establishes a connection between exosomes and the coagulation cascade, which affects endothelial integrity and promotes thrombogenesis in sepsis. Moreover, the review discusses the dual role of exosomes in the progression and resolution of sepsis, exploring their complex involvement in inflammation and healing processes. Furthermore, it underscores their potential as biomarkers and therapeutic targets. Understanding these mechanisms presents new opportunities for novel interventions to mitigate the severe outcomes of sepsis, emphasizing the therapeutic promise of exosome research in critical care settings.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ac66/11034107/8640c7441fe9/40779_2024_527_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ac66/11034107/ffbf09a64e99/40779_2024_527_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ac66/11034107/c555264552b6/40779_2024_527_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ac66/11034107/8640c7441fe9/40779_2024_527_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ac66/11034107/ffbf09a64e99/40779_2024_527_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ac66/11034107/c555264552b6/40779_2024_527_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ac66/11034107/8640c7441fe9/40779_2024_527_Fig3_HTML.jpg

相似文献

[1]
Exosomal mediators in sepsis and inflammatory organ injury: unraveling the role of exosomes in intercellular crosstalk and organ dysfunction.

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[2]
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[3]
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引用本文的文献

[1]
Identification and Experimental Validation of OS-Related Gene Sets Based on Integrated Analysis of Single-Cell and Bulk RNA Sequencing Data with Machine Learning in Patients with Sepsis.

Inflammation. 2025-8-27

[2]
Alveolar epithelial cells in bacterial sepsis-associated acute lung injury: mechanisms and therapeutic strategies.

Front Immunol. 2025-8-6

[3]
Early use of albumin may increase the risk of sepsis-associated acute kidney injury in sepsis patients: a target trial emulation.

Mil Med Res. 2025-8-21

[4]
Exo-hydrogel therapy: a revolutionary approach to managing diabetic complications.

J Nanobiotechnology. 2025-8-11

[5]
Exosomal miR-218 secreted from endothelial progenitor cells mitigates acute lung injury in sepsis mice by inhibiting HMGA1 in alveolar macrophages.

Stem Cell Res Ther. 2025-8-6

[6]
Research progress on damage-associated molecular patterns in acute kidney injury.

Front Immunol. 2025-7-10

[7]
Nanomaterial-based encapsulation of biochemicals for targeted sepsis therapy.

Mater Today Bio. 2025-7-4

[8]
Crosstalk between lung and extrapulmonary organs in sepsis-related acute lung injury/acute respiratory distress syndrome.

Ann Intensive Care. 2025-7-14

[9]
Immunothrombosis in Sepsis: Cellular Crosstalk, Molecular Triggers, and Therapeutic Opportunities-A Review.

Int J Mol Sci. 2025-6-25

[10]
Exosomes in inflammation and cancer: from bench to bedside applications.

Mol Biomed. 2025-6-10

本文引用的文献

[1]
A mitochondrial NADPH-cholesterol axis regulates extracellular vesicle biogenesis to support hematopoietic stem cell fate.

Cell Stem Cell. 2024-3-7

[2]
Mesenchymal stem cell-derived extracellular vesicles in skin wound healing: roles, opportunities and challenges.

Mil Med Res. 2023-8-17

[3]
Bioengineered exosomal-membrane-camouflaged abiotic nanocarriers: neurodegenerative diseases, tissue engineering and regenerative medicine.

Mil Med Res. 2023-4-27

[4]
The role of extracellular vesicles in cancer.

Cell. 2023-4-13

[5]
Exosome-disrupting peptides for cancer immunotherapy.

Nat Mater. 2023-5

[6]
Immunothrombosis: Molecular Aspects and New Therapeutic Perspectives.

J Clin Med. 2023-2-9

[7]
Extracellular vesicles in the pathogenesis and treatment of acute lung injury.

Mil Med Res. 2022-11-1

[8]
Multifaceted roles of extracellular RNAs in different diseases.

Mil Med Res. 2022-8-11

[9]
MiR-690 treatment causes decreased fibrosis and steatosis and restores specific Kupffer cell functions in NASH.

Cell Metab. 2022-7-5

[10]
Macrophage-derived exosomal aminopeptidase N aggravates sepsis-induced acute lung injury by regulating necroptosis of lung epithelial cell.

Commun Biol. 2022-6-6

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