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细胞外囊泡:脓毒症和急性呼吸窘迫综合征的新角色。

Extracellular Vesicles, New Players in Sepsis and Acute Respiratory Distress Syndrome.

机构信息

Department of Critical Care Medicine, Renmin Hospital of Wuhan University, Hubei Key Laboratory of Cell Homeostasis, College of Life Sciences, Wuhan University, Wuhan, China.

Department of Critical Care Medicine, Renmin Hospital of Wuhan University, Wuhan, China.

出版信息

Front Cell Infect Microbiol. 2022 Apr 7;12:853840. doi: 10.3389/fcimb.2022.853840. eCollection 2022.


DOI:10.3389/fcimb.2022.853840
PMID:35463634
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9021632/
Abstract

Sepsis refers to a complex syndrome associated with physiological, pathological, and biochemical abnormalities resulted from infection. Sepsis is the major cause of acute respiratory distress syndrome (ARDS). Extracellular vesicles (EVs) are serving as new messengers to mediate cell-cell communication . Non-coding RNAs, proteins and metabolites encapsulated by EVs could result in either pro-inflammatory or anti-inflammatory effects in the recipient cells. Pathogens or host cells derived EVs play an important role in pathogens infection during the occurrence and development of sepsis and ARDS. Additionally, we summarize the potential application for EVs in diagnosis, prevention and treatment for sepsis and ARDS.

摘要

脓毒症是一种与感染引起的生理、病理和生化异常相关的复杂综合征。脓毒症是急性呼吸窘迫综合征(ARDS)的主要病因。细胞外囊泡(EVs)作为新的信使,介导细胞间通讯。EVs 包裹的非编码 RNA、蛋白质和代谢物可在受体细胞中产生促炎或抗炎作用。病原体或宿主细胞衍生的 EVs 在脓毒症和 ARDS 的发生和发展过程中病原体感染中发挥重要作用。此外,我们总结了 EVs 在脓毒症和 ARDS 的诊断、预防和治疗中的潜在应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b233/9021632/19be2a0565e2/fcimb-12-853840-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b233/9021632/8acd201bc9f0/fcimb-12-853840-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b233/9021632/19be2a0565e2/fcimb-12-853840-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b233/9021632/8acd201bc9f0/fcimb-12-853840-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b233/9021632/19be2a0565e2/fcimb-12-853840-g002.jpg

相似文献

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Extracellular Vesicles, New Players in Sepsis and Acute Respiratory Distress Syndrome.

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[2]
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[9]
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[10]
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引用本文的文献

[1]
Adipose-derived mesenchymal stem cell-derived extracellular vesicles carry microRNA-214-3p to target GSTZ1 to curb ferroptosis in lung epithelial cells during sepsis.

Cytotechnology. 2025-8

[2]
Antibiotic treatment modulates -derived bacterial extracellular vesicle (BEV) production and their capacity to upregulate ICAM-1 in human endothelial cells.

bioRxiv. 2025-5-13

[3]
Predicting mortality and risk factors of sepsis related ARDS using machine learning models.

Sci Rep. 2025-4-18

[4]
Global trends in research on endothelial cells and sepsis between 2002 and 2022: A systematic bibliometric analysis.

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[5]
Regulation of Extracellular Vesicle-Mediated Immune Responses against Antigen-Specific Presentation.

Vaccines (Basel). 2022-10-10

本文引用的文献

[1]
Calming egress of inflammatory monocytes and related septic shock by therapeutic CCR2 silencing using macrophage-derived extracellular vesicles.

Nanoscale. 2022-3-31

[2]
Mechanism and Potential of Extracellular Vesicles Derived From Mesenchymal Stem Cells for the Treatment of Infectious Diseases.

Front Microbiol. 2021-10-26

[3]
Functional delivery of lncRNA TUG1 by endothelial progenitor cells derived extracellular vesicles confers anti-inflammatory macrophage polarization in sepsis via impairing miR-9-5p-targeted SIRT1 inhibition.

Cell Death Dis. 2021-11-6

[4]
Extracellular Vesicle-Based Therapy for COVID-19: Promises, Challenges and Future Prospects.

Biomedicines. 2021-10-1

[5]
Long Non-Coding RNAs as Biomarkers and Therapeutic Targets in Sepsis.

Front Immunol. 2021

[6]
Extracellular vesicles in acute respiratory distress syndrome: Recent developments from bench to bedside.

Int Immunopharmacol. 2021-11

[7]
Extracellular Vesicles: A Double-Edged Sword in Sepsis.

Pharmaceuticals (Basel). 2021-8-23

[8]
Therapeutic Potential of Extracellular Vesicles for Sepsis Treatment.

Adv Ther (Weinh). 2021-7

[9]
Combined glucocorticoid resistance and hyperlactatemia contributes to lethal shock in sepsis.

Cell Metab. 2021-9-7

[10]
Acute respiratory distress syndrome.

Lancet. 2021-8-14

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