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

Mil Med Res

Department of Integrated Traditional Chinese and Western Medicine, West China Hospital of Sichuan University, Chengdu, 610041, China.

Published: November 2022

AI Article Synopsis

  • Acute lung injury (ALI) and acute respiratory distress syndrome (ARDS) are serious conditions marked by severe lung inflammation and high mortality rates, with no effective treatments available despite extensive research.
  • The integrity of the alveolar-capillary barrier and inflammatory responses contribute to lung damage, leading to these conditions.
  • Recent studies highlight the significance of extracellular vesicles (EVs) in cell function and inflammation, suggesting they could be used for diagnosis, and that EVs from mesenchymal stem cells may help reduce inflammation and support lung tissue regeneration.

Article Abstract

Acute lung injury (ALI) and acute respiratory distress syndrome (ARDS) are common life-threatening lung diseases associated with acute and severe inflammation. Both have high mortality rates, and despite decades of research on clinical ALI/ARDS, there are no effective therapeutic strategies. Disruption of alveolar-capillary barrier integrity or activation of inflammatory responses leads to lung inflammation and injury. Recently, studies on the role of extracellular vesicles (EVs) in regulating normal and pathophysiologic cell activities, including inflammation and injury responses, have attracted attention. Injured and dysfunctional cells often secrete EVs into serum or bronchoalveolar lavage fluid with altered cargoes, which can be used to diagnose and predict the development of ALI/ARDS. EVs secreted by mesenchymal stem cells can also attenuate inflammatory reactions associated with cell dysfunction and injury to preserve or restore cell function, and thereby promote cell proliferation and tissue regeneration. This review focuses on the roles of EVs in the pathogenesis of pulmonary inflammation, particularly ALI/ARDS.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9623953PMC
http://dx.doi.org/10.1186/s40779-022-00417-9DOI Listing

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