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Targeting Inflammation after Myocardial Infarction: A Therapeutic Opportunity for Extracellular Vesicles?

Title: Targeting Inflammation after Myocardial Infarction: A Therapeutic Opportunity for Extracellular Vesicles?
Authors: Margarida Viola; Saskia C. A. de Jager; Joost P. G. Sluijter
Source: International Journal of Molecular Sciences, Vol 22, Iss 7831, p 7831 (2021)
Publisher Information: MDPI AG
Publication Year: 2021
Collection: Directory of Open Access Journals: DOAJ Articles
Subject Terms: myocardial infarction; cardiac inflammation; monocyte influx; macrophage polarization; immunomodulatory therapy; extracellular vesicles; Biology (General); QH301-705.5; Chemistry; QD1-999
Description: After myocardial infarction (MI), a strong inflammatory response takes place in the heart to remove the dead tissue resulting from ischemic injury. A growing body of evidence suggests that timely resolution of this inflammatory process may aid in the prevention of adverse cardiac remodeling and heart failure post-MI. The present challenge is to find a way to stimulate this process without interfering with the reparative role of the immune system. Extracellular vesicles (EVs) are natural membrane particles that are released by cells and carry different macromolecules, including proteins and non-coding RNAs. In recent years, EVs derived from various stem and progenitor cells have been demonstrated to possess regenerative properties. They can provide cardioprotection via several mechanisms of action, including immunomodulation. In this review, we summarize the role of the innate immune system in post-MI healing. We then discuss the mechanisms by which EVs modulate cardiac inflammation in preclinical models of myocardial injury through regulation of monocyte influx and macrophage function. Finally, we provide suggestions for further optimization of EV-based therapy to improve its potential for the treatment of MI.
Document Type: article in journal/newspaper
Language: English
Relation: https://www.mdpi.com/1422-0067/22/15/7831; https://doaj.org/toc/1661-6596; https://doaj.org/toc/1422-0067; https://doaj.org/article/dce2ddef735a492381012fad0535363d
DOI: 10.3390/ijms22157831
Availability: https://doi.org/10.3390/ijms22157831; https://doaj.org/article/dce2ddef735a492381012fad0535363d
Accession Number: edsbas.DDBB7E06
Database: BASE