Exosomes for Intramyocardial Intercellular Communication.
- Cervio E Molecular Cardiology Laboratory, Fondazione Cardiocentro Ticino, Via Tesserete, 6900 Lugano, Switzerland ; Swiss Institute of Regenerative Medicine (SIRM), Taverne, Switzerland.
- Barile L Molecular Cardiology Laboratory, Fondazione Cardiocentro Ticino, Via Tesserete, 6900 Lugano, Switzerland ; Swiss Institute of Regenerative Medicine (SIRM), Taverne, Switzerland.
- Moccetti T Molecular Cardiology Laboratory, Fondazione Cardiocentro Ticino, Via Tesserete, 6900 Lugano, Switzerland ; Swiss Institute of Regenerative Medicine (SIRM), Taverne, Switzerland.
- Vassalli G Molecular Cardiology Laboratory, Fondazione Cardiocentro Ticino, Via Tesserete, 6900 Lugano, Switzerland ; Swiss Institute of Regenerative Medicine (SIRM), Taverne, Switzerland ; Centre Hospitalier Universitaire Vaudois (CHUV), Avenue du Bugnon, 1011 Lausanne, Switzerland.
- 2015-06-20
Published in:
- Stem cells international. - 2015
English
Cross-talk between different cell types plays central roles both in cardiac homeostasis and in adaptive responses of the heart to stress. Cardiomyocytes (CMs) send biological messages to the other cell types present in the heart including endothelial cells (ECs) and fibroblasts. In turn, CMs receive messages from these cells. Recent evidence has now established that exosomes, nanosized secreted extracellular vesicles, are crucial mediators of such messages. CMs, ECs, cardiac fibroblasts, and cardiac progenitor cells (CPCs) release exosomes carrying nonrandom subsets of proteins, lipids, and nucleic acids present in their cells of origin. Exosomes secreted from CMs are internalized by fibroblasts and regulate gene expression in these cells as well as in ECs. CPC-derived exosomes protect CMs against apoptosis while also stimulating angiogenesis. They are rich in cardioprotective and proangiogenic microRNAs such as miR-146, miR-210, and miR-132. When injected into infracted hearts in vivo, CPC-derived exosomes reduce infarct size and improve cardiac function. Thus, exosomes are emerging both as key mediators of intercellular communication in the heart and as therapeutic candidates for heart disease.
- Language
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- English
- Open access status
- gold
- Identifiers
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- DOI 10.1155/2015/482171
- PMID 26089917
- Persistent URL
- https://sonar.ch/global/documents/86148
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