Intra-cardiac release of extracellular vesicles shapes inflammation following myocardial infarction short communication

Xavier Loyer, Ivana Zlatanova, Cecile Devue, Min Yin, Kiave Yune Howangyin, Phatchanat Klaihmon, Coralie L. Guerin, Marouane Khelouf, Jose Vilar, Konstantinos Zannis, Bernd K. Fleischmann, Do Won Hwang, Jongmin Park, Hakho Lee, Philippe Menasché, Jean Sébastien Silvestre, Chantal M. Boulanger*

*Corresponding author for this work

Research output: Contribution to journalArticleResearchpeer-review

149 Citations (Scopus)


Rationale: A rapid and massive influx of inflammatory cells occurs into ischemic area after myocardial infarction (MI), resulting in local release of cytokines and growth factors. Yet, the mechanisms regulating their production are not fully explored. The release of extracellular vesicles (EVs) in the interstitial space curbs important biological functions, including inflammation, and influences the development of cardiovascular diseases. To date, there is no evidence for in situ release of cardiac EVs after MI. Objective: The present study tested the hypothesis that local EV generation in the infarcted heart coordinates cardiac inflammation after MI. Methods and Results: Coronary artery ligation in mice transiently increases EV levels in the left ventricle when compared with sham animals. EVs from infarcted hearts were characterized as large vesicles (252±18 nm) expressing cardiomyocyte and endothelial markers and small EVs (118±4 nm) harboring exosomal markers, such as CD (cluster of differentiation) 63 and CD9. Cardiac large EVs generated after MI, but not small EVs or sham EVs, increased the release of IL (interleukin)-6, CCL (chemokine ligand) 2, and CCL7 from fluorescence-activated cell-sorted Ly6C+ cardiac monocytes. EVs of similar diameter were also isolated from fragments of interventricular septum obtained from patients undergoing aortic valve replacement, thus supporting the clinical relevance of our fndings in mice. Conclusions: The present study demonstrates that acute MI transiently increases the generation of cardiac EVs characterized as both exosomes and microvesicles, originating mainly from cardiomyocytes and endothelial cells. EVs accumulating in the ischemic myocardium are rapidly taken up by infltrating monocytes and regulate local inflammatory responses.

Original languageEnglish
Pages (from-to)100-106
Number of pages7
JournalCirculation Research
Issue number1
Publication statusPublished - 2018


  • Exosomes
  • Humans
  • Inflammation
  • Myocardial infarction
  • Myocytes
  • cardiac


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