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Prevention of atrial fibrillation after open-chest surgery with extracellular vesicle therapy
Sandrine Parent, Ramana Vaka, Yousef Risha, Clarissa Ngo, Pushpinder Kanda, Stanley Nattel, Saad Khan, David Courtman, Duncan J. Stewart, Darryl R. Davis
Sandrine Parent, Ramana Vaka, Yousef Risha, Clarissa Ngo, Pushpinder Kanda, Stanley Nattel, Saad Khan, David Courtman, Duncan J. Stewart, Darryl R. Davis
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Research Article Cardiology

Prevention of atrial fibrillation after open-chest surgery with extracellular vesicle therapy

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Abstract

Almost half of patients recovering from open-chest surgery experience atrial fibrillation (AF) that results principally from inflammation in the pericardial space surrounding the heart. Given that postoperative AF is associated with increased mortality, effective measures to prevent AF after open-chest surgery are highly desirable. In this study, we tested the concept that extracellular vesicles (EVs) isolated from human atrial explant-derived cells can prevent postoperative AF. Middle-aged female and male rats were randomized to undergo sham operation or induction of sterile pericarditis followed by trans-epicardial injection of human EVs or vehicle into the atrial tissue. Pericarditis increased the probability of inducing AF while EV treatment abrogated this effect in a sex-independent manner. EV treatment reduced infiltration of inflammatory cells and production of pro-inflammatory cytokines. Atrial fibrosis and hypertrophy seen after pericarditis were markedly attenuated by EV pretreatment, an effect attributable to suppression of fibroblast proliferation by EVs. Our study demonstrates that injection of EVs at the time of open-chest surgery shows prominent antiinflammatory effects and prevents AF due to sterile pericarditis. Translation of this finding to patients might provide an effective new strategy to prevent postoperative AF by reducing atrial inflammation and fibrosis.

Authors

Sandrine Parent, Ramana Vaka, Yousef Risha, Clarissa Ngo, Pushpinder Kanda, Stanley Nattel, Saad Khan, David Courtman, Duncan J. Stewart, Darryl R. Davis

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Figure 1

Characterization of extracellular vesicles produced by human atrial explant-derived cells cultured under serum-free, xenogen-free culture conditions within a clinical cell manufacturing facility.

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Characterization of extracellular vesicles produced by human atrial expl...
(A) Proteomic array demonstrating presence of markers indicative of EV identity while lacking cellular contaminants. (B) Flow cytometry demonstrating the relationship between EV size and surface marker expression (n = 3 biological replicates). One-way ANOVA with individual-mean comparisons by Bonferroni’s multiple 2-tailed comparisons test. (C) Simple linear regression of the relationship between EV concentration and acetylcholinesterase activity (n = 5 biological replicates). Data are plotted showing the 95% confidence bands of the best fit line. (D) Relative abundance of microRNA transcripts within EDC EVs (n = 3 biological replicates). EV, extracellular vesicles; FDR, false discovery rate; miR, microRNA.

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