Extracellular vesicles derived from anoxia-preconditioned adipose-derived mesenchymal stem cells significantly reduced infarct size and cardiomyocyte apoptosis compared to normoxic EVs in a mouse model of myocardial ischemia-reperfusion injury.
Do anoxia-preconditioned ADSC EVs reduce infarct size and cardiomyocyte apoptosis in mice with myocardial ischemia/reperfusion injury compared to normoxic ADSC EVs?
Anoxia-preconditioned mesenchymal stem cell-derived extracellular vesicles protect against myocardial ischemia/reperfusion injury by delivering miRNA224-5p, which downregulates TXNIP and prevents cardiomyocyte apoptosis.
p-value: p=0.0028
. Injection of anoxia-preconditioned ADSC EVs (Int-EVs) reduced both infarct size and cardiomyocyte apoptosis to a greater extent than normoxic ADSC EVs (NC-EVs) in mice subjected to MIRI. Sequencing EV-associated miRNAs revealed differential upregulation of ten miRNAs predicted to bind thioredoxin-interacting protein (TXNIP), an inflammasome- and pyroptosis-related protein. We confirmed direct binding of miRNA224-5p, the most upregulated miRNA in Int-EVs, to TXNIP and asserted through western blotting and apoptosis assays a critical protective role for this miRNA against AR-induced cardiomyocyte death. Our results suggest that ischemia-reperfusion triggers TXNIP-induced inflammasome activation in cardiomyocytes, which leads to apoptosis rather than pyroptosis due to low basal levels of the pyroptosis executioner protein gasdermin D in these cells. The antiapoptotic effect of EV-associated miRNA224-5p would in turn result from TXNIP downregulation, which prevents caspase-1-mediated degradation of GATA4 and sustains the expression of Bcl-2.
Mao et al. (Fri,) conducted a other in Myocardial ischemia-reperfusion injury (MIRI) (n=80). Extracellular vesicles from anoxia-preconditioned adipose-derived mesenchymal stem cells (Int-EVs) vs. Extracellular vesicles from normoxic ADSCs (NC-EVs) or Ischemia-reperfusion alone was evaluated on Infarct size (p=0.0028). Extracellular vesicles derived from anoxia-preconditioned adipose-derived mesenchymal stem cells significantly reduced infarct size and cardiomyocyte apoptosis compared to normoxic EVs in a mouse model of myocardial ischemia-reperfusion injury.