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Embryonic stem cell and pluripotency proteins (SOX2, OCT4, NANOG, SSEA4, Tra-180, Tra-160) were assessed with immunocytochemistry (Figure 1C)

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812,813,814,815,816,817 HUC-MSCs-derived exosomes directly downregulate the expression of DMT1 through enriched miR-23a-3p, thereby reducing Fe 2+ and MDA levels in cardiomyocytes, inhibiting ferroptosis, and alleviating myocardial injury