Key result
Cardiac lineage-committed cells show regenerative potential in a murine model of myocardial infarction.
Why the study?
Pluripotent stem cell-derived cardiomyocytes are attractive for cell-based therapy to rescue damaged myocardium, leading to investigation of cardiac lineage-committed cells that retain proliferative capacity.
Do mouse embryonic stem cell-derived PDGFRα+ cardiac lineage committed cells improve cardiac function and histology in a myocardial infarction murine model?
Do mouse embryonic stem cell-derived PDGFRα+ cardiac lineage committed cells improve cardiac function and histology in a myocardial infarction murine model?
Mouse embryonic stem cell-derived PDGFRα+ cardiac lineage committed cells show potential as a cellular resource for cardiac regeneration following myocardial infarction.
BACKGROUND: Pluripotent stem cell-derived cardiomyocytes (CMs) have become one of the most attractive cellular resources for cell-based therapy to rescue damaged cardiac tissue. AIM: cardiac lineage-committed cells (CLCs), which have a proliferative capacity but are in a morphologically and functionally immature state compared with differentiated CMs. METHODS: CMs into a myocardial infarction (MI) murine model and performed functional analysis using transthoracic echocardiography (TTE) and histologic analysis. RESULTS: mural cells. CONCLUSION: CLCs may represent a potential cellular resource for cardiac regeneration.
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Hong et al. (2019) studied Myocardial infarction (murine model). Mouse embryonic stem cell-derived PDGFRα+ cardiac lineage committed cells (CLCs) was evaluated on Functional analysis using transthoracic echocardiography (TTE) and histologic analysis. Cardiac lineage-committed cells (CLCs) may represent a potential cellular resource for cardiac regeneration in a murine model of myocardial infarction.
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