Key result
Intramyocardial unrestricted somatic stem cell injection thickens LV walls and restores LVEF in infarcted rats.
Why the study?
Regenerating the injured heart remains a major challenge, as low cell retention has limited the success of cell therapy for myocardial infarction.
Does intramyocardial injection of USSC improve cardiac regeneration and ejection fraction in infarcted rat hearts?
Does intramyocardial injection of USSC improve cardiac regeneration and ejection fraction in infarcted rat hearts?
Intramyocardial injection of USSC promotes endogenous cardiac regeneration and functional recovery after myocardial infarction through a T-cell-driven paracrine mechanism.
Hypothesis-generating for stem cell-mediated post-MI repair; leaves open translation to human trials.
Regenerating the injured heart remains one of the most vexing challenges in cardiovascular medicine. Cell therapy has shown potential for treatment of myocardial infarction, but low cell retention so far has limited its success. Here we show that intramyocardial injection of highly apoptosis-resistant unrestricted somatic stem cells (USSC) into infarcted rat hearts resulted in an unprecedented thickening of the left ventricular wall with cTnT + /BrdU + cardiomyocytes that was paralleled by progressively restored ejection fraction. USSC induced significant T-cell enrichment in ischemic tissue with enhanced expression of T-cell related cytokines. Inhibition of T-cell activation by anti-CD28 monoclonal antibody, fully abolished the regenerative response which was restored by adoptive T-cell transfer. Secretome analysis of USSC and lineage tracing studies suggest that USSC secrete paracrine factors over an extended period of time which boosts a T-cell driven endogenous regenerative response mainly from adult cardiomyocytes.
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Ding et al. (2022) studied Myocardial infarction. Intramyocardial injection of unrestricted somatic stem cells (USSC) was evaluated on Left ventricular wall thickening and ejection fraction restoration. Intramyocardial injection of unrestricted somatic stem cells into infarcted rat hearts resulted in left ventricular wall thickening and progressively restored ejection fraction.
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