Key result
Stem cell-derived exosomes show promise for cardiac repair and reducing inflammation after myocardial infarction.
Why the study?
Despite promising results from stem cell therapy in cardiac repair, the underlying mechanisms of their functional efficacy remain controversial, particularly regarding their ability to adopt cardiac phenotypes versus paracrine effects.
This review highlights the paracrine hypothesis as a primary mechanism by which stem cell therapy may confer beneficial effects in cardiac repair following myocardial infarction.
Hypothesis-generating for post-MI repair; leaves open clinical translation pending randomized trials.
Last two decades of research has seen the emergence and progress of stem cells from a myth to reality and their expediency in the clinical perspective as an effective therapeutic modality. Despite immense progress and promising results from experimental animal studies and clinical trials, the provocative underlying mechanism of their functional efficacy has led to diverging opinions and indulging the researchers into a continuous discussion. With controversies clouding the potential of stem cells to adopt morpho functionally competent cardiac phenotype, paracrine activity of the transplanted stem cells has been put forth as an alternative mechanism associated with the beneficial outcome of cell therapy. Although unique paracrine activity of a cell, besides endocrine activity and juxtacrine activity, constitutes an integral part of the cell-to-cell communication, the release of trophic factors from the transplanted cells favorably modulates the local microenvironment in the cell transplanted region in the infarcted heart and positively impact the integration and reparability of the cell graft.
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KH et al. (2017) conducted an editorial in Myocardial infarction. Stem cell-derived conditioned medium and exosomes was evaluated.
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