Why the study?
Monocytes and macrophages play a critical, dual role in post-ischemic cardiac repair, but how they acquire heterogeneous functional phenotypes in the ischemic myocardium remained unclear.
Population
Mice undergoing experimental MI and homeostatic conditions
Comparison
Post-MI states vs homeostatic conditions
Design
Time-series single-cell transcriptome and cell surface epitope analysis
Follow-up
Up to 11 days after MI
Authors
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Highlights monocyte/macrophage heterogeneity post-MI in mice; leaves open targeted therapies pending human validation.
Single-cell transcriptomic profiling maps the rapid transition of circulating monocytes into distinct, time-dependent macrophage populations (MHCIIhi and Trem2hiIgf1hi) within the ischemic myocardium after myocardial infarction.
Rizzo et al. (2020) studied this question.
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