Dynamic Interstitial Cell Response during Myocardial Infarction Predicts Resilience to Rupture in Genetically Diverse Mice

Cell Rep. 2020 Mar 3;30(9):3149-3163.e6. doi: 10.1016/j.celrep.2020.02.008.

Abstract

Cardiac ischemia leads to the loss of myocardial tissue and the activation of a repair process that culminates in the formation of a scar whose structural characteristics dictate propensity to favorable healing or detrimental cardiac wall rupture. To elucidate the cellular processes underlying scar formation, here we perform unbiased single-cell mRNA sequencing of interstitial cells isolated from infarcted mouse hearts carrying a genetic tracer that labels epicardial-derived cells. Sixteen interstitial cell clusters are revealed, five of which were of epicardial origin. Focusing on stromal cells, we define 11 sub-clusters, including diverse cell states of epicardial- and endocardial-derived fibroblasts. Comparing transcript profiles from post-infarction hearts in C57BL/6J and 129S1/SvImJ inbred mice, which displays a marked divergence in the frequency of cardiac rupture, uncovers an early increase in activated myofibroblasts, enhanced collagen deposition, and persistent acute phase response in 129S1/SvImJ mouse hearts, defining a crucial time window of pathological remodeling that predicts disease outcome.

Keywords: Seurat; cardiac rupture; epicardial-derived; fibrosis; genetic diversity; heart; mouse; myocardial infarction; scRNAseq; single-cell biology.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cicatrix / pathology
  • Homeostasis
  • Mice
  • Mice, Inbred Strains
  • Myocardial Infarction / genetics*
  • Myocardium / pathology*
  • Myofibroblasts / pathology
  • Pericardium / pathology
  • Phenotype
  • RNA-Seq
  • Rupture / pathology*
  • Single-Cell Analysis
  • Stromal Cells / pathology