Endocardium Contributes to Cardiac Fat

Circ Res. 2016 Jan 22;118(2):254-65. doi: 10.1161/CIRCRESAHA.115.307202. Epub 2015 Dec 9.

Abstract

Rationale: Unraveling the developmental origin of cardiac fat could offer important implications for the treatment of cardiovascular disease. The recent identification of the mesothelial source of epicardial fat tissues reveals a heterogeneous origin of adipocytes in the adult heart. However, the developmental origin of adipocytes inside the heart, namely intramyocardial adipocytes, remains largely unknown.

Objective: To trace the developmental origin of intramyocardial adipocytes.

Methods and results: In this study, we identified that the majority of intramyocardial adipocytes were restricted to myocardial regions in close proximity to the endocardium. Using a genetic lineage tracing model of endocardial cells, we found that Nfatc1(+) endocardial cells contributed to a substantial number of intramyocardial adipocytes. Despite the capability of the endocardium to generate coronary vascular endothelial cells surrounding the intramyocardial adipocytes, results from our lineage tracing analyses showed that intramyocardial adipocytes were not derived from coronary vessels. Nevertheless, the endocardium of the postnatal heart did not contribute to intramyocardial adipocytes during homeostasis or after myocardial infarction.

Conclusions: Our in vivo fate-mapping studies demonstrated that the developing endocardium, but not the vascular endothelial cells, gives rise to intramyocardial adipocytes in the adult heart.

Keywords: adipocytes; endocardium; endothelial cells; homeostasis; pericardium.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adipocytes / cytology*
  • Adipocytes / metabolism
  • Adipogenesis*
  • Animals
  • Biomarkers / metabolism
  • Cell Lineage*
  • Disease Models, Animal
  • Endocardium / cytology*
  • Endocardium / metabolism
  • Fetal Heart / cytology*
  • Gene Expression Regulation, Developmental
  • Gestational Age
  • Homeostasis
  • Mice, Inbred C57BL
  • Mice, Inbred ICR
  • Mice, Transgenic
  • Myocardial Infarction / metabolism
  • Myocardial Infarction / pathology
  • NFATC Transcription Factors / genetics
  • NFATC Transcription Factors / metabolism
  • Phenotype

Substances

  • Biomarkers
  • NFATC Transcription Factors
  • Nfatc1 protein, mouse