Skip to Content
Merck

Endocardium Contributes to Cardiac Fat.

Circulation research (2015-12-15)
Hui Zhang, Wenjuan Pu, Qiaozhen Liu, Lingjuan He, Xiuzhen Huang, Xueying Tian, Libo Zhang, Yu Nie, Shengshou Hu, Kathy O Lui, Bin Zhou
ABSTRACT

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. To trace the developmental origin of intramyocardial adipocytes. 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. 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.

MATERIALS
Product Number
Brand
Product Description

Sigma-Aldrich
Anti-Perilipin A antibody produced in rabbit, affinity isolated antibody, buffered aqueous solution