3-D reconstruction and multiple marker analysis of mouse proepicardial endothelial cell population

Microvasc Res. 2015 Nov:102:54-69. doi: 10.1016/j.mvr.2015.08.007. Epub 2015 Aug 12.

Abstract

Background: The proepicardium (PE), a transient embryonic structure crucial for the development of the epicardium and heart, contains its own population of endothelial cells (ECs). The aim of our study was to determine the pattern, anatomical orientation and phenotypic marker expression of the endothelial cell network within the PE.

Results: Immunohistochemical findings revealed that proepicardial ECs express both early and late EC-specific markers such as CD31, Flk-1, Lyve-1 and Tie-2 but not SCL/Tal1, vWF, Dll4 or Notch1. Proepicardial ECs are present in the vicinity of the sinus venosus (SV) and form a continuous network of vascular sprouts/tubules connected with the SV endothelium, with Ter-119-positive erythroblasts in the vascular lumina.

Conclusions: On the basis of our results, we postulate the existence of a continuous network of ECs in the PE, exhibiting connection and/or patency with the SV and forming vessels/tubules/strands. Marker expression suggests that ECs are immature and undifferentiated, which was also confirmed with a transmission electron microscopy (TEM) analysis. Our results deliver new data for a better understanding of the nature of proepicardial ECs.

Keywords: CD31; Liver bud; Lyve-1; Proepicardium; Prox1; Ter-119.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Biomarkers / metabolism
  • Cell Differentiation
  • Endothelial Cells / cytology*
  • Endothelial Cells / metabolism*
  • Female
  • Gestational Age
  • Glycoproteins / metabolism
  • Imaging, Three-Dimensional
  • Immunohistochemistry
  • Male
  • Membrane Transport Proteins
  • Mice
  • Mice, Inbred C57BL
  • Mice, Inbred CBA
  • Microscopy, Electron, Transmission
  • Models, Cardiovascular
  • Pericardium / embryology*
  • Pericardium / metabolism*
  • Platelet Endothelial Cell Adhesion Molecule-1 / metabolism
  • Pregnancy
  • Receptor, TIE-2 / metabolism
  • Vascular Endothelial Growth Factor Receptor-2 / metabolism

Substances

  • Biomarkers
  • Glycoproteins
  • Membrane Transport Proteins
  • Platelet Endothelial Cell Adhesion Molecule-1
  • Xlkd1 protein, mouse
  • Receptor, TIE-2
  • Tek protein, mouse
  • Vascular Endothelial Growth Factor Receptor-2