Key result
Serial block-face scanning electron microscopy revealed CD34+/CD44+ vascular-associated cells forming electron-dense contacts with endothelial cells but not pericytes in murine cardiac stroma.
Why the study?
Understanding the spatial cytoarchitecture of the cardiac stroma and myocardial vasculature is essential for developing advanced cardiac tissue engineering and novel therapeutic strategies for heart failure.
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This study provides high-resolution 3D ultrastructural visualizations of the murine cardiac microvasculature, demonstrating direct electron-dense contacts between endothelial cells and CD34+/CD44+ telocyte-like vascular-associated cells that may inform future cardiac tissue engineering strategies.
Cardiac tissue engineering is a promising strategy to restore cardiac function in heart failure patients. Understanding the cardiac tissue architecture including the cardiac stroma is essential for developing not only advanced cardiac tissue engineering but also novel therapeutic strategies. One of the crucial components of the cardiac stroma is the myocardial vasculature. To enhance the spatial visualization of the cardiac stromal cytoarchitecture with a particular focus on myocardial vasculature, we performed 3D reconstructions of the murine cardiac micro vessels using Serial Block-Face Scanning Electron Microscopy (SBF-SEM). These analyses revealed that pericyte cell bodies were primarily oriented lengthwise and extended several cellular protrusions towards the endothelium. At capillary branching points, some pericytes made contact with both capillaries emerging from branching. In addition to pericytes that are completely encapsulated by the common basal lamina together with capillary endothelial cells, we identified other vascular-associated cells located outside this sheath. Based on marker expression, these cells were distinguished from fibroblasts and suggested to be telocytes. The vascular-associated cells formed electron-dense contact zones with endothelial cells, suggesting functional coupling between these both cell types. In conclusion, this study provides detailed three-dimensional visualizations of the cardiac stroma with a particular focus on cardiac microvasculature, offering enhanced insight into the cardiac stromal cytoarchitecture.
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Kleefeldt et al. (2025) studied Normal murine cardiac microvasculature and stroma. 3D reconstruction using Serial Block-Face Scanning Electron Microscopy (SBF-SEM) and immunoelectron microscopy was evaluated on Three-dimensional cytoarchitecture and intercellular interactions of myocardial endothelial cells, pericytes, and vascular-associated cells (VACs). Serial block-face scanning electron microscopy revealed CD34+/CD44+ vascular-associated cells forming electron-dense contacts with endothelial cells but not pericytes in murine cardiac stroma.
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