关键词: Cardiac stem cells Immunohistochemistry Myocardium Pericytes Stem niches

Mesh : Actins / analysis Animals Antigens, CD34 / analysis Humans Immunohistochemistry Myocardium / cytology ultrastructure Pericytes / cytology ultrastructure Platelet Endothelial Cell Adhesion Molecule-1 / analysis Proto-Oncogene Proteins c-kit / analysis Receptor, Platelet-Derived Growth Factor alpha / analysis Stem Cells / cytology Telocytes / cytology ultrastructure

来  源:   DOI:10.1159/000497194   PDF(Sci-hub)

Abstract:
Telocytes (TCs) are a controversial cell type characterized by the presence of a particular kind of prolongations, known as telopodes, which are long, thin, and moniliform. A number of attempts has been made to establish the molecular phenotype of cardiac TCs (i.e., expression of c-kit, CD34, vimentin, PDGRFα, PDGRFβ, etc.). We designed an immunohistochemical study involving cardiac tissue samples obtained from 10 cadavers with the aim of determining whether there are TC-like interstitial cells that populate the interstitial space other than the mural microvascular cells. We applied the markers for CD31, CD34, PDGRFα, CD117/c-kit, and α-smooth muscle actin (α-SMA). We found that, in relation to two-dimensional cuts, the endothelial tubes could be misidentified as TC-like cells, the difference being the positive identification of endothelial lumina. Moreover, we found that cardiac pericytes express PDGRFα, CD117/c-kit, and α-SMA, and that they could also be misidentified as TCs when using light microscopy. We reviewed the respective values of the previously identified markers for achieving a clear-cut identification of cardiac TCs, highlighting the critical lack of specificity.
摘要:
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