Anoctamin 1 Positive Esophageal Interstitial Cajal Cells in Late Stage Human Embryos

• Published in: Anatomical record (Hoboken, N.J. : 2007) N.J. : 2007), 2014-02, Vol.297 (2), p.301-307
• Main Authors: Rusu, Mugurel Constantin, Poalelungi, Cristian Viorel, Vrapciu, Alexandra Diana, Păduraru, Luminiţa, Didilescu, Andreea Cristiana, Stan, Cristinel Ionel
• Format: Article
• Language: English
• Subjects: Actins - metabolism; Anoctamin-1; Antigens, CD34 - metabolism; CD31; CD34; Chloride Channels - metabolism; Desmin - metabolism; DOG1; embryology; endothelial tip cells; Esophagus - cytology; Esophagus - embryology; Esophagus - metabolism; Humans; Interstitial Cells of Cajal - cytology; Interstitial Cells of Cajal - metabolism; Morphogenesis - physiology; Muscle, Smooth - cytology; Muscle, Smooth - embryology; Muscle, Smooth - metabolism; Neoplasm Proteins - metabolism; nestin; Nestin - metabolism; Platelet Endothelial Cell Adhesion Molecule-1 - metabolism; smooth muscle actin
• ISSN: 1932-8486; 1932-8494
• DOI: 10.1002/ar.22837

ABSTRACT Interstitial cells of Cajal (ICCs) are located in various smooth muscle organs and act as pacemaker cells, or ensure neuromodulation or mechanosensory roles. The study aims to investigate functional states of human ICCs in morphogenesis, focusing on the anoctamin 1 phenotype. The investigation was performed in five late stage human embryos with lengths varying between 23 and 29 mm. Immunohistochemistry on paraffin embedded specimens was performed for a series of antibodies: α‐smooth muscle actin (α‐SMA), desmin, CD31, CD34, CD117/c‐kit, DOG1, and nestin. Longitudinal and circular muscle layers were α‐SMA+/desmin+/nestin+. An immature microvascular layer located in the inner submucosa was CD34+/CD31+/α‐SMA+/nestin+; endothelial tip cells were supporting active processes of sprouting angiogenesis. A CD34+/CD31‐ mesenchymal network was found in the circular muscle layer. CD117/c‐kit+ multipolar ICCs with dichotomizing processes were found mostly in the myenteric plexus layer; processes were configuring a network within the circular muscle layer where intramuscular ICCs were scarcely found. A strong DOG1+ reaction was found for the ICCs of the myenteric plexus layer apposed on the outer surface of the circular muscle layer, and for the intramuscular ICCs. The evidence of a sublayer of DOG1+ myenteric ICCs is suggestive for a subpopulation of ICCs being qualified for pacemaking at this early developmental stage. Anat Rec, 297:301–307, 2014. © 2013 Wiley Periodicals, Inc.