Vascular Biology |
From the Second Department of Pathology (E.S., M.S., H.M.), Akita University School of Medicine, Akita, Japan, and the Department of Surgery (E.S., M.S., T.M.S., C.X., C.K.Z.), Stanford University School of Medicine, Stanford, Calif.
Correspondence to Eiketsu Sho, MD, PhD, Division of Vascular Surgery, Stanford University School of Medicine, Stanford, CA 94305-5642. E-mail jsho{at}stanford.edu
AbstractWe investigated apoptosis of endothelial cells during the arterial narrowing process in response to reduction in flow. The decrease in flow was created in the carotid artery by closure of an arteriovenous fistula (AVF), which had been established for 28 days in rabbits. The endothelial cell apoptosis in the carotid artery was studied at 1, 3, 7, and 21 days of flow reduction after closure of the AVF by use of terminal deoxynucleotidyl transferasemediated dUTP nick end-labeling (TUNEL) with laser scanning confocal microscopy and transmission and scanning electron microscopy. After AVF closure, arterial lumen diameter was reduced by 36%, and compared with endothelial cells before the closure, the number of endothelial cells was decreased by 45% at 21 days. Endothelial cell apoptosis was observed at 1 day, peaked at 3 days (381.3±87.1 cells per square millimeter), and decreased at 7 days. These cells had irregular protrusions under scanning electron microscopy and were characterized by fragmented nuclei under transmission electron microscopy. Apoptotic cells were mainly beneath the endothelium and were occasionally within smooth muscle cells and endothelial cells. The results suggest that apoptosis of endothelial cells may play a role in the arterial remodeling in response to a reduction in flow.
Key Words: blood flow wall shear stress endothelial cells apoptosis arterial remodeling
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