Kim D W, Langille B L, Wong M K, Gotlieb A I
Department of Pathology, Banting and Best Diabetes Centre, University of Toronto, Toronto General Hospital, Canada.
Circ Res. 1989 Jan;64(1):21-31. doi: 10.1161/01.res.64.1.21.
The available data on F-actin microfilament distribution in vascular endothelial cells in vivo is limited. In this study, the appearance and distribution of endothelial cell microfilaments in the rabbit thoracic aorta, the abdominal aorta and its major arterial branch points, and the aortic bifurcation were examined. Perfusion fixed rabbit aortas were stained in situ for F-actin by infusing rhodamine phalloidin via a peristaltic pump into the aortas at a slow flow rate. This new technique resulted in excellent visualization of branch points and allowed for a precise description of the actin microfilament bundles in endothelial cells along flow dividers. In the thoracic and abdominal aorta, away from branch ostia, actin microfilaments were localized in two regions of the endothelial cells, as a prominent band that completely outlined the cell periphery, and also as short central stress fibers. The central stress fibers were more frequent and prominent in cells of the abdominal aorta. At branch sites and at the aortic bifurcation, long, thick microfilament bundles were present in endothelial cells extending from the tip of the flow divider to a few millimeters along the branch arteries, the aorta, and the iliac arteries. Peripheral actin, however, no longer completely surrounded the cells. The thick bundles were not prominent in endothelial cells located adjacent to the proximal lip of branches or at the iliac arteries opposite the flow divider. This study shows that endothelial cell F-actin microfilament distribution in vivo is well defined along the aortic-arterial system. The prominent central microfilament bundles and the reduced peripheral microfilaments seen at localized regions may reflect an adaptive response to elevated shear stress at these sites.
关于体内血管内皮细胞中F-肌动蛋白微丝分布的现有数据有限。在本研究中,检测了兔胸主动脉、腹主动脉及其主要动脉分支点以及主动脉分叉处内皮细胞微丝的外观和分布。通过蠕动泵以缓慢流速将罗丹明鬼笔环肽注入兔主动脉进行灌注固定,然后对主动脉进行原位F-肌动蛋白染色。这项新技术能够清晰地观察到分支点,并能精确描述沿血流分流器的内皮细胞中的肌动蛋白微丝束。在胸主动脉和腹主动脉中,远离分支开口处,肌动蛋白微丝定位于内皮细胞的两个区域,一个是完全勾勒出细胞周边的明显带,另一个是短的中央应力纤维。中央应力纤维在腹主动脉细胞中更频繁且更明显。在分支部位和主动脉分叉处,从血流分流器尖端沿分支动脉、主动脉和髂动脉延伸数毫米的内皮细胞中存在长而粗的微丝束。然而,周边肌动蛋白不再完全包围细胞。在与分支近端边缘相邻的内皮细胞或与血流分流器相对的髂动脉处的内皮细胞中,粗微丝束并不明显。本研究表明,体内主动脉-动脉系统中内皮细胞F-肌动蛋白微丝分布明确。在局部区域观察到的明显中央微丝束和减少的周边微丝可能反映了这些部位对升高的剪切应力的适应性反应。