Schelling M E, Meininger C J, Hawker J R, Granger H J
Department of Medical Physiology, Texas A&M University College of Medicine, College Station 77843.
Am J Physiol. 1988 Jun;254(6 Pt 2):H1211-7. doi: 10.1152/ajpheart.1988.254.6.H1211.
Coronary venular endothelial cells were isolated by a bead-perfusion technique that allowed the selection of endothelial cells from venules of a specific size. Culture conditions for the microvascular cells were established. Cells grew well in supplemented Dulbecco's modified Eagle's medium. The effect of various substrata on the proliferation of the venular endothelial cells was determined. Matrigel, gelatin, and fibronectin supported high levels of proliferation. Cell shape was correlated with ability of the substratum to support cell proliferation. Cells exhibiting a broad, flattened morphology achieved high levels of proliferation. The formation of vessel meshworks by the coronary venular endothelial cells provides an in vitro model for the study of coronary angiogenesis. Confluent monolayers of these cells can be utilized to examine mechanisms of water and protein transport across coronary venules.
采用珠灌注技术分离冠状动脉小静脉内皮细胞,该技术可从特定大小的小静脉中选择内皮细胞。建立了微血管细胞的培养条件。细胞在补充了 Dulbecco 改良 Eagle 培养基中生长良好。测定了各种基质对小静脉内皮细胞增殖的影响。基质胶、明胶和纤连蛋白支持高水平的增殖。细胞形态与基质支持细胞增殖的能力相关。呈现宽扁形态的细胞实现了高水平的增殖。冠状动脉小静脉内皮细胞形成的血管网络为冠状动脉血管生成的研究提供了一个体外模型。这些细胞的汇合单层可用于研究水和蛋白质跨冠状动脉小静脉转运的机制。