Dobrina A, Soranzo M R, Rossi F
Cell Tissue Res. 1983;232(3):579-91. doi: 10.1007/BF00216430.
Work on endothelial cells has been limited by the availability of procedures for obtaining such cells in quantities adequate for direct in vitro analysis. The present paper describes a method for the isolation of endothelial cells from bovine cavernous bodies. A number of cells ranging from 2.5 to 4 X 10(8) per animal has been obtained. The cells were identified as follows 1) presence of the "Weibel and Palade" bodies in the isolated cells, 2) "cobblestone" appearance of cell cultures, and 3) presence of factor VIII, as demonstrated by immunofluorescence assays. The cell viability at the end of the purification procedure was tested 1) by dye-exclusion tests and 2) by metabolic assays. Features of this preparation are 1) the very high yield of viable endothelial cells, 2) the absence of contamination by fibroblasts and smooth muscle cells and a very low contamination by erythrocytes and 3) the fine dispersion of the isolated cells. These properties allow functional and subcellular fractionation studies on freshly isolated endothelial cells of microvascular origin.
对内皮细胞的研究一直受到获取足够数量细胞以进行直接体外分析的方法的限制。本文描述了一种从牛海绵体中分离内皮细胞的方法。每只动物已获得2.5至4×10⁸个细胞。这些细胞通过以下方式进行鉴定:1)分离细胞中存在“魏贝尔-帕拉德小体”;2)细胞培养呈现“鹅卵石”外观;3)免疫荧光测定显示存在凝血因子VIII。在纯化过程结束时,通过以下两种方法测试细胞活力:1)染料排除试验;2)代谢测定。该制备方法的特点包括:1)活内皮细胞产量极高;2)无成纤维细胞和平滑肌细胞污染,红细胞污染极低;3)分离细胞分散良好。这些特性使得能够对微血管来源的新鲜分离内皮细胞进行功能和亚细胞分级研究。