Relou I A, Damen C A, van der Schaft D W, Groenewegen G, Griffioen A W
Department of Internal Medicine and Medical Oncology, University Hospital Utrecht, GA Utrecht, The Netherlands.
Tissue Cell. 1998 Oct;30(5):525-30. doi: 10.1016/s0040-8166(98)80032-3.
The in vitro culture of endothelial cells (EC) is dependent on the presence of a coated surface and the availability of growth factors in the medium. The aim of the present research is to investigate whether in vitro EC culture conditions, such as serum source and surface coating, determine the growth characteristics of EC. The phenotype of EC was studied at the level of adhesion molecule expression and down-regulation by angiogenic factors. We found that human umbilical vein EC adhere well to and stretch well with plastic coated with fibronectin, collagen, gelatin and hyaluronan in contrast to non-coated plastic. While low in hyaluronan-coated wells, the spontaneous proliferation of EC was enhanced in fibronectin-collagen and gelatin-coated wells as compared to non-coated wells. Basic fibroblast growth factor bFGF-induced proliferation, however, was best on hyaluronan-coated plastic. A markedly up-regulated proliferation was measured on fibronectin and collagen while EC on gelatin-coated plastic only showed moderate bFGF-induced proliferation. On non-coated plastic EC were not inducible with bFGF. The induction of apoptosis by serum deprivation on these different matrices was most efficient when no coat was available or when wells were coated with hyaluronan, and bFGF inhibited apoptosis induction under all conditions. The use of different culture media demonstrated that human and bovine serum both can be used for human EC assays. The synthetic medium Utroser G prevented both spontaneous and growth factor-induced proliferation. We found that apart from some magnitude differences, the down-regulation of intercellular adhesion molecule-1 (ICAM-1) by angiogenic factors such as bFGF is not dependent on specific culture conditions.
内皮细胞(EC)的体外培养依赖于包被表面的存在以及培养基中生长因子的可用性。本研究的目的是调查体外EC培养条件,如血清来源和表面包被,是否决定EC的生长特性。在粘附分子表达水平以及血管生成因子对其下调方面研究了EC的表型。我们发现,与未包被的塑料相比,人脐静脉EC在包被有纤连蛋白、胶原蛋白、明胶和透明质酸的塑料上粘附良好且伸展良好。虽然在透明质酸包被的孔中较低,但与未包被的孔相比,在纤连蛋白-胶原蛋白和明胶包被的孔中EC的自发增殖增强。然而,碱性成纤维细胞生长因子bFGF诱导的增殖在透明质酸包被的塑料上最佳。在纤连蛋白和胶原蛋白上测得增殖明显上调,而在明胶包被的塑料上的EC仅显示适度的bFGF诱导增殖。在未包被的塑料上,EC不能被bFGF诱导。当没有包被或孔被透明质酸包被时,血清剥夺在这些不同基质上诱导凋亡最有效,并且bFGF在所有条件下均抑制凋亡诱导。使用不同的培养基表明,人血清和牛血清均可用于人EC检测。合成培养基Utroser G可防止自发增殖和生长因子诱导的增殖。我们发现,除了一些程度上的差异外,血管生成因子如bFGF对细胞间粘附分子-1(ICAM-1)的下调不依赖于特定的培养条件。