Unger Ronald E, Krump-Konvalinkova Vera, Peters Kirsten, Kirkpatrick C James
Institute of Pathology, Johannes Gutenberg University, Langenbeckstrasse 1, D-55101 Mainz, Germany.
Microvasc Res. 2002 Nov;64(3):384-97. doi: 10.1006/mvre.2002.2434.
Endothelial cell lines are commonly used in in vitro studies to avoid problems associated with the use of primary endothelial cells such as the presence of contaminating cells, the difficulty in obtaining larger numbers of cells, as well as the progressive loss of cell viability and expression of endothelial markers in the course of in vitro propagation. We have analyzed the characteristics defining distinctive endothelial phenotypes in the cell lines EA.hy926, ECV304, EVLC2, HAEND, HMEC-1, ISO-HAS-1 and a cell line recently generated in our laboratory, HPMEC-ST1.6R, and have compared these phenotypes with those found in primary human endothelial cells isolated from umbilical vein (HUVEC), lung (HPMEC), and skin (HDMEC). The analysis revealed significant differences in phenotype expression between primary cells and the cell lines. Constitutive expression of von Willebrand factor, CD31, and CD34 and induced expression of cell adhesion molecules, ICAM-1, VCAM-1, and E-selectin and cytokines, IL-6, IL-8, MCP-1, and GM-CSF on stimulation with proinflammatory stimuli, as well as the uptake of DiI-Ac-LDL and the formation of cord-like structures on Matrigel, were typically observed in the primary cells. However, most cell lines exhibited only a few of these endothelial characteristics. Only HPMEC-ST1.6R exhibited the major constitutive and inducible endothelial cell characteristics and showed an angiogenic response on Matrigel similar to that of primary HPMEC. Thus, HPMEC-ST1.6R will be a valuable in vitro model system in which to study pathomechanisms and angiogenesis of the mature microvascular endothelium in vitro.
内皮细胞系常用于体外研究,以避免使用原代内皮细胞时出现的问题,如存在污染细胞、难以获得大量细胞,以及在体外传代过程中细胞活力和内皮标志物表达的逐渐丧失。我们分析了EA.hy926、ECV304、EVLC2、HAEND、HMEC-1、ISO-HAS-1等细胞系以及我们实验室最近构建的细胞系HPMEC-ST1.6R中定义独特内皮表型的特征,并将这些表型与从人脐静脉(HUVEC)、肺(HPMEC)和皮肤(HDMEC)分离的原代人内皮细胞中的表型进行了比较。分析揭示了原代细胞和细胞系之间在表型表达上的显著差异。原代细胞通常观察到血管性血友病因子、CD31和CD34的组成性表达,以及在促炎刺激下细胞黏附分子ICAM-1、VCAM-1和E-选择素以及细胞因子IL-6、IL-8、MCP-1和GM-CSF的诱导表达,还有DiI-Ac-LDL的摄取以及在基质胶上形成索状结构。然而,大多数细胞系仅表现出这些内皮特征中的少数几种。只有HPMEC-ST1.6R表现出主要的组成性和诱导性内皮细胞特征,并在基质胶上显示出与原代HPMEC相似的血管生成反应。因此,HPMEC-ST1.6R将是一种有价值的体外模型系统,可用于在体外研究成熟微血管内皮的病理机制和血管生成。