Lazarovici Philip, Lahiani Adi, Gincberg Galit, Haham Dikla, Fluksman Arnon, Benny Ofra, Marcinkiewicz Cezary, Lelkes Peter I
Faculty of Medicine, School of Pharmacy, Institute for Drug Research, The Hebrew University of Jerusalem, Jerusalem, Israel.
Department of Bioengineering, College of Engineering, Temple University, Philadelphia, PA, USA.
Methods Mol Biol. 2018;1727:239-250. doi: 10.1007/978-1-4939-7571-6_18.
Nerve growth factor (NGF) is a neurotrophin promoting survival, proliferation, differentiation, and neuroprotection in the embryonal and adult nervous system. NGF also induces angiogenic effects in the cardiovascular system, which may be beneficial in engineering new blood vessels and for developing novel anti-angiogenesis therapies for cancer. Angiogenesis is a cellular process characterized by a number of events, including endothelial cell migration, invasion, and assembly into capillaries. In vitro endothelial tube formation assays are performed using primary human umbilical vein endothelial cells, human aortic endothelial cells, and other human or rodent primary endothelial cells isolated from the vasculature of both tumors and normal tissues. Immortalized endothelial cell lines are also used for these assays. When seeded onto Matrigel, these cells reorganize to create tubelike structure, which may be used as models for studying some aspects of in vitro angiogenesis. Image acquisition by light and fluorescence microscopy and/or quantification of fluorescently labeled cells can be carried out manually or digitally, using commercial software and automated image processing. Here we detail materials, procedure, assay conditions, and cell labeling for quantification of endothelial cell tube formation. This model can be applied to study cellular and molecular mechanisms by which NGF or other neurotrophins promote angiogenesis. This model may also be useful for the development of potential angiogenic and/or anti-angiogenic drugs targeting NGF receptors.
神经生长因子(NGF)是一种神经营养因子,可促进胚胎和成人神经系统中的细胞存活、增殖、分化及神经保护。NGF还可在心血管系统中诱导血管生成效应,这可能有益于构建新血管以及开发新型癌症抗血管生成疗法。血管生成是一个细胞过程,其特征包括多个事件,如内皮细胞迁移、侵袭以及组装成毛细血管。体外内皮管形成试验使用从肿瘤和正常组织脉管系统分离的原代人脐静脉内皮细胞、人主动脉内皮细胞以及其他人类或啮齿动物原代内皮细胞来进行。永生化内皮细胞系也用于这些试验。当接种到基质胶上时,这些细胞会重新组织形成管状结构,这可作为研究体外血管生成某些方面的模型。通过光学显微镜和荧光显微镜进行图像采集和/或对荧光标记细胞进行定量分析,可以手动操作,也可以使用商业软件和自动图像处理进行数字化操作。在此,我们详细介绍用于定量分析内皮细胞管形成的材料、步骤、试验条件及细胞标记方法。该模型可用于研究NGF或其他神经营养因子促进血管生成的细胞和分子机制。该模型也可能有助于开发靶向NGF受体的潜在血管生成和/或抗血管生成药物。