Francescone Ralph A, Faibish Michael, Shao Rong
Molecular and Cellular Biology Program, Morrill Science Center, University of Massachusetts, USA.
J Vis Exp. 2011 Sep 7(55):3040. doi: 10.3791/3040.
Over the past several decades, a tube formation assay using growth factor-reduced Matrigel has been typically employed to demonstrate the angiogenic activity of vascular endothelial cells in vitro. However, recently growing evidence has shown that this assay is not limited to test vascular behavior for endothelial cells. Instead, it also has been used to test the ability of a number of tumor cells to develop a vascular phenotype. This capability was consistent with their vasculogenic behavior identified in xenotransplanted animals, a process known as vasculogenic mimicry (VM). There is a multitude of evidence demonstrating that tumor cell-mediated VM plays a vital role in the tumor development, independent of endothelial cell angiogenesis. For example, tumor cells were found to participate in the blood perfused, vascular channel formation in tissue samples from melanoma and glioblastoma patients. Here, we described this tubular network assay as a useful tool in evaluation of vasculogenic activity of tumor cells. We found that some tumor cell lines such as melanoma B16F1 cells, glioblastoma U87 cells, and breast cancer MDA-MB-435 cells are able to form vascular tubules; but some do not such as colon cancer HCT116 cells. Furthermore, this vascular phenotype is dependent on cell numbers plated on the Matrigel. Therefore, this assay may serve as powerful utility to screen the vascular potential of a variety of cell types including vascular cells, tumor cells as well as other cells.
在过去几十年中,一种使用生长因子减少的基质胶进行的管形成试验通常被用于在体外证明血管内皮细胞的血管生成活性。然而,最近越来越多的证据表明,该试验不仅限于测试内皮细胞的血管行为。相反,它也被用于测试许多肿瘤细胞形成血管表型的能力。这种能力与它们在异种移植动物中确定的血管生成行为一致,这一过程被称为血管生成拟态(VM)。有大量证据表明,肿瘤细胞介导的VM在肿瘤发展中起着至关重要的作用,独立于内皮细胞血管生成。例如,在黑色素瘤和胶质母细胞瘤患者的组织样本中发现肿瘤细胞参与了血液灌注的血管通道形成。在这里,我们将这种管状网络试验描述为评估肿瘤细胞血管生成活性的一种有用工具。我们发现一些肿瘤细胞系,如黑色素瘤B16F1细胞、胶质母细胞瘤U87细胞和乳腺癌MDA-MB-435细胞能够形成血管小管;但有些则不能,如结肠癌HCT116细胞。此外,这种血管表型取决于接种在基质胶上的细胞数量。因此,该试验可作为一种强大的工具,用于筛选包括血管细胞、肿瘤细胞以及其他细胞在内的多种细胞类型的血管生成潜力。