Trevigen, Gaithersburg, Maryland, USA.
Nat Protoc. 2010 Apr;5(4):628-35. doi: 10.1038/nprot.2010.6. Epub 2010 Mar 11.
A protocol is presented here for a rapid, quantitative and reliable in vitro angiogenesis assay that can be adapted for high throughput use. Endothelial cells are plated on a gelled basement matrix, their natural substrate, and form capillary-like structures with a lumen. The assay can be used to identify inhibitors or stimulators of angiogenesis, as well as genes and signaling pathways involved in angiogenesis. It has also been used to identify endothelial progenitor cells. This assay involves endothelial cell adhesion, migration, protease activity and tubule formation. This tube formation assay is preferred, as other in vitro assays for angiogenesis, such as cell adhesion, migration and invasion, measure limited steps in the angiogenesis process. The tube formation assay on basement membrane can be completed in a day because transformed endothelial cells form tubes within 3 h, whereas non-transformed endothelial cells form tubes within 6 h.
这里提出了一种快速、定量和可靠的体外血管生成分析方法,可适用于高通量应用。内皮细胞铺在凝胶基底基质上,这是它们的天然基质,并形成带有腔的毛细血管样结构。该分析方法可用于鉴定血管生成的抑制剂或刺激剂,以及参与血管生成的基因和信号通路。它也被用于鉴定内皮祖细胞。该分析方法涉及内皮细胞黏附、迁移、蛋白酶活性和管状结构形成。由于其他体外血管生成分析方法,如细胞黏附、迁移和侵袭,仅测量血管生成过程中的有限步骤,因此该管状结构形成分析方法更受欢迎。基底膜上的管状结构形成分析可在一天内完成,因为转化的内皮细胞在 3 小时内形成管状结构,而非转化的内皮细胞在 6 小时内形成管状结构。