Endothelial Cell Tube Formation Assay for the <em>In Vitro</em> Study of Angiogenesis
Author(s) -
Kathleen L. DeCicco-Skinner,
Gervaise H. Henry,
Christophe Cataisson,
Tracy Tabib,
J. Curtis Gwilliam,
Nicholas Watson,
Erica M. Bullwinkle,
Lauren Falkenburg,
Rebecca O’Neill,
Adam Morin,
Jonathan S. Wiest
Publication year - 2014
Publication title -
journal of visualized experiments
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.596
H-Index - 91
ISSN - 1940-087X
DOI - 10.3791/51312
Subject(s) - angiogenesis , basement membrane , microbiology and biotechnology , in vitro , confocal microscopy , extracellular matrix , confocal , endothelial stem cell , neovascularization , wound healing , biology , in vivo , chemistry , fluorescence microscope , biophysics , immunology , cancer research , fluorescence , biochemistry , optics , physics
Angiogenesis is a vital process for normal tissue development and wound healing, but is also associated with a variety of pathological conditions. Using this protocol, angiogenesis may be measured in vitro in a fast, quantifiable manner. Primary or immortalized endothelial cells are mixed with conditioned media and plated on basement membrane matrix. The endothelial cells form capillary like structures in response to angiogenic signals found in conditioned media. The tube formation occurs quickly with endothelial cells beginning to align themselves within 1 hr and lumen-containing tubules beginning to appear within 2 hr. Tubes can be visualized using a phase contrast inverted microscope, or the cells can be treated with calcein AM prior to the assay and tubes visualized through fluorescence or confocal microscopy. The number of branch sites/nodes, loops/meshes, or number or length of tubes formed can be easily quantified as a measure of in vitro angiogenesis. In summary, this assay can be used to identify genes and pathways that are involved in the promotion or inhibition of angiogenesis in a rapid, reproducible, and quantitative manner.
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