During this assay, endothelial cells are placed on the upper layer of a cell culture insert with permeable membrane and a solution containing the test agent is placed below the cell permeable membrane. Following an incubation period (3–18 hours), the cells that have migrated through the membrane are stained and counted. The membrane is usually coated with some extracellular matrix component (e.g. collagen) which facilitates both adherence and migration.¹
The main advantage of this assay is its detection sensitivity. Migration through the permeable filter can be caused by very low levels of angiogenic inducers. Prolonged studies are difficult, due to the fact that the test-agent concentration will quickly equalize between the compartment below the membrane and the compartment above the membrane. Another disadvantage is the relative difficulty in setting up the transwells. Commercially available cell culture inserts have alleviated this burden.
- Extracellular Matrices
- Cell Culture Inserts
- Media and Media Supplements
- Cell Dissociation Solutions
- Cell-Permeant Dyes
- Senger D, Perruzzi C, Streit M et al. (2002). The alpha(1)beta(1) and alpha(2)beta(1) integrins provide critical support for vascular endothelial growth factor signaling, endothelial cell migration, and tumor angiogenesis. Am J Pathol. 160(1):195-204.
LT169 updated 6-Oct-2011
For Research Use Only. Not for use in diagnostic procedures.