| Literature DB >> 27547783 |
Magdalena Angelova1, Heather L Machado2, Kenneth F Swan3, Cindy Morris3, Deborah E Sullivan3.
Abstract
Extravillous trophoblast (EVT) migration and invasion through the decidualized endometrium is essential to successful placentation. SGHPL-4 cells, an EVT cell line derived from first trimester placenta, is a widely used model of cytotrophoblast differentiation into an invasive phenotype. Here we describe a quantitative cell migration assay that can be modified to also measure cell invasion. SGHPL-4 cells were seeded into BD Fluoroblok cell culture inserts constructed with an 8 μm porous membrane and allowed to migrate towards epidermal growth factor, a known chemoattractant for EVTs. To assess EVT invasion, Fluoroblok inserts were first coated with Matrigel, a basement membrane matrix. SGHPL-4 cells were labeled with calcein AM and cells that had invaded and/or migrated across the membrane were quantified by a bottom-reading fluorescence plate reader. The advantage of the Fluoroblok inserts over other migration/invasion assays is that they allow nondestructive detection of migrated cells.Entities:
Year: 2013 PMID: 27547783 PMCID: PMC4991900 DOI: 10.21769/bioprotoc.840
Source DB: PubMed Journal: Bio Protoc ISSN: 2331-8325