| Literature DB >> 31565823 |
Stacy Jordahl1, Luis Solorio1, Dylan B Neale1, Sean McDermott1, Jacob H Jordahl1, Alexandra Fox1, Christopher Dunlay1, Annie Xiao2, Martha Brown3, Max Wicha1, Gary D Luker2, Joerg Lahann4.
Abstract
Extracellular matrix (ECM) proteins, and most prominently, fibronectin (Fn), are routinely used in the form of adsorbed pre-coatings in an attempt to create a cell-supporting environment in both two- and three-dimensional cell culture systems. However, these protein coatings are typically deposited in a form which is structurally and functionally distinct from the ECM-constituting fibrillar protein networks naturally deposited by cells. Here, the cell-free and scalable synthesis of freely suspended and mechanically robust three-dimensional (3D) networks of fibrillar fibronectin (fFn) supported by tessellated polymer scaffolds is reported. Hydrodynamically induced Fn fibrillogenesis at the three-phase contact line between air, an Fn solution, and a tessellated scaffold microstructure yields extended protein networks. Importantly, engineered fFn networks promote cell invasion and proliferation, enable in vitro expansion of primary cancer cells, and induce an epithelial-to-mesenchymal transition in cancer cells. Engineered fFn networks support the formation of multicellular cancer structures cells from plural effusions of cancer patients. With further work, engineered fFn networks can have a transformative impact on fundamental cell studies, precision medicine, pharmaceutical testing, and pre-clinical diagnostics.Entities:
Keywords: 3D cell culture; extracellular matrix; fibrillar fibronectin; protein-polymer composites; tumor microenvironment
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Year: 2019 PMID: 31565823 PMCID: PMC6851443 DOI: 10.1002/adma.201904580
Source DB: PubMed Journal: Adv Mater ISSN: 0935-9648 Impact factor: 30.849