Three-Dimensional Cell Adhesion Matrix
Synthetic biomaterial scaffolds with defined bioactive molecular recognition elements Fine-tunable mechanical properties Purely synthetic and well-characterized reproducible and localized investigation of cell response to biochemical cues
Stem cell maintenance, directed-differentiation, transplant and engraftment Eliciting morphogenic patterns observed in commercially available laminin-rich chemically undefined extracellular matrices Stem cell maintenance, directed-differentiation, transplant and engraftment 3D cell culture Culturing of cognate integrin-expressing tissue types including, but not limited to: endothelial cells embryonic stem cells hematopoietic stem cells and mesenchymal stem cells both non-malignant and malignant human mammary epithelial cells human colon adenocarcinoma
Researchers at the University of California, Davis have invented a series of novel, bioactive, purely synthetic and "made-to-order" cell adhesion matrices which incorporate molecular recognition elements such as cell surface integrin receptor ligands. These biodegradable and biocompatible nanofibrous matrices are advantageous for three-dimensional (3D) tissue culture and tissue engineering. They are comprised of high molecular weight polyvinyl alcohol (PVA) scaffolds functionalized with high-affinity cell adhesion ligands against naturally expressed or cell-transfected integrins, and cross-linked via cyclic complexation of boronic acid crosslinkers with polyhydroxyls on PVA. By using a number of biocompatible modified polymers, researchers can fine-tune the crosslink density and mechanical properties of the matrices. Cell incorporation is achieved by simultaneous encapsulation of cells in situ within the forming matrices, which occurs rapidly at room temperature and physiological pH. Alternatively, cells can be seeded and maintained in culture atop a pre-formed matrix. Extracellular matrices suitable for 3D culture of different cell types can be made to order by combinatorially incorporating a number of molecular recognition elements, such as ligands which target cell-expressed integrins, into the matrix. Finally, crosslinking of the bioactive PVA scaffolds is reversible on demand by the addition of a cis-diol competitor such as fructose, facilitating non-enzymatic degradation of the hydrogel matrix and rapid extraction of cells from 3D culture for other biological applications.
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Related Technologies Additional Technologies by these Inventors Tech ID/UC Case 19575/2009-700-0 Related Cases 2009-700-0
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