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Scaffolds interactions

Fabrication approaches have been previously used in two-dimensional (2D) micropattemed model systems and have led to insights on the effect of cell-cell and cell-polymer scaffold interactions on hepatocyte and endothelial cell fate. Extending these studies, the application of 3D fabrication techniques may also prove useful for studying structure-function relationships in model tissues. [Pg.144]

Enhancing tissue regeneration by controlling cell-scaffold interaction and the necessity to accommodate cellular metabolic demands through scaffold diffusivity were two fundamental scaffold-design requirements enunciated in the early 1990s (Cima et ah, 1991 Langer et ah, 1990). [Pg.109]

Cell-cell interactions and cell-scaffold interactions have been shown to unprove viability and stabilize function. Complete understanding of the mechanisms required to stabilize hepatocyte function will have a broad impact on this technology. [Pg.148]

Much of the plethora of new research in cell-scaffold interactions should be considered in the development of the ideal scaffold. The implementation of these new technologies will depend on the incorporation and preferably covalent binding of the receptor and the maintenance of its activity during the culmring process. ... [Pg.154]

Similar scaffolding interactions occur in the cocatalytic sites of aminopeptidases as well (Table 2). A second type of interaction occurs in many of these sites. When only one of the oxygens of an Asp or Glu ligand binds the metal the other oxygen forms a H-bond with a Ser or Gin or its isosteric amino acid His. The particular type of interactions are again highly conserved and characteristic of the class of peptidase. [Pg.5143]

The C-terminal loop in cupredoxins holding three of the copper ligands vary in length for the different cupredoxins. Cupredoxin chimeras have been generated where the C-terminal copper-binding loop of another cupredoxin has been grafted into the protein scaffold of another cupredoxin (for a recent review see Dennison ). These studies demonstrate the importance of loop-scaffold interactions for metal sites in cupredoxins and generally in proteins. [Pg.494]

Shot L, Guceri S, Wen X et al (2007) Fabrication of three-dimensional polycaprolactone/ hydroxyapatite tissue scaffolds and osteoblast-scaffold interactions in vitro. Biomaterials 28 5291-5297... [Pg.73]

Shastri, V. R., and Danger, R., Fabrication and biocompatibility of 3-D conductive scaffolds interactive scaffolds for. stimulated tissue regeneration and tissue engineering, in preparation. [Pg.1049]

Figure 19.2 Microparticles implanted in the infarcted myocardium of a rat myocardial infarction model. The bioresorbable scaffold interacts with the host tissue, modulating macrophage polarization through the recruitment of antiinflammatory M2 macrophages and favoring tissue recovery. PLGA MP, poly(lactic-co-glycolic acid)-microparticle. Figure 19.2 Microparticles implanted in the infarcted myocardium of a rat myocardial infarction model. The bioresorbable scaffold interacts with the host tissue, modulating macrophage polarization through the recruitment of antiinflammatory M2 macrophages and favoring tissue recovery. PLGA MP, poly(lactic-co-glycolic acid)-microparticle.
Hydrogels are 3D networks of polymeric chains which are formed via covalent or noncovalent cross-linking reactions. They provide a favorable environment for cell growth due to high biocompatibility and could be used as an injectable format to fill tissue defects. Moreover, many hydrogels are resistant to nonspecific protein adsorption and therefore have been widely studied as potential platforms for the incorporation of proteins and peptides in ECM to control cell-scaffolds interactions. The capability to absorb large amounts of water allows for the entrapment and sustainability of the release of growth... [Pg.224]

Bashor, C.J., Helman, N.C., Yan, S., and Lim, W.A. 2008. Using engineered scaffold interactions to reshape MAP kinase pathway signaling dynamics. Science 319 1539-1543. [Pg.642]


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See also in sourсe #XX -- [ Pg.527 ]




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