By L. Baeakova;V. Ivoreik
Cell-material interface performs a key function within the interplay of cells with synthetic fabrics designed for development of physique implants or tissue engineering. actual and chemical homes of the fabric floor, resembling its polarity, wettability, electric cost and conductivity, roughness and morphology, pressure or elasticity in addition to the presence of assorted chemical sensible teams, strongly effect the cellphone adhesion. The latter is mediated by way of adsorption of cellphone adhesion-mediating molecules (eg: vitronectin, fibronectin, collagen, laminin, fibrinogen) from the serum of the tradition medium or physique fluids in acceptable spatial conformation or flexibility allowing the accessibility of particular websites on those molecules (eg: definite amino acid sequences or saccharide-based ligands) by means of adhesion receptors at the cellphone membrane (eg: integrins).After binding those ligands, the adhesion receptors are recruited into focal adhesion plaques, the place they go along with cascades of varied structural and signalling molecules, reminiscent of cytoskeletal proteins and kinases. via those cascades, the sign supplied by means of the cell-material interplay is dropped at the mobile nucleus. It affects the gene expression, and therefore the extra habit of cells, manifested by means of their viability, synthesis of varied molecules, proliferation, differentiation, functioning, immune activation, pressure version or phone death.This interdisciplinary evaluation comprises: actual alterations of the fabric floor via plasma discharge, irradiation with ions or ultraviolet gentle and results of those adjustments at the floor wettability, electric conductivity and formation of chemical practical teams influencing telephone adhesion; deposition of natural or inorganic layers at the fabric surfaces, specifically these nanostructured (eg: nanofibers of fibrin and extracellular matrix molecules, carbon nanoparticles, reminiscent of nanodiamonds, fullerenes and nanotubes, nanocomposite metal/C:H layers); functionalisation of the cloth floor with amino acids and oligopeptidic ligands for mobile adhesion receptors (e.g., GRGDSG); and, influence of a majority of these adjustments at the quantity and power of adhesion of vascular and bone-derived cells, phone proliferation job, swap among phone proliferation and differentiation, expression of cell-type particular markers of differentiation and different telephone capabilities.
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Additional info for Cell Colonization Control Physical and Chemical Modification of Materials
In Table 4, the concentration of detected groups -CH2-, -C-O-, -C=O and -OC=O is presented [78,82]. One can see that during sample aging the concentration of -C=O group increases and -O-C=O decreases. Only a trace concentration of nitrogen was detected. Bačáková and V. Švorčík Figure 10. The XPS survey spectra of PE modified by plasma (plasma/PE) or modified by plasma and water etched (H2O/plasma/PE) measured 24 h after the plasma treatment. Before the measurement the samples were stored under standard laboratory conditions.
Detailed comment of EPR observation (“aging” of radicals) is described too . Figure 9. Concentration depth profiles of oxygen obtained from RBS measurement of plasma-treated PE and that of plasma-treated and water etched for 24 hours . C (1s) a O (1s) concentrations (at. %) determined from XPS measurements and radical densities (R, 1018 g-1) determined by EPR method. The concentrations and densities were determined on the pristine PE, plasma-treated PE (1 or 24 hours after the treatment) and plasma-treated and water etched PE (see left hand side of the table).
1 hour after plasma treatment. One can see from Table 3 that with increasing aging time the oxygen concentration decreases due to rearrangement of the treated polymer chains and their fragments [74,81]. The profile and area of individual peak in XPS spectra enable to determine chemical group concentration in PE surface (see Table 4). Model deconvoluted C(1s) peak is shown in Figure 11. In Table 4, the concentration of detected groups -CH2-, -C-O-, -C=O and -OC=O is presented [78,82]. One can see that during sample aging the concentration of -C=O group increases and -O-C=O decreases.