The plasma membrane abundance of the Na + /K+ pump or Na + ,K+-ATPase depends on the intracellular concentration of Na+ in almost all animal cells. In cartilage, chondrocytes are surrounded by an extracellular matrix which consists of collagen and proteoglycan, a ground substance composed of glycosaminoglycan (GAG) side chains with a high fixed negative charge density. The polyanionic nature of the GAGs tends to draw monovalent cations into the matrix resulting in high [Na + ] which may exceed 250 mM. As the concentration of GAGs in the tissue increases, so does [Na+]. In this study, it was found that the density of the Na+/K+ pump, measured by 3H-ouabain binding, correlates with the concentration of GAGs in the tissue. This indicates that chondrocytes are sensitive to their ionic environment and respond to local [Na + ] variations by regulating the abundance of the Na + /K+ pump.
Poly-(lactide-co-glycolide) (PLGA) is an FDA-approved biodegradable polymer which has been widely used as a scaffold for tissue engineering applications. Collagen has been used as a coating material for bone contact materials, but relatively little interest has focused on biomimetic coating of PLGA with extracellular matrix components such as collagen and the glycosaminoglycan chondroitin sulfate (CS). In this study, PLGA films were coated with collagen type I or collagen I with CS (collagen I/CS) to investigate the effect of CS on the behaviour of the osteoblastic cell line MG 63. Collagen I/CS coatings promoted a significant increase in cell number after 3 days (in comparison to PLGA) and after 7 days (in co mparison to PLGA and collagen-coated PLGA). No influence of collagen I or collagen I/CS coatings on the spreading area after 1 day of culture was observed. However, the cells on collagen I/CS formed numerous filopodia and displayed well developed vinculin-containing focal adhesion plaques. Moreover, thes e cells contained a significantly higher concentration of osteocalcin, measured per mg of protein, than the cells on the pure collagen coating. Thus, it can be concluded that collagen I/CS coatings promote MG 63 cell proliferation, improve cell adhesion and enhance osteogenic cell differentiation., M. Vandrovcová ... [et al.]., and Obsahuje bibliografii a bibliografické odkazy