Polymers · 2020 · 21 citations · 30 references
EngineeringBioengineeringCell BiologyBiomaterialsRegenerative MedicineTissue EngineeringCell-scaffold InteractionsExtracellular MatrixHydrogelsStem Cell NicheTissue Engineering ScaffoldsTissue Engineering With Stem CellsAdipose Stem Cell NicheAdipose Stem CellsAdipose-derived Mesenchymal Stem CellsAdipose-derived Mesenchymal Stromal CellsHydrogel-based ScaffoldsMesenchymal Stem Cell NicheScaffold BiomaterialsStem Cell Encapsulation
The activity of stem cell processes is regulated by internal and external signals of the cell "niche". In general, the niche of stem cells can be represented as the microenvironment of the cells, providing a signal complex, determining the properties of the cells. At the same time, the "niche" concept implies feedback. Cells can modify their microenvironment, supporting homeostasis or remodeling the composition and structure of the extracellular matrix. To ensure the regenerative potential of tissue engineering products the "niche" concept should be taken into account. To investigate interactions in an experimental niche, an original hydrogel biopolymer scaffold with encapsulated mesenchymal adipose-derived stem cells (ASCs) was used in this study. The scaffold provides for cell adhesion, active cell growth, and proliferative activity. Cells cultured within a scaffold are distinguished by the presence of a developed cytoskeleton and they form a cellular network. ASCs cultured within a scaffold change their microenvironment by secreting VEGF-A and remodeling the scaffold structure. Scaffold biodegradation processes were evaluated after previous culturing of the ASCs in the scaffolds for periods of either 24 h or six days. The revealed differences confirmed that changes had occurred in the properties of scaffolds remodeled by cells during cultivation. The mechanisms of the identified changes and the possibility of considering the presented scaffold as an appropriate artificial niche for ASCs are discussed.
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Structural Basis of Collagen Recognition by Integrin α2β1
Jonas Emsley, Christopher G. Knight, Richard W. Farndale et al. · Cell · 2000 · 994 citations · Full text
Christopher G. Knight, Laurence F. Morton, Anthony R. Peachey et al. · Journal of Biological Chemistry · 2000 · 682 citations · Full text