Journal of Biomaterials Science Polymer Edition · 2012 · 14 citations · 34 references
Life SciencesBioengineeringCell BiologyBiomaterialsCell AdhesionStem Cell BiologyAdipocyte DifferentiationBiomaterials For Tissue EngineeringCell MigrationEpithelial-to-mesenchymal TransitionMesenchymal DifferentiationStem Cell PhysiologyAdipogenic DifferentiationAdipose-derived Mesenchymal Stromal CellsAmoeboid MigrationCell Differentiation PotentialDifferentiation PotentialMesenchymal MigrationMesenchymal Stromal Cell MigrationSelf-assembled Monolayers
Microenvironments provide cues to stem cells and induce signals to direct their fate. With a view toward further understanding the correlation between surface chemistry and cell functions of stem cells, adipose-derived stromal cells (ADSCs) and self-assembled monolayers terminated with four different functional groups (-CH3, -NH2, -COOH and -OH) were used to assess cell adhesion, migration and differentiation potential in short-term incubation. Quantitative time-lapse microscopic analysis revealed that migration speed and patterns were strongly regulated by surface chemistry. ADSCs showed a mesenchymal migration pattern on the -COOH-modified surface. In contrast, cells on the -CH3-modified surface displayed an amoeboid-like migration pattern. Cell-migration speeds on the chemically-modified surfaces followed the sequence (by tail-groups): -CH3>-COOH>-OH>-NH2. After 1 day of incubation, ADSCs showed a round compact shape and adipogenic differentiation potential on the -CH3-modified surface. The round compact shape and extremely different migration pattern of ADSCs on -CH3 surfaces were attributed to the lower amount of exposed cell-binding domains of adsorbed proteins. ADSCs exhibited spindle-like shape and higher Collagen II expression on the -COOH-modified surface and well-spread morphology and higher Runx2 expression were observed on the -NH2- and -OH-modified surfaces. Surface chemistry presented a strong influence on cell functions of ADSCs, including cell adhesion, migration and mRNA expression in short-term incubation.
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