| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 3146632 | Journal of Endodontics | 2014 | 8 Pages |
•Calcium silicate cement facilitates fibronectin and αv subintegrin expression.•Calcium silicate cement releases Si ion–increased fibronectin secretion and adsorption.•Integrin αv small interfering RNA inhibited odontogenic differentiation of human dental pulp cells on calcium silicate.•Calcium silicate cement promotes proliferation and odontogenesis via integrin αv.
IntroductionIt has been proved that integrin αv activity is related to cell proliferation, differentiation, migration, and organ development. However, the biological functions of integrin αv in human dental pulp cells (hDPCs) cultured on silicate-based materials have not been explored. The aim of this study was to investigate the role of integrin αv in the proliferation and odontogenic differentiation of hDPCs cultured with the effect of calcium silicate (CS) cement and β-tricalcium phosphate (TCP) cement.MethodsIn this study, hDPCs were cultured on CS and TCP materials, and we evaluated fibronectin (FN) secretion and integrin αv expression during the cell attachment stage. After small interfering RNA transfection targeting integrin αv, the proliferation and odontogenesis differentiation behavior of hDPCs were analyzed.ResultsThe results indicate that CS releases Si ion–increased FN secretion and adsorption, which promote cell attachment more effectively than TCP. The CS cement facilitates FN and αv subintegrin expression. However, the FN adsorption and integrin expression of TCP are similar to that observed in the control dish. Integrin αv small interfering RNA inhibited odontogenic differentiation of hDPCs with the decreased formation of mineralized nodules on CS. It also down-regulated the protein expression of multiple markers of odontogenesis and the expression of dentin sialophosphoprotein protein.ConclusionsThese results establish composition-dependent differences in integrin binding and its effectiveness as a mechanism regulating cellular responses to biomaterial surface.
