Titolo | Long-term fluoride release from dental resins affects STRO-1+ cell behavior |
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Tipo di pubblicazione | Articolo su Rivista peer-reviewed |
Anno di Pubblicazione | 2015 |
Autori | Calarco, A., Di Salle A., Tammaro Loredana, De Luca I., Mucerino S., Petillo O., Riccitiello F., Vittoria V., and Peluso G. |
Rivista | Journal of Dental Research |
Volume | 94 |
Paginazione | 1099-1105 |
ISSN | 00220345 |
Parole chiave | aluminum hydroxide, anticaries agent, Artificial, Cariostatic Agents, cell culture, cell differentiation, cell motion, Cell Movement, Cells, chemistry, Chemokine CXCL12, Cultured, CXCL12 protein, cytology, dental material, Dental Materials, Dental Pulp, dentin sialophosphoprotein, DMP1 protein, drug effects, Extracellular Matrix Proteins, fluoride, Fluorides, glycoprotein, Glycoproteins, human, Humans, hydrotalcite, Kinetics, magnesium hydroxide, MEPE protein, metabolism, Odontogenesis, osteocalcin, Phenotype, phosphoprotein, Phosphoproteins, real time polymerase chain reaction, Real-Time Polymerase Chain Reaction, Saliva, saliva substitute, scleroprotein, sialoglycoprotein, Sialoglycoproteins, stem cell, Stem cells, stromal cell derived factor 1, tooth development, tooth pulp, transforming growth factor beta1 |
Abstract | Fluoride-releasing restorative dental materials can be beneficial to remineralize dentin and help prevent secondary caries. However, the effects of fluoride release from dental materials on the activity of dental pulp stem cells are not known. Here we investigate whether different fluoride release kinetics from dental resins supplemented with modified hydrotalcite (RK-F10) or fluoride-glass filler (RK-FG10) could influence the behavior of a human dental pulp stem cell subpopulation (STRO-1+ cells) known for its ability to differentiate toward an odontoblast-like phenotype. The 2 resins, characterized by similar physicochemical properties and fluoride content, exhibited different long-term fluoride release kinetics. Our data demonstrate that long-term exposure of STRO-1+ cells to a continuous release of a low amount of fluoride by RK-F10 increases their migratory response to transforming growth factor β1 (TGF-β1) and stromal cell-derived factor 1 (SDF-1), both important promoters of pulp stem cell recruitment. Moreover, the expression patterns of dentin sialoprotein (dspp), dentin matrix protein 1 (dmp1), osteocalcin (ocn), and matrix extracellular phosphoglycoprotein (mepe) indicate a complete odontoblast-like cell differentiation only when STRO-1+ cells were cultured on RK-F10. On the contrary, RK-FG10, characterized by an initial fluoride release burst and reduced lifetime of the delivery, did not elicit any significant effect on both STRO-1+ cell migration and differentiation. Taken together, our results highlight the importance of taking into account fluoride release kinetics in addition to fluoride concentration when designing new fluoride-restorative materials. © International & American Associations for Dental Research. |
Note | cited By 0 |
URL | https://www.scopus.com/inward/record.uri?eid=2-s2.0-84937962299&doi=10.1177%2f0022034515584615&partnerID=40&md5=85d7d282f1751a76ab4c37a9d072441f |
DOI | 10.1177/0022034515584615 |
Citation Key | Calarco20151099 |