dc.contributor | University of Michigan | |
dc.contributor | Universidade Estadual Paulista (Unesp) | |
dc.contributor | University of the Pacific | |
dc.date.accessioned | 2014-05-27T11:27:28Z | |
dc.date.available | 2014-05-27T11:27:28Z | |
dc.date.created | 2014-05-27T11:27:28Z | |
dc.date.issued | 2013-01-01 | |
dc.identifier | Dental Materials, v. 29, n. 1, p. 97-102, 2013. | |
dc.identifier | 0109-5641 | |
dc.identifier | http://hdl.handle.net/11449/74169 | |
dc.identifier | 10.1016/j.dental.2012.08.002 | |
dc.identifier | WOS:000312269000008 | |
dc.identifier | 2-s2.0-84871014475 | |
dc.description.abstract | Objectives: The clinical translation of stem cell-based Regenerative Endodontics demands further development of suitable injectable scaffolds. Puramatrix™ is a defined, self-assembling peptide hydrogel which instantaneously polymerizes under normal physiological conditions. Here, we assessed the compatibility of Puramatrix™ with dental pulp stem cell (DPSC) growth and differentiation. Methods: DPSC cells were grown in 0.05-0.25% Puramatrix™. Cell viability was measured colorimetrically using the WST-1 assay. Cell morphology was observed in 3D modeling using confocal microscopy. In addition, we used the human tooth slice model with Puramatrix™ to verify DPSC differentiation into odontoblast-like cells, as measured by expression of DSPP and DMP-1. Results: DPSC survived and proliferated in Puramatrix™ for at least three weeks in culture. Confocal microscopy revealed that cells seeded in Puramatrix™ presented morphological features of healthy cells, and some cells exhibited cytoplasmic elongations. Notably, after 21 days in tooth slices containing Puramatrix™, DPSC cells expressed DMP-1 and DSPP, putative markers of odontoblastic differentiation. Significance: Collectively, these data suggest that self-assembling peptide hydrogels might be useful injectable scaffolds for stem cell-based Regenerative Endodontics. © 2012 Academy of Dental Materials. | |
dc.language | eng | |
dc.relation | Dental Materials | |
dc.relation | 4.039 | |
dc.relation | 2,106 | |
dc.rights | Acesso restrito | |
dc.source | Scopus | |
dc.subject | Dental pulp | |
dc.subject | Hydrogel | |
dc.subject | Odontoblast | |
dc.subject | Regenerative Endodontics | |
dc.subject | Stem cells | |
dc.subject | Tissue engineering | |
dc.subject | 3-d modeling | |
dc.subject | Cell morphology | |
dc.subject | Cell viability | |
dc.subject | Cell-based | |
dc.subject | Clinical translation | |
dc.subject | Human teeths | |
dc.subject | Hydrogel scaffolds | |
dc.subject | Injectable scaffolds | |
dc.subject | Morphological features | |
dc.subject | Physiological condition | |
dc.subject | PuraMatrix | |
dc.subject | Self-assembling peptides | |
dc.subject | Cell culture | |
dc.subject | Confocal microscopy | |
dc.subject | Dentistry | |
dc.subject | Hydrogels | |
dc.subject | Scaffolds (biology) | |
dc.title | A hydrogel scaffold that maintains viability and supports differentiation of dental pulp stem cells | |
dc.type | Artículos de revistas | |