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Dent Mater J ; 37(2): 197-205, 2018 Mar 30.
Article in English | MEDLINE | ID: mdl-29415969

ABSTRACT

Titanium surface modification is critical for dental implant success. Our aim was to determine surfaces influence on dental pulp stem cells (DPSCs) viability and differentiation. Implants were divided into sandblasted/acid-etched (control) and sandblasted/acid-etched coated with calcium and magnesium ions (CaMg), supplied as composite (test). Proliferation was evaluated by MTT, differentiation checking osteoblastic gene expression, PGE2 secretion and matrix formation, inflammation by Interleukin 6 (IL-6) detection. MTT and IL-6 do not modify on test. A PGE2 increase on test is recorded. BMP2 is higher on test at early experimental points, Osterix and RUNX2 augment later. Alizarin-red S reveals higher matrix production on test. These results suggest that test surface is more osteoinductive, representing a start point for in vivo studies aiming at the construction of more biocompatible dental implants, whose integration and clinical performance are improved and some undesired effects, such as implant stability loss and further surgical procedures, are reduced.


Subject(s)
Dental Pulp/cytology , Osteoblasts/cytology , Stem Cells/cytology , Titanium/chemistry , Acid Etching, Dental , Calcium/chemistry , Cell Culture Techniques , Cell Differentiation , Cell Proliferation , Cell Survival , Cells, Cultured , Dental Pulp/metabolism , Dinoprostone/metabolism , Enzyme-Linked Immunosorbent Assay , Flow Cytometry , Humans , In Vitro Techniques , Interleukin-6/metabolism , Magnesium/chemistry , Materials Testing , Microscopy, Electron, Scanning , Polymerase Chain Reaction , Stem Cells/metabolism , Surface Properties
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