ArticleJournal of Indian Society of Periodontology
Influence of surface texture on osteogenic differentiation of dental pulp stem cells: An
Article in Journal of Indian Society of Periodontology. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
1 citing paper in PubMed.
- Evaluation of periodontal ligament stem cell viability and proliferation on native collagen membranes: AnJournal of Indian Society of PeriodontologyArticle
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Authors and funding
6 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Background: In comparison with perfectly machined surface implants, surface topographic modifications like roughness accelerate the osteogenesis of dental pulpal stem cells (DPSC). This greatly enhances bone-implant contact and osteogenic potential of the stem cells. Hence, the aim of the current study was to evaluate and compare the differentiation and proliferation potential of stem cells obtained from dental pulp on sand-blasted and acid etched implant discs surfaces. Materials and Methods: Stem cells from dental pulp were extracted from the premolar region of oral cavity. Titanium discs that measured one centimeter in diameter and three millimetres in thickness were used as investigation surfaces. Titanium surface disc were acid etched and sandblasted. Investigation had three group: acid etched (Group A), sandblasted (Group B), and standard control group, i.e., cells treated with osteogenic induction media only (Group C). In Group C, mesenchymal stem cells (MSCs) were treated with osteogenic induction medium without any titanium disc and these cells were used as standard controls. To identify which modified implant surface had greater potential for proliferation, 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay was performed using the explant culture. MTT assay assessed the viability of the cells as a function of its redox potential. This was followed by recognition of the stem cells for CD90, CD73, and CD 105 markers using flow cytometry with RUNX2 antibody on days 7 and 21 of incubation. The isolated cells were stained using 1% alizarin red stain to identify the number of stem cells per square centimeter area under the light microscope. Results: The osteogenic differentiation of both the materials was compared with standard control (MSCs treated with osteogenic differentiation media only). The osteoblastic cells on the acid-etched and sand-blasted implant surface disc had an almost identical capacity for proliferation till the MTT assay but according to the results of the alizarin red staining there was a slightly higher proliferation potential on acid etched surfaces compared to the sand blasted surfaces. Therefore, acid etched surfaces showed higher potential of osteogenic differentiation of DPSCs compared with sand-blasted surfaces. Conclusion: In comparison with perfectly machined surface implants, topographic surface modifications such as roughness can accelerate the osteogenesis of DPSC
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