In vitro biocompatibility of ICON® and TEGDMA on human dental pulp stem cells

被引:18
|
作者
Goelz, Lina [1 ]
Simonis, Ruth Andrea [2 ]
Reichelt, Joana [2 ]
Stark, Helmut [2 ]
Frentzen, Matthias [3 ]
Allam, Jean-Pierre [4 ]
Probstmeier, Rainer [5 ]
Winter, Jochen [3 ]
Kraus, Dominik [2 ]
机构
[1] Univ Bonn, Ctr Dentomaxillofacial Med, Dept Orthodont, Bonn, Germany
[2] Univ Bonn, Ctr Dentomaxillofacial Med, Dept Prosthodont Preclin Educ & Mat Sci, Welschnonnenstr 17, D-53111 Bonn, Germany
[3] Univ Bonn, Dept Periodontol Operat & Prevent Dent, Bonn, Germany
[4] Univ Bonn, Dept Dermatol & Allergy, Bonn, Germany
[5] Univ Hosp Bonn, Dept Nucl Med, Neuro & Tumor Cell Biol Grp, Bonn, Germany
关键词
ICON (R); Dental pulp stem cell; Resin infiltration; TEDGMA; Cytotoxicity; Inflammation; Biocompatibility; RESIN INFILTRATION; HUMAN GINGIVAL; BONE-MARROW; EXPRESSION; INTERLEUKIN-6; HEMA; QUANTIFICATION; MACROPHAGES; INHIBITION; CULTURE;
D O I
10.1016/j.dental.2016.06.002
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Objectives. Resin infiltrants have been successfully used in dental medicine preventing the progression of tooth decay in an early phase of caries development. ICON (R) is an infiltrant of low-viscosity which penetrates via dentinal tubules into the lesion in dependence of the demineralization depth. Hence, we performed an in vitro study to determine the effect of ICON (R) on human dental pulp stem cells (hDPSCs). Methods. Using explant technique, primary hDPSCs were collected from extracted teeth. Characterization and isolation were performed with typical mesenchymal stem cell markers (Stro-1, CD73, CD90, CD105) and hDPSCs differentiation was validated by immunofluorescence and flow cytometry. HDPSCs were stimulated with light-cured ICON (R) (lc) and non-light-cured ICON (R) (nc) conditioned media as well as different TEGDMA concentrations followed by the analysis of cytotoxicity, pro- and anti-inflammatory responses and differentiation using XTT assay, RT-PCR and ELISAs, respectively. Results. Initial analysis demonstrated that hDPSCs express characteristic mesenchymal stem cell markers and differentiate into adipocytes, chondrocytes and osteoblasts. Notably, ICON (R) nc dramatically reduced cell viability (up to 98.9% after 48 h), whereas ICON (R) lc showed only a modest cytotoxicity (10%). Data were in line with cytokine expression demonstrating increased levels of IL-6 and IL-8 as well as decreased IL-10 after ICON (R) nc exposure compared to ICON (R) lc. ICON (R) lc caused almost no alterations of DSPP, whereas ICON (R) nc markedly elevated DSPP mRNA levels (130.3-times). A concentration-dependent effect was observed in TEGDMA challenged hDPSCs. Significance. ICON (R) is a successful minimal invasive technique. However, clinicians should strictly follow manufacturer's instructions to prevent adverse effects. 2016 The Academy of Dental Materials. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:1052 / 1064
页数:13
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