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In-vitro cytocompatibility and growth factor content of GBR/GTR membranes

机译:GBR / GTR膜的体外细胞组合和生长因子含量

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Objective. To assess the cytocompatibility of five commercially available xenogenic barrier membranes used for oral regenerative procedures and to determine the growth factor content of these membranes in-vitro.Methods. Human mesenchymal stem cells (hMSCs) and immortalized periodontal ligament stem cells (PDL-hTERTs) were used to determine the cytocompatibility of xenogenic barrier membranes made of collagen (Biogide, BG, Geistlich Pharma AG, Switzerland; Biomend, BM, Zimmer Biomet, USA; Osseoguard OG, Zimmer Biomet, USA; OssixPlus, OX, Datum Dental, Israel) or extracellular matrix (ECM) (Dynamatrix, DM, Keystone Dental, USA) and of their eluates obtained by washing. Cells were cultured with previously washed and unwashed membranes (n=4) and in the medium used for washing (eluate). Cell proliferation at 3 days (eluates) and at 7 days (membranes) was assessed using the WST-1 cell proliferation kit. Growth factor content of the membranes was measured using multiplex ELISA.Results. The eluate of BG and BM significantly inhibited proliferation of hMSCs, whereas DM and OX showed stimulating effects. The highest impact was observed for DM, its eluate doubled the cell proliferation of adherent cells when compared to the control (p0.001). The eluate of OG did not influence eluate cell cultures (p0.05). The presence of membranes had different impact on hMSCs and PDLs. hMSCs seem to be more resistant to the inhibitory effects of BG, OG and BM. hMSCs are only affected by OX, which actually stimulates hMSCs when the specimens are not washed previously. PDLs however proliferate significantly less once they are placed into culture with BM and OG as well as BG-not washed. Once BG is washed no inhibitory effect on PDLs was observed, however overall the washing of membrane samples prior to the placement into the cell culture did hardly have any effect on the outcome. The strongest inhibition of proliferation was shown with the BM and OG membrane in PDL-hTERTs (p0.001). Growth factor contents were quite similar quantitatively and qualitatively among the tested membranes with concentrations in the range of 50-500 pg/ml. Intriguingly DM contained considerably higher amounts of bFGF with up to 8000 pg/ml.Significance. The collagen membranes cross-linked with aldehydes show poor outcomes in PDLs while the collagen membrane cross-linked with polysaccharides generally shows promising results similar to the ECM-membrane DM in both membrane and eluate tests. The findings may be due to various factors, especially differences observed in composition, processing and bFGF content. (C) 2019 The Academy of Dental Materials. Published by Elsevier Inc. All rights reserved.
机译:客观的。评估用于口腔再生步骤的五种商业上可用的异种阻隔膜的细胞织立性,并确定玻璃体中这些膜的生长因子含量。人体间充质干细胞(HMSCs)和永生化的牙周韧带干细胞(PDL-HETTES)用于确定由胶原蛋白制成的异丙族屏障膜的细胞变性(Biogide,BG,Geistlich Pharma Ag,瑞士; BioMend,BM,Zimmer Biomet,USA ; Osseoguard OG,Zimmer Biomet,USA; Ossixplus,牛,基准牙科,以色列)或细胞外基质(ECM)(Mydatrix,DM,Keystone牙科,美国)和通过洗涤获得的洗脱液。用预先洗涤和未洗涤的膜(n = 4)和用于洗涤(洗脱液)的培养基培养细胞。使用WST-1细胞增殖试剂盒评估3天(eluate)和7天(膜)的细胞增殖。使用多重ELISA测量膜的生长因子含量。结果。 BG和BM的洗脱液显着抑制HMSC的增殖,而DM和OX显示出刺激作用。观察到DM的最高影响,其洗脱液与对照相比,粘附细胞的细胞增殖增加了一倍(P <0.001)。 OG的洗脱液不影响eluate细胞培养物(p> 0.05)。膜的存在对HMSC和PDL产生不同的影响。 HMSCs似乎对BG,OG和BM的抑制作用更耐受。 HMSCs仅受牛的影响,这实际上在预先没有洗涤试样时刺激HMSCs。然而,一旦将它们与BM和OG的培养物以及BG-NoT洗涤,就显着较少的较少较少。一旦Bg洗涤,未观察到对PDL的抑制作用,然而,在放置到细胞培养之前,将膜样品的洗涤几乎没有对结果产生任何影响。在PDL-HETTTS中用BM和OG膜显示最强的增殖抑制(P <0.001)。生长因子含量定量和定性在测试的膜中非常相似,浓度在50-500pg / ml的范围内。可感染的DM含有相当大量的BFGF,最高可达8000pg / ml。重要性。与醛交联的胶原膜在PDL中显示出差的结果,而与多糖交联的胶原膜通常显示出与膜和洗脱液测试中的ECM膜DM类似的有希望的结果。结果可能是由于各种因素,特别是在组成,加工和BFGF含量中观察到的差异。 (c)2019年牙科材料学院。由elsevier Inc.出版的所有权利保留。

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