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Attachment, proliferation and collagen type I mRNA expression of human gingival fibroblasts on different biodegradable membranes

机译:人牙龈成纤维细胞在不同生物可降解膜上的附着,增殖和I型胶原mRNA表达

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The purpose of this study was to investigate adhesion, proliferation and type I collagen (COL I) mRNA expression of gingival fibroblasts on different membranes used in periodontal applications. Collagen (C), acellular dermal matrix (ADM) and polylactic acid; polyglycolic acid; lactide/glycolide copolymer (PLGA) biodegradable membranes were combined with gingival fibroblasts in culture and incubated for 48 h. Cell adhesion was examined with scanning electron and confocal microscopy. MTT assay was used to measure proliferation. COL I mRNA expression was assessed using quantitative-polymerase chain reaction (QPCR). The PLGA group exhibited the lowest cell survival on day 5 and 10, and lowest cell proliferation on days 5, 10 and 14. While cell proliferation was similar in C and ADM groups, the C membrane showed a slightly greater increase in viable cells to day 10. Confocal and scanning electron microscopy confirmed the results of proliferation and MTT assays. The highest COL I mRNA expression was noted in the PLGA membrane group when compared to the C (p<0.01) and ADM (p<0.05) membrane groups. These data revealed that adherence and proliferation of primary gingival fibroblasts on collagen-based C and ADM membranes is better than that seen with PLGA membranes, and thus may be preferable in the treatment of gingival recession defects.
机译:这项研究的目的是调查牙周应用中不同膜上牙龈成纤维细胞的粘附,增殖和I型胶原(COL I)mRNA表达。胶原蛋白(C),无细胞真皮基质(ADM)和聚乳酸;聚乙醇酸丙交酯/乙交酯共聚物(PLGA)可生物降解的膜与牙龈成纤维细胞结合培养,孵育48小时。用扫描电子和共聚焦显微镜检查细胞粘附。使用MTT测定法测量增殖。使用定量聚合酶链反应(QPCR)评估COL I mRNA表达。 PLGA组在第5天和第10天表现出最低的细胞存活率,而在第5天,第10和14天表现出最低的细胞增殖。尽管C和ADM组的细胞增殖相似,但C膜显示到第3天存活细胞的增长略大10.共聚焦和扫描电子显微镜证实了增殖和MTT测定的结果。与C(p <0.01)和ADM(p <0.05)膜组相比,PLGA膜组的COL I mRNA表达最高。这些数据表明,主要的牙龈成纤维细胞在胶原基C和ADM膜上的粘附和增殖要好于PLGA膜,因此在治疗牙龈退缩缺陷方面可能是优选的。

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