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富血小板血浆能刺激牙周韧带再生。

An autologous platelet-rich plasma stimulates periodontal ligament regeneration.

机构信息

Private practice, Vitoria, Spain.

出版信息

J Periodontol. 2013 Nov;84(11):1556-66. doi: 10.1902/jop.2013.120556. Epub 2013 Jan 5.

Abstract

BACKGROUND

Regeneration of periodontal tissues is one of the most important goals for the treatment of periodontal disease. The technology of plasma rich in growth factors provides a biologic approach for the stimulation and acceleration of tissue healing. The purpose of this study is to evaluate the biologic effects of this technology on primary human periodontal ligament fibroblasts.

METHODS

The authors studied the response of periodontal ligament cells to this pool of growth factors on cell proliferation, cell migration, secretion of several biomolecules, cell adhesion, and expression of α2 integrin. Cell proliferation and adhesion were evaluated by means of a fluorescence-based method. Cell migration was performed on culture inserts. The release of different biomolecules by periodontal ligament fibroblasts was quantified through enzyme-linked immunosorbent assay. The α2 integrin expression was assessed through Western blot.

RESULTS

This autologous technology significantly stimulated cell proliferation, migration, adhesion, and synthesis of many growth factors from cells including vascular endothelial growth factor, thrombospondin 1, connective tissue growth factor, hepatocyte growth factor, and procollagen type I. The α2 integrin expression was lower in plasma rich in growth factor-treated cells compared to non-stimulated cells, although no statistically significant differences were observed.

CONCLUSION

This plasma rich in growth factors exerts positive effects on periodontal ligament fibroblasts, which could be positive for periodontal regeneration.

摘要

背景

牙周组织再生是牙周病治疗的最重要目标之一。富含生长因子的等离子体技术为刺激和加速组织愈合提供了一种生物学方法。本研究旨在评估该技术对原代人牙周膜成纤维细胞的生物学效应。

方法

作者研究了牙周膜细胞对这种生长因子池的反应,包括细胞增殖、细胞迁移、几种生物分子的分泌、细胞黏附和α2 整合素表达。通过荧光法评估细胞增殖和黏附,通过培养插片评估细胞迁移,通过酶联免疫吸附试验定量测定牙周膜成纤维细胞释放的不同生物分子,通过 Western blot 评估α2 整合素表达。

结果

这种自体技术显著刺激了包括血管内皮生长因子、血小板反应蛋白 1、结缔组织生长因子、肝细胞生长因子和原胶原蛋白 I 在内的细胞的增殖、迁移、黏附和多种生长因子的合成。与未刺激的细胞相比,富含生长因子的等离子体处理后的细胞中α2 整合素表达降低,但无统计学差异。

结论

富含生长因子的等离子体对牙周膜成纤维细胞有积极作用,可能对牙周组织再生有益。

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