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在体外条件培养基对 3 种不同细胞系的影响,这些细胞系与牙种植学有关。

In vitro effects of Choukroun's platelet-rich fibrin conditioned medium on 3 different cell lines implicated in dental implantology.

机构信息

Equipe de Biomatériaux en Site Osseux, UMR CNRS 6226, Sciences Chimiques de Rennes, Faculté d'Odontologie, Université de Rennes 1, Université Européenne de Bretagne, Rennes Cedex, France.

出版信息

Implant Dent. 2012 Feb;21(1):51-6. doi: 10.1097/ID.0b013e31822b9cb4.

Abstract

OBJECTIVE

The aim of this work was to determine the relevance of Choukroun's platelet-rich fibrin (PRF) in dental implantology by determining the in vitro effects of soluble factors released by PRF clot. We used 3 different cell lines implicated in dental implantology: osteoblast, keratinocyte, and fibroblast.

METHODS

Cellular viability, cell proliferation, and gene expression were analyzed using PRF conditioned medium. Three different cells lines were used: SaOS2 (osteoblast), MRC5 (fibroblast), and KB (epithelial cell).

RESULTS

The sulforhodamine B assay showed a significant increase in cell number for the undiluted and 1:3 diluted conditioned medium after 24 and 48 hours. There was no effect for the 1:9 dilution. Cell cycle analysis by flow cytometry confirmed the viability test results. After 48 hours, PRF conditioned medium induced gene expression in osteoblasts. Expression of osteopontin and osteocalcin, late osteogenic markers, was observed using reverse transcriptase-polymerase chain reaction (RT-PCR).

CONCLUSIONS

This study establishes a model to evaluate, in vitro, the effects of soluble growth factors released by PRF clot. Our work confirmed PRF is useful in stimulating tissue healing and bone regeneration. This work should recommend Choukroun's PRF in numerous implantology clinical applications.

摘要

目的

本研究旨在通过确定富血小板纤维蛋白(PRF)凝块释放的可溶性因子的体外作用,来确定 Choukroun 的 PRF 在牙科种植体中的相关性。我们使用了 3 种与牙科种植体相关的不同细胞系:成骨细胞、角质形成细胞和成纤维细胞。

方法

使用 PRF 条件培养基分析细胞活力、细胞增殖和基因表达。使用了 3 种不同的细胞系:SaOS2(成骨细胞)、MRC5(成纤维细胞)和 KB(上皮细胞)。

结果

磺酰罗丹明 B 检测显示,在稀释 24 和 48 小时后,未稀释和稀释 1:3 的条件培养基中的细胞数量明显增加。稀释 1:9 时无影响。通过流式细胞术进行细胞周期分析证实了活力测试结果。48 小时后,PRF 条件培养基诱导成骨细胞基因表达。使用逆转录-聚合酶链反应(RT-PCR)观察到晚期成骨标志物骨桥蛋白和骨钙素的表达。

结论

本研究建立了一种体外评估 PRF 凝块释放的可溶性生长因子作用的模型。我们的工作证实了 PRF 可有效刺激组织愈合和骨再生。这项工作应该会推荐 Choukroun 的 PRF 在众多种植体临床应用中使用。

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