两种血小板浓缩物(a-PRF和L-PRF)对成骨前MG-63细胞活性影响的体外比较研究

Azadeh Esmaeilnejad, Mohammadreza Talebi Ardakani, Mahdi Shokri, PhD Nima Hosseini Khou, Mobina Kamani
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引用次数: 3

摘要

问题陈述:目前,用新的血小板浓缩物重建骨缺损被认为是牙周病的一个重大挑战。目的:探讨先进富血小板纤维蛋白(A-PRF)和白细胞富血小板纤维蛋白(L-PRF)对MG-63细胞增殖分化的影响。材料与方法:在体外实验中,采集5名健康非吸烟志愿者的血液样本,按照Choukroun和Ghanaati两种方案立即离心,不添加任何抗凝剂,制备L-PRF和A-PRF。在将凝块冷冻一小时后,将其粉碎并再次离心。培养MG-63细胞后,分别采用甲基噻唑四氮唑(MTT)法和茜素红染色法评价浓度为20%、10%、1%和0.5%的A-PRF和L-PRF提取物对细胞增殖和矿化的影响。结果:总体而言,L-PRF组在两个时间间隔内的存活和增殖均高于A-PRF组,且随提取物浓度的增加而增加。然而,在A-PRF组中,不同浓度之间没有显著差异,只是细胞数量随时间增加。3天后,在矿化研究中,仅阳性对照组(成骨组)观察到结节形成。在7 d内,不同浓度A-PRF组均形成矿化结节,而L-PRF组均未形成矿化结节。结论:L-PRF能促进MG-63细胞的增殖,a - prf对MG-63细胞的分化有积极作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Comparative Evaluation of the Effect of Two Platelet Concentrates (a-PRF and L-PRF) on the Cellular Activity of Pre-osteoblastic MG-63 Cell Line: An in vitro Study.

Comparative Evaluation of the Effect of Two Platelet Concentrates (a-PRF and L-PRF) on the Cellular Activity of Pre-osteoblastic MG-63 Cell Line: An in vitro Study.

Statement of the problem: Currently, the reconstruction of bone defects with new platelet concentrates is considered a significant challenge in periodontics.

Purpose: This study aimed to evaluate advanced- platelet rich fibrin (A-PRF) and leukocyte- and platelet rich fibrin's (L-PRF) effects on the proliferation and differentiation of MG-63 cells.

Materials and method: In this in vitro study, blood samples of five healthy non-smoking volunteers were collected and immediately centrifuged according to the two protocols of Choukroun and Ghanaati, without adding any anticoagulants, to prepare L-PRF and A-PRF. After freezing the clots for one hour, they were crushed and centrifuged once more. After culturing MG-63 cells, the effects of 20%, 10%, 1%, and 0.5% concentrations of A-PRF and L-PRF extracts on cell proliferation and mineralization were evaluated by methyl thiazolyl tetrazolium (MTT) assay and Alizarin Red staining, respectively.

Results: Generally, survival and proliferation in the L-PRF group at both time intervals were higher than the A-PRF group and increased with increasing the extract concentration. However, in the A-PRF group, there were no significant differences between the different concentrations, and only the number of cells increased over time. After three days, in the study on mineralization, nodule formation was observed only in the positive control group (osteogenic). In seven days, mineralized nodules were formed in all groups with different concentrations of A-PRF, but not in any of the L-PRF groups.

Conclusion: According to the results, L-PRF increased proliferation, and A-PRF exerted a positive effect on the differentiation of MG-63 cells.

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