University of Medicine and Pharmacy, Faculty of Odonto-Stomatology, Department of Periodontology, Ho Chi Minh City, Vietnam.
J Appl Oral Sci. 2018 Jul 10;26:e20180077. doi: 10.1590/1678-7757-2018-0077.
This study evaluated the influence of platelet-rich plasma (PRP) on the behaviour of human gingival fibroblasts (hGFs), including fibroblast proliferation, migration and colony formation.
PRP was obtained from the human peripheral blood of a healthy volunteer and then was diluted into platelet concentrations of 1%, 2% and 5%. The proliferation of hGFs was determined by two methods: (1) Cell-number counting with a haemocytometer method at days 1, 3, 5 and 7; (2) Colony-forming unit-fibroblast (CFU-F) assay at 2 weeks. The migration of hGFs was evaluated with scratch assay, then recorded digital images were analysed by Image-Analysis J 1.51j8 software to compare the remaining artificial wound areas between PRP groups at 0, 24 and 48 hours.
All hGFs that were cultivated in media with 1%, 2% and 5% PRP showed their ability to proliferate and migrate. Cell numbers incubated with 1% PRP increased significantly during the first three days and peaked at day 5, tending to be similar to their proliferation in complete medium. With concentrations of 2% and 5% PRP, hGFs outgrew and peaked at day 3, which was faster than with those in medium with 1% PRP. Especially, hGFs in the group 5% PRP proliferated with higher cell numbers than those in the other remaining groups at day 3. The hGF colony number that was formed in the group 5% PRP was significantly higher than those in the groups 1% and 2% PRP. Scratch assay showed hGFs in the groups 2% and 5% PRP almost filled the artificial wound and migrated more effectively than in the group 1% PRP at 24 hours, which was significant.
In this study, perhaps the medium with 5% PRP is the dominant option, promoting the abilities of hGFs to heal wounds, because of its fast and effective impact on cell proliferation, colony formation and migration.
本研究评估了富血小板血浆(PRP)对人牙龈成纤维细胞(hGFs)行为的影响,包括成纤维细胞增殖、迁移和集落形成。
从健康志愿者的外周血中获得 PRP,然后将其稀释至血小板浓度为 1%、2%和 5%。通过两种方法测定 hGFs 的增殖:(1)用血细胞计数器法在第 1、3、5 和 7 天计数细胞数;(2)在第 2 周进行集落形成单位-成纤维细胞(CFU-F)测定。用划痕试验评估 hGFs 的迁移,然后用 Image-Analysis J 1.51j8 软件分析记录的数字图像,比较 PRP 组在 0、24 和 48 小时之间的剩余人工伤口面积。
所有在含 1%、2%和 5%PRP 的培养基中培养的 hGFs 均表现出增殖和迁移的能力。孵育 1%PRP 的细胞数量在前三天显著增加,在第 5 天达到高峰,趋于与完全培养基中的增殖相似。在 2%和 5%PRP 的浓度下,hGFs 在第 3 天生长并达到高峰,比在含 1%PRP 的培养基中更快。特别是,在第 3 天,5%PRP 组的 hGF 增殖细胞数量明显高于其他组。5%PRP 组形成的 hGF 集落数明显高于 1%和 2%PRP 组。划痕试验显示,在 24 小时时,2%和 5%PRP 组的 hGFs 几乎填满了人工伤口,比 1%PRP 组迁移得更有效,差异具有统计学意义。
在这项研究中,5%PRP 培养基可能是促进 hGFs 伤口愈合能力的首选,因为它对细胞增殖、集落形成和迁移具有快速而有效的影响。