James Nidhi, Kini Sandya, Pai Swathi, Shenoy Neetha, Kabekkodu Shama Prasada
Department of Conservative Dentistry and Endodontics, MCODS, MAHE, Manipal, Karnataka, India.
Department of Cell and Molecular Biology, School of Life Sciences, MAHE, Manipal, Karnataka, India.
Clin Cosmet Investig Dent. 2022 Apr 5;14:87-94. doi: 10.2147/CCIDE.S314478. eCollection 2022.
The prime factor in determining the success of reimplantation of an avulsed tooth is the maintenance of the viability of periodontal ligament fibroblast cells (PDFC). This study aims to evaluate and compare Mc Carey Kaufman media (MK), Cornisol, Dulbecco's Modified Eagles Medium (DMEM), Hanks Balanced Salt Solution (HBSS) and distilled water in preserving the viability of the PDFC using the Cell Counting Kit-8 assay (CCK-8).
Cryopreserved PDFC were suspended in DMEM and incubated in CO incubator at 370C with 95% humidity and 5% CO for attachment. Once cells attained 80% confluence, they were trypsinised and passed into T-25 culture flasks to expand the culture population. Cells from passage 5 were pooled for experimentation. Trypan blue exclusion test was performed before each experiment to measure cell viability and batches showing more than 95% viability were used in the experiment. The viable PDFC with 1×105 were seeded in 96 well plates and incubated in CO incubator at 370C, 95% humidity and 5% CO for 24 hours to allow cell attachment. A 100µL of the experimental media were added in the wells and the cells were exposed for 1, 24 and 48 hours respectively. The viability was determined using the CCK-8. Experiment was performed in triplicates and data was subjected to statistical analysis.
Statistical analysis was performed using repeated measure ANOVA, ANOVA, and post-hoc Bonferroni test with the significance level p<0.05. The values are as follows: MK (1.3146 ±0.0588, 1.9012±0.0511, 2.0723±0.1211) > Cornisol (1.2399±0.0548, 1.9596±0.0652, 1.9592±0.1361) >DMEM (1.1914±0.0691, 1.8479±0.0116, 2.0718±0.0795) > HBSS (0.3665±0.0814, 0.0184±0.0010, 0.0248±0.0042) >distilled water (0.0122±0.0033, 0.0225±0.0085, 0.0104±0.0008) at 1 hour, 24 hours and 48 hours respectively. MK >Cornisol>DMEM>HBSS>distilled water.
It can be concluded that the corneal preservation solutions showed promising results in preserving periodontal ligament cell viability for extended time periods.
决定脱位牙再植成功的首要因素是维持牙周膜成纤维细胞(PDFC)的活性。本研究旨在使用细胞计数试剂盒-8 检测法(CCK-8)评估和比较麦凯里·考夫曼培养基(MK)、科尼索尔、杜尔贝科改良伊格尔培养基(DMEM)、汉克斯平衡盐溶液(HBSS)和蒸馏水对保存 PDFC 活性的效果。
将冻存的 PDFC 悬浮于 DMEM 中,置于 37℃、湿度 95%、二氧化碳浓度 5%的 CO₂培养箱中孵育以使其贴壁。当细胞达到 80%汇合度时,用胰蛋白酶消化并传代至 T-25 培养瓶以扩大培养群体。将第 5 代细胞合并用于实验。在每次实验前进行台盼蓝排斥试验以测量细胞活性,实验使用活力超过 95%的批次。将 1×10⁵个活的 PDFC 接种于 96 孔板中,置于 37℃、湿度 95%、二氧化碳浓度 5%的 CO₂培养箱中孵育 24 小时以使细胞贴壁。向孔中加入 100µL 实验培养基,细胞分别暴露 1 小时、24 小时和 48 小时。使用 CCK-8 测定细胞活力。实验重复进行三次,数据进行统计分析。
采用重复测量方差分析、方差分析和事后邦费罗尼检验进行统计分析,显著性水平 p<0.05。结果如下:在 1 小时、24 小时和 48 小时时,MK(1.3146±±0.0588,1.9012±±0.0511,2.0723±±0.1211)>科尼索尔(1.2399±± 0.0548,1.9596±±0.0652,1.9592±±0.1361)>DMEM(1.1914±±0.0691,1.8479±±0.0116,2.0718±±0.0795)>HBSS(0.3665±±0.0 814,0.0184±±0.0010,0.0248±±0.0 042)>蒸馏水(0.0122±±0.0033,0.0225±±0.0085,0.0104±±0.0008)。MK>科尼索尔>DMEM>HBSS>蒸馏水。
可以得出结论,角膜保存液在长时间保存牙周膜细胞活力方面显示出有前景的结果。