The Regenerative Effects of Amnion-Chorion Membrane on Bone Marrow Derived Stem Cells.

IF 1.3
Halide Namli Kilic, Yusuke Hamada, Kentaro Imamura, Chandni Batra, Chandler L Walker
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Abstract

The objective of this in vitro study was to evaluate the possible regenerative effects of dehydrated human amnion chorion membrane (ACM) on cell proliferation, migration, and differentiation/mineralization of bone marrow-derived stem cells (BMSCs). The dehydrated human ACM has been commonly used in periodontal regeneration and ridge augmentation procedures due to its membrane properties and growth factors. For the study, commercially available bone marrow-derived stem cells were thawed, cultured, and exposed to different concentrations of amnion-chorion membrane extract (50, 100, 200, 500, and 1000 μg/mL) in mesenchymal stem cell basal media. Cell proliferation was analyzed using the WST-1 assay, migration with the scratch-wound assay, and differentiation/mineralization with Alizarin Red S staining. Two-way ANOVA was used to assess the effects of concentration and time, with pair-wise comparisons made using Fisher protected least significant difference at a 5% significance level. Results showed that the control, 50 μg/mL, and 100 μg/mL groups exhibited lower cell proliferation compared with the 500 μg/mL and 1000 μg/mL groups. Lower concentrations also displayed reduced cell migration compared with the higher concentrations. In the mineralization assay, the control, 200 μg/mL, and 500 μg/mL groups exhibited lower cell mineralization compared with 1000 μg/mL. Temporally, shorter durations showed higher levels of cell migration and lower levels of cell mineralization. Overall, the use of amnion-chorion membrane positively affected cell proliferation, migration, and mineralization, with increased concentrations of amnion-chorion membrane extract yielding greater benefits. This study indicates that amnion-chorion membrane may enhance stem cell activities due to the presence of growth factors in the membrane. These findings are preliminary and must be interpreted cautiously. Further in vivo and clinical studies are necessary to validate these observations.

羊膜-绒毛膜对骨髓干细胞再生的影响。
本体外研究的目的是评估脱水人羊膜(ACM)对骨髓干细胞(BMSCs)细胞增殖、迁移和分化/矿化的可能再生作用。由于其膜特性和生长因子,脱水的人ACM已被广泛用于牙周再生和牙脊增加手术。在这项研究中,将市售的骨髓干细胞解冻、培养,并在间充质干细胞基础培养基中暴露于不同浓度的羊膜-绒毛膜提取物(50、100、200、500和1000 μg/mL)中。用WST-1法分析细胞增殖,用划痕法分析细胞迁移,用茜素红S染色分析细胞分化/矿化。采用双因素方差分析来评估浓度和时间的影响,两两比较使用Fisher在5%显著性水平下保护最小显著差异。结果表明,与500 μg/mL和1000 μg/mL组相比,对照组、50 μg/mL组和100 μg/mL组的细胞增殖能力较低。与高浓度相比,低浓度也显示出细胞迁移减少。在矿化试验中,对照、200 μg/mL和500 μg/mL组细胞矿化程度低于1000 μg/mL组。时间越短,细胞迁移水平越高,细胞矿化水平越低。总的来说,羊膜-绒毛膜的使用对细胞增殖、迁移和矿化有积极的影响,羊膜-绒毛膜提取物浓度的增加产生了更大的好处。本研究提示羊膜-绒毛膜可能由于膜内存在生长因子而增强干细胞活性。这些发现是初步的,必须谨慎解释。需要进一步的体内和临床研究来验证这些观察结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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