IGF-I和Emdogain对三维支架模型中牙上皮细胞行为的影响

Q4 Dentistry
Maria Johanna Jacoba Heezen, Weibo Zhang, Sara Rudolph, X. Walboomers, P. Yelick
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引用次数: 0

摘要

目的:蛀牙和相关的牙周病仍然是当今社会最常见的慢性疾病。未来,可以通过应用组织工程和再生医学与牙科(TERMD)方法,提供个性化、更有效的治疗选择。一个相关的发现是牙间充质细胞和牙上皮细胞分别再生矿化牙本质和牙釉质组织的潜力。材料和方法:在本研究中,将人牙间充质细胞(hDM)和猪牙上皮细胞(pDE)结合,构建了一个多层生物工程牙芽模型。将hDM细胞接种到聚(ε-己内酯)/聚(丙交酯-乙交酯)(PCL/PLGA)湿电纺支架上,该支架覆盖有从热可逆组织培养板收获的融合pDE细胞片。然后使用这样形成的多层生物工程牙芽在体外培养中研究牙细胞的矿化潜力。据推测,添加介质中可溶性因子胰岛素样生长因子1(IGF-I)和细胞外基质衍生物Emdogain(EMD)将导致分化增强和矿化牙组织形成。用扫描电镜观察支架的孔隙率。组织学和免疫荧光分析证实了hDM细胞在支架、完整的pDE细胞片内的定位,以及连接两者的β-整合素1阳性细胞-细胞连接的存在。结果:扫描电镜显示,EMD尤其能增强pDE细胞的矿化潜能。qRT-PCR分析显示,EMD和IGF-1都显著增强了AMBN的表达,反映了pDE细胞的分化。结论:总之,这些结果证明了EMD和IGF-1在临床前牙组织工程方法中的实用性应被考虑的假设。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The influence of IGF-I and Emdogain on the behavior of dental epithelial cells in a three-dimensional scaffold model
Aim: Tooth decay and associated periodontal disease remain the most common chronic diseases in current society. In the future, individually tailored, more effective therapeutic treatment options could be provided through the application of tissue engineering and regenerative medicine and dentistry (TERMD) approaches. A relevant finding is the potential of both dental mesenchymal and dental epithelial cells to regenerate mineralized dentin and enamel tissues, respectively.Materials and Methods: In the current study, a multi-layered, bioengineered tooth bud model was assembled by combining human dental mesenchymal (hDM) and porcine dental epithelial cells (pDE). The hDM cells were seeded onto poly(epsilon-caprolactone)/ poly (lactide-co-glycolide) (PCL/PLGA) wet electro-spun scaffolds overlayed with confluent pDE cell sheet harvested from thermo-reversible tissue culture plates. The so-formed multi-layered bioengineered tooth bud was then used to study the mineralization potential of the dental cells in in vitro culture. It was hypothesized that the addition of the in media soluble factors Insulin-like growth factor 1 (IGF-I) and the extracellular matrix derivate Emdogain (EMD) would result in enhanced differentiation and mineralized dental tissue formation. Scanning Electron morphological observation was used to characterize scaffolds porosity. Histological and immunofluorescent analyses confirmed the localization of hDM cells inside the scaffold, an intact pDE cell sheet, and the presence of beta-integrin 1-positive cell-cell junctions connecting the two.Results: Scanning Electron Microscopy showed that EMD, in particular, enhanced the mineralization potential of pDE cells. qRT-PCR analyses showed that both EMD and IGF-1 significantly enhanced the expression of Ameloblastin (AMBN), reflecting pDE cell differentiation.Conclusion: In conclusion, these results proved the hypothesis that both EMD and IGF-1 should be considered for their utility in preclinical dental tissue engineering approaches.
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来源期刊
Dentistry 3000
Dentistry 3000 Dentistry-Dentistry (all)
CiteScore
0.40
自引率
0.00%
发文量
25
审稿时长
19 weeks
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