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聚己内酯支架作为成骨细胞输送的生物材料:一项体外研究。

Polycaprolactone scaffolds as a biomaterial for cementoblast delivery: An in vitro study.

机构信息

São Leopoldo Mandic Medical and Dental School, Campinas, Brazil.

3D Biotechnology Solutions, Campinas, Brazil.

出版信息

J Periodontal Res. 2022 Oct;57(5):1014-1023. doi: 10.1111/jre.13041. Epub 2022 Aug 5.

Abstract

OBJECTIVE

To define the potential of polycaprolactone (PCL) scaffold for cementoblast delivery.

BACKGROUND

Dental cementum is critical for tooth attachment and position, and its regenerative capabilities remain unpredictable.

METHODS

PCL scaffolds were manufactured by the electrospinning technique at 10% and 20% (w/v) and seeded with cementoblasts (OCCM-30). Scaffolds were characterized for their morphology and biological performance by scanning electron microscopy (SEM), confocal and conventional histology, cytocompatibility (PrestoBlue assay), gene expression (type I collagen - Col1; bone sialoprotein - Bsp; runt-related transcription factor 2 - Runx-2; alkaline phosphatase - Alpl; osteopontin - Opn; osteocalcin - Ocn, osterix - Osx), and the potential to induce extracellular matrix deposition and mineralization in vitro.

RESULTS

Overall, data analysis showed that PCL scaffolds allowed cell adhesion and proliferation, modulated the expression of key markers of cementoblasts, and led to enhanced extracellular matrix deposition and calcium deposition as compared to the control group.

CONCLUSION

Altogether, our findings allow concluding that PCL scaffolds are a viable tool to culture OCCM-30 cells, leading to an increased potential to promote mineralization in vitro. Further studies should be designed in order to define the clinical relevance of cementoblast-loaded PCL scaffolds to promote new cementum formation.

摘要

目的

定义聚己内酯(PCL)支架在成牙骨质细胞递送中的潜力。

背景

牙骨质对于牙齿附着和位置至关重要,但其再生能力仍不可预测。

方法

采用静电纺丝技术在 10%和 20%(w/v)的浓度下制造 PCL 支架,并接种成牙骨质细胞(OCCM-30)。通过扫描电子显微镜(SEM)、共聚焦和常规组织学、细胞相容性(PrestoBlue 测定)、基因表达(I 型胶原 - Col1;骨涎蛋白 - Bsp; runt 相关转录因子 2 - Runx-2;碱性磷酸酶 - Alpl;骨桥蛋白 - Opn;骨钙素 - Ocn、osterix - Osx)来表征支架的形态和生物学性能,并评估其在体外诱导细胞外基质沉积和矿化的能力。

结果

总体而言,数据分析表明,与对照组相比,PCL 支架允许细胞黏附和增殖,调节成牙骨质细胞的关键标志物的表达,并导致细胞外基质沉积和钙沉积增加。

结论

总之,我们的研究结果表明,PCL 支架是培养 OCCM-30 细胞的一种可行工具,可提高体外矿化的潜力。应设计进一步的研究以确定负载有成牙骨质细胞的 PCL 支架促进新牙骨质形成的临床相关性。

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