用于下颌骨缺损重建的水凝胶-壳聚糖和聚乳酸-聚己内酯生物工程支架:临床前体内研究及转化相关方面的评估

M. Ferrari, Stefano Taboni, Harley H. L. Chan, Jason Townson, T. Gualtieri, Leonardo Franz, A. Ruaro, S. Mathews, Michael J. Daly, Catriona M. Douglas, D. Eu, Axel Sahovaler, N. Muhanna, Manuela Ventura, K. Dey, Stefano Pandini, C. Pasini, Federica Re, Simona Bernardi, K. Bosio, D. Mattavelli, F. Doglietto, Shrinidh Joshi, Ralph W. Gilbert, P. Nicolai, S. Viswanathan, L. Sartore, Domenico Russo, Jonathan C. Irish
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摘要

背景:下颌骨缺损的重建是一项外科挑战,微血管重建是目前的金标准。组织生物工程领域为骨重建提供了越来越多的替代策略:在这项临床前研究中,在兔子模型的非临界尺寸下颌骨缺损中探索了两种生物工程支架的性能,一种是由聚乙二醇-壳聚糖(HyCh)制成的水凝胶,另一种是聚(L-乳酸)/聚(ε-己内酯)和HyCh的混合核壳组合(PLA-PCL-HyCh),其中播种了不同浓度的人间质基质细胞(hMSCs)。通过体内放射学检查和体外放射学、组织形态学和免疫组化分析,分析了生物工程支架的骨再生特性:结果:在放置了支架的缺损处,相对密度增加(RDI)明显,尤其是在播种了 hMSCs 的情况下。免疫组化分析表明,在使用支架重建的缺损中,血管内皮生长因子-A和骨桥蛋白的表达量都明显较高。任何实验组均未表现出原生微结构特征:在此,我们证明了支架和种子支架重建可促进骨再生,在 120 天内分别达到手术前骨密度恢复的 50%和 70%,而自发再生的恢复率仅为 40%。虽然再生性能还需要优化,但这些结果将有助于为未来的实验建立基准参考。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Hydrogel-chitosan and polylactic acid-polycaprolactone bioengineered scaffolds for reconstruction of mandibular defects: a preclinical in vivo study with assessment of translationally relevant aspects
Background: Reconstruction of mandibular bone defects is a surgical challenge, and microvascular reconstruction is the current gold standard. The field of tissue bioengineering has been providing an increasing number of alternative strategies for bone reconstruction.Methods: In this preclinical study, the performance of two bioengineered scaffolds, a hydrogel made of polyethylene glycol-chitosan (HyCh) and a hybrid core-shell combination of poly (L-lactic acid)/poly (ε-caprolactone) and HyCh (PLA-PCL-HyCh), seeded with different concentrations of human mesenchymal stromal cells (hMSCs), has been explored in non-critical size mandibular defects in a rabbit model. The bone regenerative properties of the bioengineered scaffolds were analyzed by in vivo radiological examinations and ex vivo radiological, histomorphological, and immunohistochemical analyses.Results: The relative density increase (RDI) was significantly more pronounced in defects where a scaffold was placed, particularly if seeded with hMSCs. The immunohistochemical profile showed significantly higher expression of both VEGF-A and osteopontin in defects reconstructed with scaffolds. Native microarchitectural characteristics were not demonstrated in any experimental group.Conclusion: Herein, we demonstrate that bone regeneration can be boosted by scaffold- and seeded scaffold-reconstruction, achieving, respectively, 50% and 70% restoration of presurgical bone density in 120 days, compared to 40% restoration seen in spontaneous regeneration. Although optimization of the regenerative performance is needed, these results will help to establish a baseline reference for future experiments.
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