Reconstruction du cartilage nasal par ingénierie tissulaire à base de polyéthylène de haute densité et d’un hydrogel

M. Durbec , N. Mayer , D. Vertu-Ciolino , F. Disant , F. Mallein-Gerin , E. Perrier-Groult
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引用次数: 7

Abstract

Aim of the study

Nasal reconstruction remains a challenge for any surgeon. The surgical indications for nasal reconstruction after oncologic resection, trauma or as part of cosmetic rhinoplasty, are steadily increasing. The current attitude for reconstruction is the use of autologous cartilage grafts of various origins (septal, ear or rib) trying to restore a physiological anatomy but their quantity is limited. Thus, in order to produce an implantable cartilaginous model, we developed a study protocol involving human nasal chondrocytes, growth factors and a composite biomaterial and studied at the molecular, cellular and tissue level the phenotype of the chondrocytes cultured in this model.

Materials and methods

After extraction of chondrocytes and their amplification on plastic, the cells were cultured for 15 days either in monolayer or within an agarose hydrogel or a composite biomaterial (agarose/high density polyethylene: Medpor®) in the presence or not of a cocktail of soluble factors (BIT): bone morphogenetic protein-2 (BMP-2), insulin and triiodothyronine (T3). The quality of the chondrocyte phenotype was analyzed by PCR, western blotting and immunohistochemistry.

Results

During their amplification in monolayer, chondrocytes dedifferentiate. However, our results show that the BIT cocktail induces redifferentiation of chondrocytes cultured in agarose/Medpor with synthesis of mature chondrogenic markers. Thereby, chondrocytes associated with the agarose hydrogel will colonize Medpor and synthesize an extracellular matrix characteristic of nasal cartilage.

Conclusion

This nasal cartilage tissue engineering protocol provides the first interesting results for nasal reconstruction.

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以高密度聚乙烯和水凝胶为基础的组织工程鼻软骨重建
研究目的鼻重建对任何外科医生来说都是一个挑战。肿瘤切除、外伤或作为鼻整形术的一部分后鼻部重建的手术指征正在稳步增加。目前对重建的态度是使用各种来源的自体软骨移植物(鼻中隔、耳部或肋骨)试图恢复生理解剖,但数量有限。因此,为了制造可植入软骨模型,我们制定了一项涉及人鼻软骨细胞、生长因子和复合生物材料的研究方案,并在分子、细胞和组织水平上研究了该模型中培养的软骨细胞的表型。材料和方法提取软骨细胞并在塑料上扩增后,细胞在单层或琼脂糖水凝胶或复合生物材料(琼脂糖/高密度聚乙烯:Medpor®)中培养15天,其中存在或不存在可溶性因子(BIT)的混合物:骨形态发生蛋白-2 (BMP-2),胰岛素和三碘甲状腺原氨酸(T3)。采用PCR、western blotting和免疫组织化学分析软骨细胞表型质量。结果软骨细胞在单层扩增过程中发生脱分化。然而,我们的研究结果表明,BIT鸡尾酒诱导琼脂糖/Medpor中培养的软骨细胞再分化,并合成成熟的软骨生成标志物。因此,与琼脂糖水凝胶相关的软骨细胞将定植在Medpor上并合成具有鼻软骨特征的细胞外基质。结论该鼻软骨组织工程方案为鼻重建提供了第一个有趣的结果。
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来源期刊
Pathologie-biologie
Pathologie-biologie 医学-病理学
自引率
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0
审稿时长
6-12 weeks
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