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用软骨细胞使多孔聚乙烯(Medpor®)活化,可促进早期种植体血管化和与宿主组织结合。

Vitalization of porous polyethylene (Medpor®) with chondrocytes promotes early implant vascularization and incorporation into the host tissue.

机构信息

Institute for Clinical and Experimental Surgery, University of Saarland, Homburg/Saar, Germany.

出版信息

Tissue Eng Part A. 2012 Aug;18(15-16):1562-72. doi: 10.1089/ten.TEA.2011.0340. Epub 2012 Apr 26.

Abstract

Porous polyethylene (Medpor(®)) is frequently used in craniofacial reconstructive surgery. The successful incorporation of this alloplastic biomaterial depends on adequate vascularization. Here, we analyzed whether the early vascularization of porous polyethylene can be accelerated by vitalization with human chondrocytes. For this purpose, small polyethylene samples were coated with platelet-rich plasma (PRP) or a suspension of PRP and human chondrocytes. Uncoated polyethylene samples served as controls. Subsequently, the samples were implanted into the dorsal skinfold chamber of CD-1 nude mice to repetitively analyze their vascularization and biocompatibility by means of intravital fluorescence microscopy. PRP-chondrocyte-coated polyethylene exhibited an accelerated and improved vascularization when compared with the other two groups. This was indicated by a significantly higher functional capillary density of the microvascular network developing around the implants. Moreover, a leukocyte-endothelial cell interaction was found in a physiological range at the implantation site of all three groups, demonstrating that the vitalization with PRP and chondrocytes did not affect the good biocompatibility of the alloplastic material. Additional histological, immunohistochemical, and in situ hybridization analyses revealed that the chondrocytes formed a bioprotective tissue layer, which prevented the accumulation of macrophages and foreign body giant cells on the polyethylene surface. These findings clearly indicate that vitalization of polyethylene with chondrocytes promotes early implant vascularization and incorporation into the host tissue and, thus, may be a promising approach that prevents postoperative complications such as implant extrusion, migration, and infection.

摘要

多孔聚乙烯(Medpor(®))常用于颅面重建手术。这种同种异体生物材料的成功植入依赖于充分的血管化。在这里,我们分析了用人软骨细胞对多孔聚乙烯进行活力化是否可以加速其早期血管化。为此,将小的聚乙烯样本用富含血小板的血浆 (PRP) 或 PRP 和人软骨细胞的混悬液进行涂层处理。未涂层的聚乙烯样本作为对照。随后,将这些样本植入 CD-1 裸鼠的背部皮肤囊腔中,通过活体荧光显微镜重复分析它们的血管化和生物相容性。与其他两组相比,PRP-软骨细胞涂层的聚乙烯表现出加速和改善的血管化。这是由围绕植入物形成的微血管网络的功能毛细血管密度显著增加所表明的。此外,在所有三组的植入部位均发现白细胞-内皮细胞相互作用处于生理范围内,表明 PRP 和软骨细胞的活力化并未影响同种异体材料的良好生物相容性。额外的组织学、免疫组织化学和原位杂交分析表明,软骨细胞形成了生物保护组织层,防止巨噬细胞和异物巨细胞在聚乙烯表面聚集。这些发现清楚地表明,用软骨细胞对聚乙烯进行活力化可以促进早期植入物血管化和与宿主组织的结合,因此可能是一种有前途的方法,可以预防术后并发症,如植入物挤出、迁移和感染。

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