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富血小板血浆和脂肪组织来源的微血管片段的生物学涂层可改善多孔聚乙烯的血管化、生物相容性和组织整合。

Biological coating with platelet-rich plasma and adipose tissue-derived microvascular fragments improves the vascularization, biocompatibility and tissue incorporation of porous polyethylene.

机构信息

Institute for Clinical and Experimental Surgery, Saarland University, 66421 Homburg/Saar, Germany.

Institute for Clinical and Experimental Surgery, Saarland University, 66421 Homburg/Saar, Germany; Department of Trauma, Hand and Reconstructive Surgery, Saarland University, 66421 Homburg/Saar, Germany.

出版信息

Acta Biomater. 2020 May;108:194-206. doi: 10.1016/j.actbio.2020.03.018. Epub 2020 Mar 17.

Abstract

Porous polyethylene (pPE) is a commonly used biomaterial in craniofacial reconstructive surgery. However, implant failure due to insufficient vascularization represents a major issue. To overcome this problem, we herein introduce an effective strategy to improve the vascularization and incorporation of pPE. Adipose tissue-derived microvascular fragments (MVF) from transgenic green fluorescent protein (GFP) mice were suspended in platelet-rich plasma (PRP) for the coating of pPE. PRP/MVF-coated pPE as well as PRP-coated and uncoated controls were subsequently implanted into the dorsal skinfold chamber and the flanks of GFP wild-type mice to analyze their in vivo performance throughout 2, 4 and 8 weeks by means of intravital fluorescence microscopy, histology and immunohistochemistry. The GFP/GFP cross-over design allowed the identification of GFP MVF within the implants. Shortly after implantation, they rapidly reassembled into new blood-perfused microvascular networks, resulting in a significantly accelerated vascularization of PRP/MVF-coated pPE when compared to both controls. The overall numbers of rolling and adherent leukocytes within the microcirculation as well as macrophages, multi-nucleated giant cells and mast cells around the implants did not differ between the three groups. However, in contrast to uncoated controls, PRP/MVF-coated and PRP-coated pPE promoted pro-angiogenic M2 macrophage polarization at the implantation site. These findings demonstrate that PRP/MVF-coating represents a highly effective strategy to enhance the vascularization, biocompatibility and tissue incorporation of pPE. STATEMENT OF SIGNIFICANCE: The clinical in vivo performance of implanted biomaterials is crucially dependent on their adequate incorporation into the body. To achieve this, we herein introduce an effective biological coating strategy. Our results demonstrate that coating with PRP and MVF accelerates and enhances the vascularization, biocompatibility and tissue incorporation of porous polyethylene. Because this type of biological coating is easily applicable on any type of biomaterial, our approach may rapidly be translated into clinical practice to improve the outcome of various regenerative approaches.

摘要

多孔聚乙烯(pPE)是颅颌面重建外科中常用的生物材料。然而,由于血管化不足导致的植入物失败是一个主要问题。为了克服这个问题,我们在此引入了一种有效策略来改善 pPE 的血管化和整合。从转绿色荧光蛋白(GFP)小鼠的脂肪组织中提取的微血管片段(MVF)悬浮在富含血小板的血浆(PRP)中,用于涂覆 pPE。随后将 PRP/MVF 涂覆的 pPE 以及 PRP 涂覆和未涂覆的对照物植入 GFP 野生型小鼠的背部皮褶室和侧腹,通过活体荧光显微镜、组织学和免疫组织化学分析它们在 2、4 和 8 周内的体内性能。GFP/GFP 交叉设计允许鉴定植入物内的 GFP-MVF。植入后不久,它们迅速重新组装成新的血流灌注微血管网络,与对照组相比,PRP/MVF 涂覆的 pPE 的血管化速度明显加快。微血管内滚动和黏附的白细胞以及植入物周围的巨噬细胞、多核巨细胞和肥大细胞的总数在三组之间没有差异。然而,与未涂覆的对照物相比,PRP/MVF 涂覆的和 PRP 涂覆的 pPE 在植入部位促进了促血管生成的 M2 巨噬细胞极化。这些发现表明,PRP/MVF 涂层是一种增强 pPE 血管化、生物相容性和组织整合的有效策略。

声明的意义

植入生物材料的临床体内性能主要取决于其在体内的充分整合。为了实现这一目标,我们在此引入了一种有效的生物涂层策略。我们的结果表明,用 PRP 和 MVF 涂覆可以加速和增强多孔聚乙烯的血管化、生物相容性和组织整合。由于这种类型的生物涂层很容易适用于任何类型的生物材料,我们的方法可能会迅速转化为临床实践,以提高各种再生方法的效果。

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