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用复合支架构建工程耳结构以维持其尺寸。

Engineering ear constructs with a composite scaffold to maintain dimensions.

机构信息

Department of Surgery, Massachusetts General Hospital, Boston, Massachusetts 02114, USA.

出版信息

Tissue Eng Part A. 2011 Jun;17(11-12):1573-81. doi: 10.1089/ten.TEA.2010.0627. Epub 2011 Mar 13.

DOI:10.1089/ten.TEA.2010.0627
PMID:21284558
Abstract

Engineered cartilage composed of a patient's own cells can become a feasible option for auricular reconstruction. However, distortion and shrinkage of ear-shaped constructs during scaffold degradation and neocartilage maturation in vivo have hindered the field. Scaffolds made of synthetic polymers often generate degradation products that cause an inflammatory reaction and negatively affect neocartilage formation in vivo. Porous collagen, a natural material, is a promising candidate; however, it cannot withstand the contractile forces exerted by skin and surrounding tissue during normal wound healing. We hypothesised that a permanent support in the form of a coiled wire embedded into a porous collagen scaffold will maintain the construct's size and ear-specific shape. Half-sized human adult ear-shaped fibrous collagen scaffolds with and without embedded coiled titanium wire were seeded with sheep auricular chondrocytes, cultured in vitro for up to 2 weeks, and implanted subcutaneously on the backs of nude mice. After 6 weeks, the dimensional changes in all implants with wire support were minimal (2.0% in length and 4.1% in width), whereas significant reduction in size occurred in the constructs without embedded wire (14.4% in length and 16.5% in width). No gross distortion occurred over the in vivo study period. There were no adverse effects on neocartilage formation from the embedded wire. Histologically, mature neocartilage extracellular matrix was observed throughout all implants. The amount of DNA, glycosaminoglycan, and hydroxyproline in the engineered cartilage were similar to that of native sheep ear cartilage. The embedded wire support was essential for avoiding shrinkage of the ear-shaped porous collagen constructs.

摘要

由患者自身细胞构成的工程化软骨可为耳廓重建提供一种可行的选择。然而,在体内支架降解和新生软骨成熟过程中,耳形构建体的变形和收缩一直阻碍着该领域的发展。由合成聚合物制成的支架通常会产生降解产物,引起炎症反应,并对体内新生软骨的形成产生负面影响。多孔胶原作为一种天然材料是一种很有前途的候选材料,但它无法承受正常伤口愈合过程中皮肤和周围组织产生的收缩力。我们假设,以嵌入式螺旋线的形式存在的永久性支撑物将维持构建体的大小和耳特异性形状。带有和不带有嵌入式螺旋钛丝的半尺寸成人耳状纤维胶原支架被绵羊耳廓软骨细胞接种,在体外培养长达 2 周,并植入裸鼠背部的皮下。6 周后,所有带有线材支撑的植入物的尺寸变化都很小(长度变化 2.0%,宽度变化 4.1%),而没有嵌入式线材的构建体的尺寸显著减小(长度变化 14.4%,宽度变化 16.5%)。在体内研究期间,没有发生明显的变形。嵌入式线材对新生软骨的形成没有不良影响。组织学上,所有植入物中均观察到成熟的新生软骨细胞外基质。工程化软骨中的 DNA、糖胺聚糖和羟脯氨酸含量与天然绵羊耳软骨相似。嵌入式线材支撑对于避免耳状多孔胶原构建体的收缩是必不可少的。

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