首页> 外文期刊>American Journal of Sports Medicine >Facilitating In Vivo Articular Cartilage Repair by Tissue-Engineered Cartilage Grafts Produced From Auricular Chondrocytes
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Facilitating In Vivo Articular Cartilage Repair by Tissue-Engineered Cartilage Grafts Produced From Auricular Chondrocytes

机译:通过耳廓软骨细胞产生的组织工程化软骨移植物促进体内关节软骨修复

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Background: Insufficient cell numbers still present a challenge for articular cartilage repair. Converting heterotopic auricular chondrocytes by extracellular matrix may be the solution. Hypothesis: Specific extracellular matrix may convert the phenotype of auricular chondrocytes toward articular cartilage for repair. Study Design: Controlled laboratory study. Methods: For in vitro study, rabbit auricular chondrocytes were cultured in monolayer for several passages until reaching status of dedifferentiation. Later, they were transferred to chondrogenic type II collagen (Col II)–coated plates for further cell conversion. Articular chondrogenic profiles, such as glycosaminoglycan deposition, articular chondrogenic gene, and protein expression, were evaluated after 14-day cultivation. Furthermore, 3-dimensional constructs were fabricated using Col II hydrogel-associated auricular chondrocytes, and their histological and biomechanical properties were analyzed. For in vivo study, focal osteochondral defects were created in the rabbit knee joints, and auricular Col II constructs were implanted for repair. Results: The auricular chondrocytes converted by a 2-step protocol expressed specific profiles of chondrogenic molecules associated with articular chondrocytes. The histological and biomechanical features of converted auricular chondrocytes became similar to those of articular chondrocytes when cultivated with Col II 3-dimensional scaffolds. In an in vivo animal model of osteochondral defects, the treated group (auricular Col II) showed better cartilage repair than did the control groups (sham, auricular cells, and Col II). Histological analyses revealed that cartilage repair was achieved in the treated groups with abundant type II collagen and glycosaminoglycans syntheses rather than elastin expression. Conclusion: The study confirmed the feasibility of applying heterotopic chondrocytes for cartilage repair via extracellular matrix–induced cell conversion. Clinical Relevance: This study proposes a feasible methodology to convert heterotopic auricular chondrocytes for articular cartilage repair, which may serve as potential alternative sources for cartilage repair.
机译:背景:细胞数量不足仍然为关节软骨修复呈现挑战。通过细胞外基质转换异位耳廓软骨细胞可以是溶液。假设:特异性细胞外基质可以将耳廓软骨细胞的表型转化为关节软骨进行修复。研究设计:受控实验室研究。方法:对于体外研究,兔耳廓软骨细胞在单层培养,若干通道直至达到去除湿的状态。后来,它们被转移到软骨型II型胶原(COL II)涂层的平板中,用于进一步细胞转化。在14天的培养后,评估关节性软骨型,例如糖胺聚糖沉积,关节软骨基因和蛋白质表达。此外,使用COL II水凝胶相关的耳细胞制造3维构建体,分析了它们的组织学和生物力学性质。对于在体内研究中,在兔膝关节中产生焦体骨质缺陷,植入耳廓COL II构建体进行修复。结果:由2步方案转化的耳廓软骨细胞表达了与关节软骨细胞相关的软骨内分子的特异性曲线。随着COL II三维支架培养时,转化的耳廓软骨细胞的组织学和生物力学特征与关节软骨细胞相似。在体内动物模型中的骨质色神节缺损,治疗组(耳廓COL II)显示出比对照组(假,耳廓细胞和COL II)更好的软骨修复。组织学分析表明,用丰富的II型胶原蛋白和糖胺聚糖合成而不是Elastin表达,在处理的基团中实现了软骨修复。结论:该研究证实了通过细胞外基质诱导的细胞转化施用包裹物型软骨细胞的可行性。临床相关性:本研究提出了一种可行的方法,用于转换外观耳廓软骨细胞用于关节软骨修复,这可以作为软骨修复的潜在替代来源。

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