首页> 外文期刊>Osteoarthritis and cartilage >Scaffold degradation elevates the collagen content and dynamic compressive modulus in engineered articular cartilage.
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Scaffold degradation elevates the collagen content and dynamic compressive modulus in engineered articular cartilage.

机译:支架降解提高了工程性关节软骨中的胶原蛋白含量和动态压缩模量。

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OBJECTIVE: It was hypothesized that controlled, scaffold removal in engineered cartilage constructs would improve their collagen content and mechanical properties over time in culture. DESIGN: Preliminary experiments characterized the effects of agarase on cell-free agarose disks and cartilage explants. Immature bovine chondrocytes were encapsulated in agarose, cultured to day 42, and incubated with 100 units/mL agarase for 48 h. After treatment, constructs were cultured to day 91. The compressive Young's modulus and dynamic modulus of the constructs were determined every 2 weeks and immediately after agarase treatment. Post-mechanical testing, constructs were processed for biochemistry and histology. RESULTS: Agarase treatment on explants had no detrimental effect on the cartilage matrix. Treatment applied to engineered constructs on day 42 did not affect DNA or collagen content. Agarase treatment decreased tissue GAG content (via GAG loss to the media) and Young's modulus, both of which recovered to control values over time in culture. By day 91 agarase-treated constructs possessed approximately 25% more DNA, approximately 60% more collagen, and approximately 40% higher dynamic modulus compared to untreated controls. CONCLUSIONS: Scaffold degradation increased construct collagen content and dynamic mechanical properties, affirming the experimental hypothesis. The mechanism may lie in increased nutrient transport, increased space for collagen fibril formation, and cellular response to the loss of GAG with agarase treatment. The results highlight the role of the scaffold in retaining synthesized matrix during early and late tissue formation. This work also shows promise in developing an engineered tissue that may be completely free of scaffold material for clinical implantation.
机译:目的:假设在工程化的软骨构建体中进行有控制的支架去除会随着时间的流逝改善其胶原蛋白含量和机械性能。设计:初步实验表征了琼脂酶对无细胞琼脂糖盘和软骨外植体的影响。将未成熟的牛软骨细胞封装在琼脂糖中,培养至第42天,并与100单位/ mL的琼脂酶孵育48小时。处理后,将构建体培养至第91天。每两周一次并在琼脂酶处理后立即测定该构建体的压缩杨氏模量和动态模量。机械后测试,对构建体进行了生物化学和组织学处理。结果:琼脂糖酶处理外植体对软骨基质无不利影响。在第42天对工程构建体进行的处理不影响DNA或胶原含量。琼脂糖酶处理降低了组织GAG含量(通过GAG损失到培养基中)和杨氏模量,两者在培养中随时间恢复到控制值。到第91天,与未处理的对照相比,用琼脂糖酶处理的构建体拥有大约25%的DNA,大约60%的胶原蛋白和大约40%的动态模量。结论:支架降解增加了结构胶原含量和动态力学性能,证实了实验假设。其机制可能在于养分转运增加,胶原蛋白原纤维形成的空间增加以及琼脂酶处理导致细胞对GAG丧失的反应。结果突出了支架在早期和晚期组织形成过程中保留合成基质的作用。这项工作还显示出开发出一种工程组织的希望,该组织可能完全不含用于临床植入的支架材料。

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