首页> 美国卫生研究院文献>other >Approaching the Compressive Modulus of Articular Cartilage With a Decellularized Cartilage-Based Hydrogel
【2h】

Approaching the Compressive Modulus of Articular Cartilage With a Decellularized Cartilage-Based Hydrogel

机译:基于脱细胞软骨的水凝胶处理关节软骨的压缩模量

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

ECM-based materials are appealing for tissue engineering strategies because they may promote stem cell recruitment, cell infiltration, and cell differentiation without the need to supplement with additional biological factors. Cartilage ECM has recently shown potential to be chondroinductive, particularly in a hydrogel-based system, which may be revolutionary in orthopedic medicine. However, hydrogels composed of natural materials are often mechanically inferior to synthetic materials, which is a major limitation for load-bearing tissue applications. The objective was therefore to create an unprecedented hydrogel derived entirely from native cartilage ECM that was both mechanically more similar to native cartilage tissue and capable of inducing chondrogenesis. Porcine cartilage was decellularized, solubilized, and then methacrylated and UV photocrosslinked to create methacrylated solubilized decellularized cartilage (MeSDCC) gels. Methacrylated gelatin (GelMA) was employed as a control for both biomechanics and bioactivity. Rat bone marrow-derived mesenchymal stem cells were encapsulated in these networks, which were cultured in vitro for 6 weeks, where chondrogenic gene expression, the compressive modulus, swelling, and histology were analyzed. One day after crosslinking, the elastic compressive modulus of the 20% MeSDCC gels was 1070 ± 150 kPa. Most notably, the stress strain profile of the 20% MeSDCC gels fell within the 95% confidence interval range of native porcine cartilage. Additionally, MeSDCC gels significantly upregulated chondrogenic genes compared to GelMA as early as day 1 and supported extensive matrix synthesis as observed histologically. Given that these gels approached the mechanics of native cartilage tissue, supported matrix synthesis, and induced chondrogenic gene expression, MeSDCC hydrogels may be promising materials for cartilage tissue engineering applications. Future efforts will focus on improving fracture mechanics as well to benefit overall biomechanical performance.
机译:基于ECM的材料吸引组织工程策略,因为它们可以促进干细胞募集,细胞浸润和细胞分化,而无需补充其他生物因子。软骨ECM最近已显示出潜在的软骨诱导性,特别是在基于水凝胶的系统中,这在骨科医学中可能是革命性的。然而,由天然材料组成的水凝胶在机械上通常不如合成材料,这是承重组织应用的主要限制。因此,目的是创造一种空前的水凝胶,其完全源自天然软骨ECM,其在机械上与天然软骨组织更相似,并且能够诱导软骨形成。将猪软骨脱细胞,溶解,然后进行甲基丙烯酸酯化和UV光交联,以生成甲基丙烯酸酯化的可溶性脱细胞软骨(MeSDCC)凝胶。甲基丙烯酸明胶(GelMA)被用作生物力学和生物活性的对照。将大鼠骨髓来源的间充质干细胞封装在这些网络中,在体外培养6周,然后分析软骨生成基因的表达,压缩模量,肿胀和组织学。交联后一天,20%MeSDCC凝胶的弹性压缩模量为1070±150 kPa。最值得注意的是,20%MeSDCC凝胶的应力应变曲线落在天然猪软骨的95%置信区间范围内。此外,与GelMA相比,MeSDCC凝胶最早在第1天就显着上调了软骨形成基因,并且如组织学观察到的,支持广泛的基质合成。鉴于这些凝胶接近天然软骨组织的力学,支持基质合成以及诱导软骨形成基因表达,MeSDCC水凝胶可能是用于软骨组织工程应用的有前途的材料。未来的工作将集中在改善断裂力学上,以提高整体生物力学性能。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号