...
首页> 外文期刊>Biomedical materials >Fabrication of polycaprolactone collagen hydrogel constructs seeded with mesenchymal stem cells for bone regeneration
【24h】

Fabrication of polycaprolactone collagen hydrogel constructs seeded with mesenchymal stem cells for bone regeneration

机译:骨髓间充质干细胞接种的聚己内酯胶原水凝胶构建体的制备

获取原文
获取原文并翻译 | 示例
           

摘要

The osteogenic differentiation of bone marrow-derived human mesenchymal stem cells (MSCs) in a collagen I hydrogel was investigated. Collagen hydrogels with 7.5 x 10(5) MSCs ml(-1) were fabricated and cultured for 6 weeks in a defined, osteogenic differentiation medium. Histochemistry revealed morphologically distinct, chondrocyte-like cells, surrounded by a sulfated proteoglycan-rich extracellular matrix in the group treated with bone morphogenetic protein 2 (BMP-2), while cells cultured with dexamethasone, ascorbate-2-phosphate, and beta-glycerophosphate displayed a spindle-shaped morphology and deposited a mineralized matrix. Real-time polymerase chain reaction (RT-PCR) analyses revealed a specific chondrogenic differentiation with the expression of cartilage-specific markers in the BMP-2-treated group and a distinct expression pattern of the osteogenic markers alkaline phosphatase (ALP), type I collagen, osteocalcin (OC), and cbfa-1 in the group treated with an osteogenic standard medium. The collagen gels were used to engineer a cell laden medical grade epsilon-polycaprolactone (PCL)-hydrogel construct for segmental bone repair showing good bonding at the scaffold hydrogel interface and even cell distribution. The results show that MSCs cultured in a collagen I hydrogel are able to undergo a distinct osteogenic differentiation pathway when stimulated with specific differentiation factors and suggest that collagen I hydrogels are a suitable means to facilitate cell seeding of scaffolds for bone tissue engineering applications.
机译:研究了胶原I水凝胶中骨髓来源的人间充质干细胞(MSC)的成骨分化。制造具有7.5 x 10(5)MSCs ml(-1)的胶原蛋白水凝胶,并在确定的成骨分化培养基中培养6周。组织化学显示,在用骨形态发生蛋白2(BMP-2)处理的组中,形态学上明显的软骨细胞样细胞被富含硫酸化蛋白聚糖的细胞外基质包围,而在地塞米松,抗坏血酸-2-磷酸和β-甘油磷酸酯培养的细胞中呈现纺锤形形态并沉积矿化基质。实时聚合酶链反应(RT-PCR)分析显示BMP-2处理组具有软骨特异性标记物表达的特定软骨形成分化和I型成骨标记碱性磷酸酶(ALP)的独特表达模式用成骨标准培养基治疗的组中的胶原蛋白,骨钙素(OC)和cbfa-1。胶原蛋白凝胶被用于工程化载有细胞的医学级ε-聚己内酯(PCL)-水凝胶构建体,用于节段性骨修复,在支架水凝胶界面处显示出良好的结合力,甚至细胞分布均匀。结果表明,当用特异性分化因子刺激时,胶原I水凝胶中培养的MSC能够经历独特的成骨分化途径,并表明胶原I水凝胶是促进支架细胞播种以进行骨组织工程应用的合适方法。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

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