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首页> 外文期刊>Biomaterials >Bone and cartilage tissue constructs grown using human bone marrow stromal cells, silk scaffolds and rotating bioreactors
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Bone and cartilage tissue constructs grown using human bone marrow stromal cells, silk scaffolds and rotating bioreactors

机译:使用人骨髓基质细胞,丝支架和旋转生物反应器生长的骨和软骨组织构建体

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摘要

Human bone marrow contains a population of bone marrow stromal cells (hBMSCs) capable of forming several types of mesenchymal tissues, including bone and cartilage. The present study was designed to test whether large cartilaginous and bone-like tissue constructs can be selectively engineered using the same cell population (hBMSCs), the same scaffold type (porous silk) and same hydrodynamic environment (construct settling in rotating bioreactors), by varying the medium composition (chondrogenic vs. osteogenic differentiation factors): The hBMSCs were harvested, expanded and characterized with respect to their differentiation potential and population distribution. Passage two cells were seeded on scaffolds and cultured for 5 weeks in bioreactors using osteogenic, chondrogenic or control medium. The three media yielded constructs with comparable wet weights and compressive moduli (similar to 25 kPa). Chondrogenic medium yielded constructs with higher amounts of DNA (1.5-fold) and glycosaminoglycans (GAG, 4-fold) per unit wet weight (ww) than control medium. In contrast, osteogenic medium yielded constructs with higher dry weight (1.6-fold), alkaline phosphatase (AP) activity (8-fold) and calcium content (100-fold) per unit ww than control medium. Chondrogenic medium yielded constructs that were weakly positive for GAG by contrast-enhanced MRI and alcian blue stain, whereas osteogenic medium yielded constructs that were highly mineralized by mu CT and von Kossa stain. Engineered bone constructs were large (8 mm diameter x 2 mm thick disks) and resembled trabecular bone with respect to structure and mineralized tissue volume fraction (12%). (c) 2006 Elsevier Ltd. All rights reserved.
机译:人骨髓包含一群能够形成几种类型的间充质组织(包括骨骼和软骨)的骨髓基质细胞(hBMSC)。本研究旨在通过以下方法测试是否可以使用相同的细胞群(hBMSC),相同的支架类型(多孔丝)和相同的流体动力学环境(构建物在旋转生物反应器中沉降)选择性地工程化大型软骨和骨样组织构建物。改变培养基成分(软骨分化与成骨分化因子):收获,扩增和鉴定hBMSCs的分化潜能和种群分布。将传代的两个细胞接种在支架上,并使用成骨,成软骨或对照培养基在生物反应器中培养5周。三种介质产生具有可比的湿重和压缩模量(类似于25 kPa)的构造。软骨形成培养基产生的构建体每单位湿重(ww)具有比对照培养基更高的DNA(1.5倍)和糖胺聚糖(GAG,4倍)数量。相反,与对照培养基相比,成骨培养基产生的干重(1.6倍),碱性磷酸酶(AP)活性(8倍)和钙含量(100倍)更高。通过造影剂增强的MRI和阿尔辛蓝染色,软骨形成培养基产生的GAG阳性呈弱阳性,而成骨培养基产生的μCT和von Kossa染色高度矿化。经过改造的骨骼构造较大(直径8毫米x 2毫米厚的椎间盘),在结构和矿化组织体积分数(12%)方面类似于小梁骨。 (c)2006 Elsevier Ltd.保留所有权利。

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