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A porous scaffold for bone tissue engineering/45S5 Bioglass~? derived porous scaffolds for co-culturing osteoblasts and endothelial cells

机译:用于骨组织工程的多孔支架/ 45S5 Bioglass〜?衍生的多孔支架,用于共培养成骨细胞和内皮细胞

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摘要

One of the major factors in the therapeutic success of bone tissue engineered scaffolds is the ability of the construct to vascularise post implantation. One of the approaches for improving vascularisation within scaffolds has been to co-culture human umbilical vein endothelial cells (HUVECS) with human osteoblasts (HOBS), which may then promote vascularisation and facilitate tissue regeneration. However, in order to mimic a natural physiological niche it is vital that the scaffold is able to support and promote the proliferation of both cell types and thus become a viable tissue engineered construct. In this study we report the development of a porous bioactive glass-ceramic construct and examine the interaction with human umbilical vein endothelial cells (HUVEC's) and human osteoblast-like cell both in mono and co-culture. The study clearly demonstrated that the scaffolds were able to support both endothelial and human osteoblast cell proliferation both in mono and co-culture. A comparison of the proliferation response of HUVEC and HOB in mono-culture on the test scaffolds and the commercial porous hydroxyapa-tite was assessed over a 28 day period (4, 7, 14, 21 and 28 days), using alamar Blue? assay. Proliferation of HOB cells seeded in the scaffolds was consistently shown to be above those observed on commercial HA scaffolds.
机译:骨组织工程支架治疗成功的主要因素之一是植入后血管生成血管的能力。改善支架内血管化的方法之一是将人脐静脉内皮细胞(HUVECS)与人成骨细胞(HOBS)共培养,然后可促进血管化并促进组织再生。然而,为了模仿天然的生理生态位,至关重要的是,支架能够支持和促进两种细胞类型的增殖,从而成为可行的组织工程构建体。在这项研究中,我们报告了多孔生物活性玻璃陶瓷构造的发展,并研究了在单培养和共培养中与人脐静脉内皮细胞(HUVEC's)和人成骨样细胞的相互作用。该研究清楚地表明,该支架能够在单培养和共培养中支持内皮细胞和人成骨细胞的增殖。在28天内(4、7、14、21和28天),使用alamar Blue?评估了HUVEC和HOB在测试支架和市售多孔羟基磷灰石上单培养的增殖反应的比较。分析。始终显示出植入支架中的HOB细胞的增殖高于在商业HA支架上观察到的增殖。

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    《Journal of materials science》 |2010年第3期|p.893-905|共13页
  • 作者单位

    Department of Biomaterials, Biomimetics and Biophotonics, King's College London Dental Institute, Floor 17, Tower Wing, Guy's Hospital, London Bridge, SE1 9RT London, UK;

    rnDepartment of Biomaterials, Biomimetics and Biophotonics, King's College London Dental Institute, Floor 17, Tower Wing, Guy's Hospital, London Bridge, SE1 9RT London, UK;

    rnDepartment of Biomaterials, Biomimetics and Biophotonics, King's College London Dental Institute, Floor 17, Tower Wing, Guy's Hospital, London Bridge, SE1 9RT London, UK;

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