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Enhancing cell seeding and osteogenesis of MSCs on 3D printed scaffolds through injectable BMP2 immobilized ECM-Mimetic gel

机译:通过注射BMP2固定的ECM - 模拟凝胶,增强3D印刷支架上MSCs的细胞播种和骨质发生

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Objective. Design of bioactive scaffolds with osteogenic capacity is a central challenge in cell-based patient-specific bone tissue engineering. Efficient and spatially uniform seeding of (stem) cells onto such constructs is vital to attain functional tissues. Herein we developed heparin functionalized collagen gels supported by 3D printed bioceramic scaffolds, as bone extracellular matrix (ECM)-mimetic matrices. These matrices were designed to enhance cell seeding efficiency of mesenchymal stem cells (MSCs) as well as improve their osteogenic differentiation through immobilized bone morphogenic protein 2 (BMP2) to be used for personalized bone regeneration.Methods. A 3D gel based on heparin-conjugated collagen matrix capable of immobilizing recombinant human bone morphogenic protein 2 (BMP2) was synthesized. Isolated dental pulp Mesenchymal stem cells (MSCs) were then encapsulated into the bone ECM microenvironment to efficiently and uniformly seed a bioactive ceramic-based scaffold fabricated using additive manufacturing technique. The designed 3D cell-laden constructs were comprehensively investigated trough in vitro assays and in vivo study.Results. In-depth rheological characterizations of heparin-conjugated collagen gel revealed that elasticity of the matrix is significantly improved compared with freely incorporated heparin. Investigation of the MSCs laden collagen-heparin hydrogels revealed their capability to provide spatiotemporal bioavailability of BMP2 while suppressing the matrix contraction over time. The in vivo histology and real-time polymerase chain reaction (qPCR) analysis showed that the designed construct supported the osteogenic differentiation of MSCs and induced the ectopic bone formation in rat model.Significance. The presented hybrid constructs combine bone ECM chemical cues with mechanical function providing an ideal 3D microenvironment for patient-specific bone tissue engineering and cell therapy applications. The implemented methodology in design of ECM-mimetic 3D matrix capable of immobilizing BMP2 to improve seeding efficiency of customized scaffolds can be exploited for other bioactive molecules. (C) 2019 The Academy of Dental Materials. Published by Elsevier Inc. All rights reserved.
机译:客观的。具有成骨容量的生物活性支架设计是细胞基患者特异性骨组织工程中的中枢挑战。 (茎)细胞在这些构建体上的高效和空间均匀的播种对于获得功能组织至关重要。在此,我们开发了由3D印刷的生物陶瓷支架支撑的肝素官能化胶原凝胶,作为骨细胞外基质(ECM) - 纤维化基质。这些基质被设计成增强间充质干细胞(MSCs)的细胞播种效率,以及通过固定化的骨形态发生蛋白2(BMP2)来改善其骨质发生分化以用于个性化骨再生。方法。合成了一种基于能够固定重组人骨形态发生蛋白2(BMP2)的肝素缀合的胶原基质的3D凝胶。然后将分离的牙髓间充质干细胞(MSCs)包封在骨ECM微环境中,以有效均匀地种子使用添加剂制造技术制造的生物活性陶瓷基支架。在体外测定和体内研究中,精心研究了设计的3D细胞载体构建体。结果。与自由掺入肝素相比,肝素 - 缀合的胶原凝胶的深度流变特征显示,与自由掺入肝素相比,基质的弹性显着提高。 MSCs Laden胶原蛋白 - 肝素水凝胶的研究揭示了它们在抑制随时间抑制基质收缩的同时提供BMP2的时空生物利用度。体内组织学和实时聚合酶链反应(QPCR)分析表明,设计的构建体支持MSCs的成骨分化并诱导大鼠模型中的异位骨形成。呈现的杂交构建体与机械函数结合骨ECM化学提示,为患者特异性骨组织工程和细胞疗法应用提供理想的3D微环境。能够固定BMP2的ECM模拟3D基质设计中的实施方法,以提高定制支架的种子效率,可以利用其他生物活性分子。 (c)2019年牙科材料学院。由elsevier Inc.出版的所有权利保留。

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