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在加载生长因子的多孔可生物降解 CaP 支架内模拟血管化骨再生。

Modeling vascularized bone regeneration within a porous biodegradable CaP scaffold loaded with growth factors.

机构信息

School of Mathematical Science, Beijing Normal University, Beijing 100875, PR China.

出版信息

Biomaterials. 2013 Jul;34(21):4971-81. doi: 10.1016/j.biomaterials.2013.03.015. Epub 2013 Apr 6.

Abstract

Osteogenetic microenvironment is a complex constitution in which extracellular matrix (ECM) molecules, stem cells and growth factors each interact to direct the coordinate regulation of bone tissue development. Importantly, angiogenesis improvement and revascularization are critical for osteogenesis during bone tissue regeneration processes. In this study, we developed a three-dimensional (3D) multi-scale system model to study cell response to growth factors released from a 3D biodegradable porous calcium phosphate (CaP) scaffold. Our model reconstructed the 3D bone regeneration system and examined the effects of pore size and porosity on bone formation and angiogenesis. The results suggested that scaffold porosity played a more dominant role in affecting bone formation and angiogenesis compared with pore size, while the pore size could be controlled to tailor the growth factor release rate and release fraction. Furthermore, a combination of gradient VEGF with BMP2 and Wnt released from the multi-layer scaffold promoted angiogenesis and bone formation more readily than single growth factors. These results demonstrated that the developed model can be potentially applied to predict vascularized bone regeneration with specific scaffold and growth factors.

摘要

成骨微环境是一个复杂的构成,其中细胞外基质(ECM)分子、干细胞和生长因子相互作用,以指导骨组织发育的协调调节。重要的是,在骨组织再生过程中,血管生成的改善和再血管化对于成骨至关重要。在本研究中,我们开发了一个三维(3D)多尺度系统模型,以研究细胞对从 3D 可生物降解多孔磷酸钙(CaP)支架释放的生长因子的反应。我们的模型重建了 3D 骨再生系统,并研究了孔径和孔隙率对骨形成和血管生成的影响。结果表明,与孔径相比,支架孔隙率在影响骨形成和血管生成方面起着更主导的作用,而孔径可以控制以调整生长因子的释放率和释放分数。此外,梯度 VEGF 与 BMP2 和 Wnt 从多层支架中释放出来,比单一生长因子更能促进血管生成和骨形成。这些结果表明,所开发的模型可潜在地应用于预测具有特定支架和生长因子的血管化骨再生。

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