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Modeling Vascularized Bone Regeneration Within a Porous Biodegradable CaP Scaffold Loaded with Growth Factors

机译:在多孔的可生物降解的CaP支架中加载生长因子的血管骨骼再生建模。

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摘要

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.
机译:成骨微环境是一种复杂的构造,其中细胞外基质(ECM)分子,干细胞和生长因子各自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,血管生成的改善和血运重建对成骨至关重要。在这项研究中,我们开发了三维(3D)多尺度系统模型,以研究细胞对从3D可生物降解的多孔磷酸钙(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,并检查了孔径和孔隙率对骨形成和血管生成的影响。结果表明,与孔隙大小相比,支架孔隙率在影响骨骼形成和血管生成方面起着更主要的作用,而可以控制孔隙大小以调整生长因子的释放速率和释放比例。此外,从多层支架释放的梯度VEGF与BMP2和Wnt的组合比单一生长因子更容易促进血管生成和骨形成。这些结果表明,所开发的模型可以潜在地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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