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采用格子模型方法模拟 CaP 支架在压缩应变下的血管生成和细胞分化。

Simulation of angiogenesis and cell differentiation in a CaP scaffold subjected to compressive strains using a lattice modeling approach.

机构信息

Biomechanics and Mechanobiology, Institute for Bioengineering of Catalonia, C\ Baldiri Reixac, 4, Barcelona 08028, Spain.

出版信息

Biomaterials. 2010 Mar;31(8):2446-52. doi: 10.1016/j.biomaterials.2009.11.063. Epub 2009 Dec 6.

Abstract

Mechanical stimuli are one of the factors that influence tissue differentiation. In the development of biomaterials for bone tissue engineering, mechanical stimuli and formation of a vascular network that transport oxygen to cells within the pores of the scaffolds are essential. Angiogenesis and cell differentiation have been simulated in scaffolds of regular porosity; however, the dynamics of differentiation can be different when the porosity is not uniform. The objective of this study was to investigate the effect of the mechanical stimuli and the capillary network formation on cell differentiation within a scaffold of irregular morphology. A porous scaffold of calcium phosphate based glass was used. The pores and the solid phase were discretized using micro computed tomography images. Cell activity was simulated within the interconnected pore domain of the scaffold using a lattice modeling approach. Compressive strains of 0.5 and 1% of total deformation were applied and two cases of mesenchymal stem cells initialization (in vitro seeding and in vivo) were simulated. Similar capillary networks were formed independently of the cell initialization mode and the magnitude of the mechanical strain applied. Most of vessels grew in the pores at the periphery of the scaffolds and were blocked by the walls of the scaffold. When 0.5% of strain was applied, 70% of the pore volume was affected by mechano-regulatory stimuli corresponding to bone formation; however, because of the lack of oxygen, only 40% of the volume was filled with osteoblasts. 40% of volume was filled with chondrocytes and 3% with fibroblasts. When the mechanical strain was increased to 1%, 11% of the pore volume was filled with osteoblasts, 59% with chondrocytes, and 8% with fibroblasts. This study has shown the dynamics of the correlation between mechanical load, angiogenesis and tissue differentiation within a scaffold with irregular morphology.

摘要

力学刺激是影响组织分化的因素之一。在骨组织工程生物材料的发展中,力学刺激和形成运输氧气到支架孔内细胞的血管网络是必不可少的。在具有规则孔隙率的支架中已经模拟了血管生成和细胞分化;然而,当孔隙率不均匀时,分化的动力学可能会有所不同。本研究的目的是研究力学刺激和毛细血管网络形成对支架中不规则形态细胞分化的影响。使用基于磷酸钙的玻璃多孔支架。使用微计算机断层扫描图像对孔和固相进行离散化。使用格子建模方法模拟支架互连孔域内的细胞活性。施加总变形的 0.5%和 1%的压缩应变,并模拟间充质干细胞初始化(体外接种和体内)的两种情况。无论细胞初始化模式和施加的力学应变大小如何,相似的毛细血管网络都会独立形成。大多数血管在支架边缘的孔中生长,并被支架壁阻塞。当施加 0.5%的应变时,受机械调节刺激影响的孔体积的 70%对应于骨形成;然而,由于缺氧,只有 40%的体积充满成骨细胞。40%的体积充满软骨细胞,3%的体积充满成纤维细胞。当机械应变增加到 1%时,11%的孔体积充满成骨细胞,59%的孔体积充满软骨细胞,8%的孔体积充满成纤维细胞。本研究表明了具有不规则形态支架中力学负载、血管生成和组织分化之间相关性的动力学。

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