National Engineering Research Center for Biomaterials, Sichuan University, Chengdu 610064, PR China.
Engineering Research Center in Biomaterials, Sichuan University, Chengdu 610064, PR China.
ACS Biomater Sci Eng. 2020 Jun 8;6(6):3275-3286. doi: 10.1021/acsbiomaterials.9b01841. Epub 2020 May 8.
The understanding of the mineralization of collagen for bone formation is a current key theme in bone tissue engineering and is of great relevance to the fabrication of novel biomimetic bone grafting materials. The noncollagenous proteins (NCPs) play a vital role in bone formation and are considered to be responsible for regulating intrafibrillar penetration of minerals into collagen fibrils by means of their abundant polyanionic domains. In this study, alginate, as a NCPs analogue, was introduced in the mineralization of collagen to mediate the collagen self-assembly with simultaneous hydroxyapatite (HA) synthesis. The biomimetic systems were based upon the self-assembly of collagen (Col) or collagen-alginate (CA) in the absence or presence of a varying content of HA. The alginate-mediated effects were found to include the lateral aggregation of small fibrils into the extremely large bundles and the assisted deposition of HA for a larger mineralized fibril. This alginate-assisted mineralization of collagen gave rise to an exquisite 3D mineralized architecture with enhanced mechanical property. The cell viability experiments showed the excellent proliferation and spreading morphologies of rat bone mesenchymal stem cells (MSCs) on the assembled products, and a higher expression of osteogenic differentiation related transcription factor was obtained in the alginate-assisted mineralization of collagen. This study indicated that the selection of an appropriate substance, e.g., alginate as an anionic polyelectrolyte with Ca-capturing property, could be a convenient, simple solution to achieve a mineralized collagen scaffold with the reinforced mechanical property for potential applications in bone regeneration.
胶原矿化对于骨形成的理解是骨组织工程学当前的一个关键主题,对于新型仿生骨移植物材料的制备具有重要意义。非胶原蛋白(NCPs)在骨形成中起着至关重要的作用,被认为通过其丰富的多阴离子结构域负责调节矿物质在胶原原纤维内的渗透。在这项研究中,海藻酸钠作为 NCPs 的类似物,被引入到胶原的矿化中,以介导胶原的自组装和同时合成羟基磷灰石(HA)。仿生系统基于无或有变化含量的 HA 存在下胶原(Col)或胶原-海藻酸钠(CA)的自组装。发现海藻酸钠介导的作用包括小原纤维的侧向聚集形成非常大的束和 HA 的辅助沉积形成更大的矿化原纤维。这种海藻酸钠辅助的胶原矿化导致了具有增强机械性能的精致的 3D 矿化结构。细胞活力实验表明,大鼠骨髓间充质干细胞(MSCs)在组装产物上具有良好的增殖和扩展形态,并且在胶原的海藻酸钠辅助矿化中获得了更高的成骨分化相关转录因子的表达。这项研究表明,选择合适的物质,例如具有 Ca 捕获能力的阴离子聚电解质海藻酸钠,可以作为一种方便、简单的解决方案,实现具有增强机械性能的矿化胶原支架,用于潜在的骨再生应用。