Institute of Crystallography - CNR, via Salaria Km 29.300, 00015, Monterotondo Roma, Italy.
Nanoscale. 2017 Nov 16;9(44):17274-17283. doi: 10.1039/c7nr05013e.
The mineralization process is crucial to the load-bearing characteristics of the bone extracellular matrix. In this work, we have studied the spatiotemporal dynamics of mineral deposition by human bone marrow mesenchymal stem cells differentiating toward osteoblasts promoted by the presence of exogenous hydroxyapatite nanoparticles. At the molecular level, the added nanoparticles positively modulated the expression of bone-specific markers and enhanced calcified matrix deposition during osteogenic differentiation. The nucleation, growth and spatial arrangement of newly deposited hydroxyapatite nanocrystals have been evaluated using scanning micro X-ray diffraction and scanning micro X-ray fluorescence. As leading results, we have found the emergence of a complex scenario where the spatial organization and temporal evolution of the process exhibit heterogeneous and self-organizing dynamics. At the same time the possibility of controlling the differentiation kinetics, through the addition of synthetic nanoparticles, paves the way to empower the generation of more structured bone scaffolds in tissue engineering and to design new drugs in regenerative medicine.
矿化过程对于骨细胞外基质的承载特性至关重要。在这项工作中,我们研究了人骨髓间充质干细胞向成骨细胞分化过程中,外源性羟基磷灰石纳米粒子促进的矿化沉积的时空动力学。在分子水平上,添加的纳米粒子可正向调控骨特异性标志物的表达,并在成骨分化过程中增强矿化基质的沉积。通过扫描微 X 射线衍射和扫描微 X 射线荧光评估了新沉积羟基磷灰石纳米晶体的成核、生长和空间排列。作为主要结果,我们发现出现了一种复杂的情况,其中该过程的空间组织和时间演化表现出异质和自组织动力学。同时,通过添加合成纳米粒子来控制分化动力学的可能性为在组织工程中生成更具结构的骨支架以及为再生医学设计新型药物开辟了道路。