Costa-Rodrigues J, Carmo S, Perpétuo I P, Monteiro F J, Fernandes M H
Laboratory for Bone Metabolism and Regeneration, Faculty of Dental Medicine, University of Porto, Portugal; ESTSP - Escola Superior de Tecnologia da Saúde do Porto, Instituto Politécnico do Porto, Portugal.
Laboratory for Bone Metabolism and Regeneration, Faculty of Dental Medicine, University of Porto, Portugal; Departamento de Engenharia Metalúrgica e de Materiais, Faculdade de Engenharia, Universidade do Porto, Portugal.
Biochim Biophys Acta. 2016 Apr;1860(4):825-35. doi: 10.1016/j.bbagen.2016.01.014. Epub 2016 Jan 19.
Surface topography is a key parameter in bone cells-biomaterials interactions. This study analyzed the behavior of human osteoclast precursor cells cultured over three hydroxyapatite (HA) surfaces ranging from a micro- to nanoscale topography.
HA surfaces were prepared with microsized HA particles, at 1300°C (HA1), and with nanosized HA particles at 1000°C (HA2) and 830°C (HA3). Human osteoclast precursors were cultured in the absence or presence of M-SCF and RANKL.
HA surfaces had similar chemical composition, however, HA1 and HA3 presented typical micro- and nanostructured topographies, respectively, and HA2 profile was between those of HA1 and HA3. The decrease on the average grain diameter to the nanoscale range (HA3) was accompanied by an increase in surface area, porosity and hydrophilicity and a decrease in roughness. Compared to HA1 surface, HA3 allowed a lower osteoclastic adhesion, differentiation and function. Differences in the cell response appeared to be associated with the modulation of relevant intracellular signaling pathways.
The decrease in HA grain size to a biomimetic nanoscale range, appears less attractive to osteoclastic differentiation and function, compared to the HA microsized topography.
This observation emphasizes the role of surface topography in designing advanced biomaterials for tailored bone cells response in regenerative strategies.
表面形貌是骨细胞与生物材料相互作用的关键参数。本研究分析了在三种从微米级到纳米级形貌的羟基磷灰石(HA)表面上培养的人破骨细胞前体细胞的行为。
用微米级HA颗粒在1300°C制备HA表面(HA1),用纳米级HA颗粒在1000°C(HA2)和830°C(HA3)制备HA表面。人破骨细胞前体在不存在或存在M-SCF和RANKL的情况下进行培养。
HA表面具有相似的化学成分,然而,HA1和HA3分别呈现典型的微米级和纳米级结构形貌,HA2的形貌介于HA1和HA3之间。平均晶粒直径减小到纳米级范围(HA3)伴随着表面积、孔隙率和亲水性的增加以及粗糙度的降低。与HA1表面相比,HA3表面的破骨细胞黏附、分化和功能较低。细胞反应的差异似乎与相关细胞内信号通路的调节有关。
与HA微米级形貌相比,HA晶粒尺寸减小到仿生纳米级范围对破骨细胞分化和功能的吸引力似乎较小。
这一观察结果强调了表面形貌在设计先进生物材料以在再生策略中实现定制的骨细胞反应方面的作用。