Institute for Biomedical Materials and Devices, Faculty of Science , University of Technology Sydney , Sydney , NSW 2007 , Australia.
The Ritchie Centre , Hudson Institute of Medical Research , Clayton 3168 , Australia.
ACS Appl Mater Interfaces. 2018 Jul 25;10(29):24840-24849. doi: 10.1021/acsami.8b08029. Epub 2018 Jul 11.
Bone osteogenesis is a complex phenomenon dependent on numerous microenvironmental cues, with their synchrony regulating cellular functions, such as mechanical signaling, survival, proliferation, and differentiation, as well as controlled regional specification of skeletal progenitor cell fate. Therefore, obtaining a mechanistic understanding of cellular response to a microenvironment is now coming into intense focus, which will facilitate the design of programmable biomaterials for regenerative medicine. State-of-the-art nanomaterial synthesis and self-assembly processes yield complex structures that mimic surface properties, composition, and partially the morphology of the extracellular matrix. However, determining key structural properties that control cell attachment has been challenging and contradictory results are reported regarding the mechanisms and roll of nanostructured materials. Here, we significantly improve osteogenesis on bioinert substrates, demonstrating an exemplary organic-inorganic interface for superior prosthesis biointegration. We identify critical microscale hierarchical features that drastically enhance the cellular response to the same nanoscale architecture. It was observed that hierarchical morphologies, with a porosity above 80%, promote early-stage osteoinduction, as indicated by extensive coating ingrowth and nanofilopodia formation. We determined that cellular integration was mediated by two-way recognition of specific nano- and microtopographical cues between the host tissue and cellular microenvironment. This has allowed us to detail a set of determinant features for the nanofabrication of advanced prosthesis coatings that may ultimately improve implant longevity.
骨生成是一个复杂的现象,依赖于许多微环境线索,它们的同步调节细胞功能,如机械信号、存活、增殖和分化,以及骨骼祖细胞命运的受控区域特异性。因此,现在人们强烈关注对细胞对微环境的反应的机制理解,这将有助于设计用于再生医学的可编程生物材料。最先进的纳米材料合成和自组装工艺产生了复杂的结构,这些结构模拟了表面特性、组成,以及部分细胞外基质的形态。然而,确定控制细胞附着的关键结构特性一直具有挑战性,并且关于纳米结构材料的机制和作用的结果存在矛盾。在这里,我们显著改善了生物惰性基质上的成骨作用,为优异的假体生物整合展示了一个典范的有机-无机界面。我们确定了关键的微观分层特征,这些特征极大地增强了细胞对相同纳米级结构的反应。观察到具有 80%以上孔隙率的分层形态促进了早期的成骨诱导,表现为广泛的涂层向内生长和纳米丝状伪足形成。我们确定细胞整合是由宿主组织和细胞微环境之间的特定纳米和微形貌线索的双向识别介导的。这使我们能够详细说明一组用于先进假体涂层纳米制造的决定特征,这些特征最终可能提高植入物的使用寿命。