Faculty of Dentistry, University of Toronto, Toronto, ON, Canada; Institute for Biomaterials and Biomedical Engineering, University of Toronto, Toronto, ON, Canada; Princess Margaret Cancer Center, University Health Network, Toronto, ON, Canada.
Princess Margaret Cancer Center, University Health Network, Toronto, ON, Canada; Department of Medical Biophysics, University of Toronto, Toronto, ON, Canada.
Biomaterials. 2021 Jun;273:120837. doi: 10.1016/j.biomaterials.2021.120837. Epub 2021 Apr 20.
Surface topography drives the success of orthopedic and dental implants placed in bone, by directing the biology occurring at the tissue-implant interface. Over the last few decades, striking advancements have been made in the development of novel implant surfaces that enhance bone anchorage to their surfaces through contact osteogenesis: the combination of the two phenomena of recruitment and migration of mesenchymal progenitor cells to the implant surface, and their differentiation into bone-forming cells. While the latter is generally understood, the mechanisms and dynamics underlying the migration and recruitment of such progenitor cells into the wound site have garnered little attention. To address this deficit, we surgically inserted metallic implants with two different surface topographies into the skulls of mice, and then employed real-time spatiotemporal microscopic monitoring of the peri-implant tissue healing to track the ingress of cells. Our results show that nano-topographically complex, in comparison to relatively smooth, implant surfaces profoundly affect recruitment of both endothelial cells, which are essential for angiogenesis, and the mesenchymal progenitor cells that give rise to the reparative tissue stroma. The latter appear concomitantly in the wound site with endothelial cells, from the vascularized areas of the periosteum, and demonstrate a proliferative "bloom" that diminishes with time, although some of these cells differentiate into important stromal cells, pericytes and osteocytes, of the reparative wound. In separate experiments we show, using trajectory plots, that the directionality of migration for both endothelial and perivascular cells can be explained by implant surface dependent release of local cytokine gradients from platelets that would become activated on the implant surfaces during initial blood contact. These findings provide new biological insights into the earliest stages of wound healing, and have broad implications in the application of putative nano-topographically complex biomaterials in many tissue types.
表面形貌通过指导组织-植入物界面发生的生物学过程,从而决定了骨科和牙科植入物在骨中的成功。在过去的几十年中,通过接触成骨作用(即募集和间充质祖细胞向植入物表面迁移及其向成骨细胞分化这两种现象的结合)增强骨与植入物表面的锚定作用,新型植入物表面的开发取得了显著进展。虽然后者通常被理解,但这些祖细胞向创伤部位迁移和募集的机制和动力学却很少受到关注。为了解决这一不足,我们将具有两种不同表面形貌的金属植入物手术植入小鼠颅骨中,然后通过实时时空显微镜监测植入物周围组织的愈合情况来跟踪细胞的进入。我们的研究结果表明,与相对光滑的植入物表面相比,纳米形貌复杂的植入物表面会极大地影响血管内皮细胞和间充质祖细胞的募集,前者对于血管生成至关重要,后者则形成修复组织基质。后者与内皮细胞同时出现在创伤部位,来源于骨膜的血管化区域,并表现出一种增殖“繁荣”,随着时间的推移而减少,尽管其中一些细胞分化为修复性创伤中的重要基质细胞、周细胞和成骨细胞。在单独的实验中,我们通过轨迹图表明,内皮细胞和血管周围细胞的迁移方向可以通过依赖于植入物表面的局部细胞因子梯度的释放来解释,这些细胞因子梯度来自于在最初的血液接触过程中在植入物表面上被激活的血小板。这些发现为伤口愈合的早期阶段提供了新的生物学见解,并对许多组织类型中潜在的纳米形貌复杂生物材料的应用具有广泛的意义。