Juhl Otto J, Merife Anna-Blessing, Zhang Yue, Lemmon Christopher A, Donahue Henry J
Department of Biomedical Engineering and Institute for Engineering and Medicine, Virginia Commonwealth University, Richmond, VA, United States.
Front Bioeng Biotechnol. 2021 Jan 8;8:591084. doi: 10.3389/fbioe.2020.591084. eCollection 2020.
Substrate surface characteristics such as roughness, wettability and particle density are well-known contributors of a substrate's overall osteogenic potential. These characteristics are known to regulate cell mechanics as well as induce changes in cell stiffness, cell adhesions, and cytoskeletal structure. Pro-osteogenic particles, such as hydroxyapatite, are often incorporated into a substrate to enhance the substrates osteogenic potential. However, it is unknown which substrate characteristic is the key regulator of osteogenesis. This is partly due to the lack of understanding of how these substrate surface characteristics are transduced by cells. In this study substrates composed of polycaprolactone (PCL) and carbonated hydroxyapatite particles (HAp) were synthesized. HAp concentration was varied, and a range of surface characteristics created. The effect of each substrate characteristic on osteoblastic differentiation was then examined. We found that, of the characteristics examined, only HAp density, and indeed a specific density (85 particles/cm), significantly increased osteoblastic differentiation. Further, an increase in focal adhesion maturation and turnover was observed in cells cultured on this substrate. Moreover, β-catenin translocation from the membrane bound cell fraction to the nucleus was more rapid in cells on the 85 particle/cm substrate compared to cells on tissue culture polystyrene. Together, these data suggest that particle density is one pivotal factor in determining a substrates overall osteogenic potential. Additionally, the observed increase in osteoblastic differentiation is a at least partly the result of β-catenin translocation and transcriptional activity suggesting a β-catenin mediated mechanism by which substrate surface characteristics are transduced.
诸如粗糙度、润湿性和颗粒密度等基质表面特征是基质整体成骨潜力的众所周知的影响因素。已知这些特征可调节细胞力学,并诱导细胞硬度、细胞粘附和细胞骨架结构的变化。促骨生成颗粒,如羟基磷灰石,通常被掺入基质中以增强基质的成骨潜力。然而,尚不清楚哪种基质特征是成骨的关键调节因子。部分原因是缺乏对这些基质表面特征如何被细胞转导的理解。在本研究中,合成了由聚己内酯(PCL)和碳酸羟基磷灰石颗粒(HAp)组成的基质。改变HAp浓度,创造一系列表面特征。然后检查每种基质特征对成骨细胞分化的影响。我们发现,在所检查的特征中,只有HAp密度,实际上是特定密度(85个颗粒/平方厘米),显著增加了成骨细胞分化。此外,在这种基质上培养的细胞中观察到粘着斑成熟和周转增加。而且,与在组织培养聚苯乙烯上的细胞相比,在85颗粒/平方厘米基质上的细胞中β-连环蛋白从膜结合细胞部分向细胞核的转位更快。总之,这些数据表明颗粒密度是决定基质整体成骨潜力的一个关键因素。此外,观察到的成骨细胞分化增加至少部分是β-连环蛋白转位和转录活性的结果,这表明存在一种β-连环蛋白介导的机制,通过该机制基质表面特征被转导。