Effect of Physicochemical Surface Properties of Silicon-Substituted Hydroxyapatite on Angiogenesis.

IF 2.7 4区 医学 Q3 CELL & TISSUE ENGINEERING Tissue engineering. Part C, Methods Pub Date : 2024-06-24 DOI:10.1089/ten.TEC.2024.0086
Else Ellermann, Ruth E Cameron, Serena M Best
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Abstract

Synthetic hydroxyapatite (HA) is a widely studied bioceramic for bone tissue engineering (BTE) due to its similarity to the mineral component of bone. As bone mineral contains various ionic substitutions that play a crucial role in bone metabolism, the bioactivity of HA can be improved by adding small amounts of physiologically relevant ions into its crystal structure, with silicate-substituted HA (Si-HA) showing particularly promising results. Nevertheless, it remains unclear how distinct material characteristics influence the bioactivity due to the intertwined nature of surface properties. A coculture methodology was optimized and applied for in vitro quantification of the biological response. Initially, HA and Si-HA samples were produced and characterized. To compare the bioactivity of the samples, a method was developed to measure interactions in an increasingly complex environment, first including fibronectin (FN) adsorption and subsequently cell adhesion in mono and coculture using primary human osteoblasts (hOBs) and human dermal microvascular endothelial cells (HDMECs), with and without FN precoating. An experimental set-up was designed to assess to what extent different surface features of the samples contribute to the induced biological response. An 8-nm gold sputter coating was applied to eradicate the electrochemical differences and polishing and abrading was used to reduce the differences in surface topographies. Overall, 1.25 wt% Si-HA exhibited most nanoscale variations in surface potential. In terms of bioactivity, 1.25 wt% Si-HA samples induced the highest osteoblast attachment and vessel formation. Additionally, in vitro vessel formation was established on Si-HA surfaces using a hOB:HDMEC cell ratio of 70:30 and a methodology was established that enabled the assessment of the relative effect of topographical and electrochemical features induced by silicon substitution in the HA lattice on their bioactivity. It was found that the difference in the amount of protein attached to HA and 1.25 wt% Si-HA after 2 h was affected by topographical differences. Conversely, electrochemical differences induced different vessel-like structure formation in coculture with a FN precoating. Without an FN precoating, both topographical and electrochemical differences dictated the differences in angiogenic response. Overall, 1.25 wt% Si-HA surface features appear to induce the most favorable protein adsorption and cell adhesion in mono and coculture with and without FN precoating.

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硅替代羟基磷灰石表面理化性质对血管生成的影响
合成羟基磷灰石(HA)因其与骨的矿物成分相似而成为骨组织工程(BTE)中被广泛研究的生物陶瓷。由于骨矿物质含有在骨代谢中起关键作用的各种离子替代物,因此可以通过在其晶体结构中添加少量与生理相关的离子来提高 HA 的生物活性,其中硅酸盐取代的 HA(Si-HA)尤其显示出良好的效果。然而,由于表面特性相互交织,目前仍不清楚不同的材料特性如何影响生物活性。我们优化了共培养方法,并将其用于体外量化生物反应。最初,我们制作了 HA 和 Si-HA 样品并对其进行了表征。为了比较样品的生物活性,开发了一种方法来测量在日益复杂的环境中的相互作用,首先包括纤维连接蛋白(FN)吸附,然后是使用原代人类成骨细胞(hOBs)和人类真皮微血管内皮细胞(HDMECs)在单培养和共培养中的细胞粘附,有无预涂 FN。我们设计了一套实验装置来评估样品的不同表面特征对诱导生物反应的影响程度。为了消除电化学差异,采用了 8 nm 的喷金涂层;为了减少表面形貌的差异,采用了抛光和研磨。总体而言,1.25wt% Si-HA的表面电位纳米级变化最大。在生物活性方面,1.25wt% Si-HA样品诱导成骨细胞附着和血管形成的能力最强。此外,还使用 hOB;HDMEC 细胞比为 70:30 的方法在 Si-HA 表面上建立了体外血管形成,并建立了一种方法来评估 HA 晶格中硅替代物引起的地形和电化学特征对其生物活性的相对影响。结果发现,2 小时后附着在 HA 和 1.25wt%Si-HA 上的蛋白质量的差异受到地形差异的影响。相反,在有 FN 预涂层的共培养中,电化学差异会诱导不同的血管样结构形成。在没有 FN 预涂层的情况下,地形和电化学差异决定了血管生成反应的不同。总之,1.25wt% Si-HA的表面特征似乎能在有FN预涂层和无FN预涂层的单培养和共培养中诱导最有利的蛋白质吸附和细胞粘附。
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来源期刊
Tissue engineering. Part C, Methods
Tissue engineering. Part C, Methods Medicine-Medicine (miscellaneous)
CiteScore
5.10
自引率
3.30%
发文量
136
期刊介绍: Tissue Engineering is the preeminent, biomedical journal advancing the field with cutting-edge research and applications that repair or regenerate portions or whole tissues. This multidisciplinary journal brings together the principles of engineering and life sciences in the creation of artificial tissues and regenerative medicine. Tissue Engineering is divided into three parts, providing a central forum for groundbreaking scientific research and developments of clinical applications from leading experts in the field that will enable the functional replacement of tissues. Tissue Engineering Methods (Part C) presents innovative tools and assays in scaffold development, stem cells and biologically active molecules to advance the field and to support clinical translation. Part C publishes monthly.
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