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A new holistic 3D non-invasive analysis of cellular distribution and motility on fibroin-alginate microcarriers using light sheet fluorescent microscopy

机译:使用光片荧光显微镜对纤维蛋白-藻酸盐微载体上细胞分布和运动性进行全新的整体3D非侵入性分析

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摘要

Cell interaction with biomaterials is one of the keystones to developing medical devices for tissue engineering applications. Biomaterials are the scaffolds that give three-dimensional support to the cells, and are vectors that deliver the cells to the injured tissue requiring repair. Features of biomaterials can influence the behaviour of the cells and consequently the efficacy of the tissue-engineered product. The adhesion, distribution and motility of the seeded cells onto the scaffold represent key aspects, and must be evaluated in vitro during the product development, especially when the efficacy of a specific tissue-engineered product depends on viable and functional cell loading. In this work, we propose a non-invasive and non-destructive imaging analysis for investigating motility, viability and distribution of Mesenchymal Stem Cells (MSCs) on silk fibroin-based alginate microcarriers, to test the adhesion capacity of the fibroin coating onto alginate which is known to be unsuitable for cell adhesion. However, in depth characterization of the biomaterial is beyond the scope of this paper. Scaffold-loaded MSCs were stained with Calcein-AM and Ethidium homodimer-1 to detect live and dead cells, respectively, and counterstained with Hoechst to label cell nuclei. Time-lapse Light Sheet Fluorescent Microscopy (LSFM) was then used to produce three-dimensional images of the entire cells-loaded fibroin/alginate microcarriers. In order to quantitatively track the cell motility over time, we also developed an open source user friendly software tool called Fluorescent Cell Tracker in Three-Dimensions (F-Tracker3D). Combining LSFM with F-Tracker3D we were able for the first time to assess the distribution and motility of stem cells in a non-invasive, non-destructive, quantitative, and three-dimensional analysis of the entire surface of the cell-loaded scaffold. We therefore propose this imaging technique as an innovative holistic tool for monitoring cell-biomaterial interactions, and as a tool for the design, fabrication and functionalization of a scaffold as a medical device.
机译:细胞与生物材料的相互作用是开发用于组织工程应用的医疗设备的基石之一。生物材料是为细胞提供三维支撑的支架,并且是将细胞递送至需要修复的受损组织的载体。生物材料的特征会影响细胞的行为,从而影响组织工程产品的功效。种子细胞在支架上的粘附,分布和运动性是关键方面,必须在产品开发过程中进行体外评估,尤其是当特定组织工程产品的功效取决于活细胞和功能性细胞负荷时。在这项工作中,我们提出了一种非侵入性和非破坏性的成像分析,用于研究基于丝素蛋白的藻酸盐微载体上的间充质干细胞(MSC)的运动性,生存力和分布,以测试血纤蛋白涂层对藻酸盐的粘附能力已知不适合细胞粘附。但是,生物材料的深度表征超出了本文的范围。用Calcein-AM和Ethidium homodimer-1对装载有支架的MSC进行染色,分别检测活细胞和死细胞,并用Hoechst复染以标记细胞核。然后使用延时光片荧光显微镜(LSFM)生成加载了整个细胞的丝蛋白/藻酸盐微载体的三维图像。为了定量跟踪随时间变化的细胞运动,我们还开发了一种开源的用户友好软件工具,称为三维荧光细胞跟踪器(F-Tracker3D)。将LSFM与F-Tracker3D结合起来,我们首次能够在对载有细胞的支架整个表面进行无创,无损,定量和三维分析的情况下评估干细胞的分布和运动性。因此,我们提出该成像技术作为用于监视细胞-生物材料相互作用的创新整体工具,以及作为支架,医疗设备的设计,制造和功能化的工具。

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