Department of Bioengineering, University of Pittsburgh, Pittsburgh, PA 15219, United States.
Biomaterials. 2010 Jul;31(20):5345-54. doi: 10.1016/j.biomaterials.2010.03.052. Epub 2010 Apr 15.
Understanding how engineered tissue scaffold architecture affects cell morphology, metabolism, phenotypic expression, as well as predicting material mechanical behavior has recently received increased attention. In the present study, an image-based analysis approach that provides an automated tool to characterize engineered tissue fiber network topology is presented. Micro-architectural features that fully defined fiber network topology were detected and quantified, which include fiber orientation, connectivity, intersection spatial density, and diameter. Algorithm performance was tested using scanning electron microscopy (SEM) images of electrospun poly(ester urethane)urea (ES-PEUU) scaffolds. SEM images of rabbit mesenchymal stem cell (MSC) seeded collagen gel scaffolds and decellularized rat carotid arteries were also analyzed to further evaluate the ability of the algorithm to capture fiber network morphology regardless of scaffold type and the evaluated size scale. The image analysis procedure was validated qualitatively and quantitatively, comparing fiber network topology manually detected by human operators (n = 5) with that automatically detected by the algorithm. Correlation values between manual detected and algorithm detected results for the fiber angle distribution and for the fiber connectivity distribution were 0.86 and 0.93 respectively. Algorithm detected fiber intersections and fiber diameter values were comparable (within the mean +/- standard deviation) with those detected by human operators. This automated approach identifies and quantifies fiber network morphology as demonstrated for three relevant scaffold types and provides a means to: (1) guarantee objectivity, (2) significantly reduce analysis time, and (3) potentiate broader analysis of scaffold architecture effects on cell behavior and tissue development both in vitro and in vivo.
了解工程组织支架结构如何影响细胞形态、代谢、表型表达,并预测材料力学性能,最近受到了越来越多的关注。在本研究中,提出了一种基于图像的分析方法,该方法提供了一种自动工具来描述工程组织纤维网络拓扑结构。检测并量化了完全定义纤维网络拓扑结构的微观结构特征,包括纤维取向、连通性、交叉空间密度和直径。使用静电纺丝聚(酯脲)脲(ES-PEUU)支架的扫描电子显微镜(SEM)图像测试了算法性能。还分析了兔间充质干细胞(MSC)接种胶原凝胶支架和去细胞化大鼠颈动脉的 SEM 图像,以进一步评估该算法无论支架类型和评估大小如何,捕获纤维网络形态的能力。通过比较手动检测(n=5)和算法自动检测的纤维网络拓扑结构,对图像分析过程进行了定性和定量验证。纤维角度分布和纤维连通性分布的手动检测和算法检测结果之间的相关值分别为 0.86 和 0.93。算法检测到的纤维交叉点和纤维直径值与人工检测到的结果相当(平均值 +/- 标准差内)。这种自动方法可识别和量化纤维网络形态,如三种相关支架类型所示,并提供了一种手段:(1)保证客观性,(2)显著减少分析时间,(3)促进更广泛地分析支架结构对细胞行为和组织发育的影响,无论是在体外还是体内。