University of Maryland, Department of Physics, 1147 Physical Sciences Complex, College Park, MD, 20742, USA.
National Institute of Standards & Technology, Biosystems & Biomaterials Division, 100 Bureau Dr. Stop 8543, Gaithersburg, MD, 20899, USA.
Biomaterials. 2021 Jul;274:120812. doi: 10.1016/j.biomaterials.2021.120812. Epub 2021 Apr 26.
Nanofiber scaffolds can induce osteogenic differentiation and cell morphology alterations of human bone marrow stromal cells (hBMSCs) without introduction of chemical cues. In this study, we investigate the predictive power of day 1 cell morphology, quantified by a machine learning based method, as an indicator of osteogenic differentiation modulated by nanofiber density. Nanofiber scaffolds are fabricated via electrospinning. Microscopy, quantitative image processing and clustering analysis are used to systematically quantify scaffold properties as a function of fiber density. hBMSC osteogenic differentiation potential is evaluated after 14 days using osteogenic marker gene expression and after 50 days using calcium mineralization, showing enhanced osteogenic differentiation with an increase in nanofiber density. Cell morphology measurements at day 1 successfully predict differentiation potential when analyzed with the support vector machine (SVM)/supercell tools previously developed and trained on cells from a different donor. A correlation is observed between differentiation potential and cell morphology, demonstrating sensitivity of the morphology measurement to varying degrees of differentiation potential. To further understand how nanofiber density determines hBMSC morphology, both full 3-D morphology measurements as well as other measurements of the 2-D projected morphology are investigated in this study. To achieve predictive power on hBMSC osteogenic differentiation, at least two morphology metrics need to be considered together for each cell, with the majority of metric pairs including one 3-D morphology metric. Analysis of the local nanofiber structure surrounding each cell reveals a correlation with single-cell morphology and indicates that the osteogenic differentiation phenotype may be predictive at the single-cell level.
纳米纤维支架可以在不引入化学信号的情况下诱导人骨髓基质细胞(hBMSCs)的成骨分化和细胞形态改变。在这项研究中,我们研究了第 1 天细胞形态的预测能力,该能力通过基于机器学习的方法进行量化,作为纳米纤维密度调节成骨分化的指标。通过静电纺丝制备纳米纤维支架。使用显微镜、定量图像处理和聚类分析系统地定量支架特性作为纤维密度的函数。在第 14 天通过成骨标志物基因表达和第 50 天通过钙矿化来评估 hBMSC 成骨分化潜能,结果表明随着纳米纤维密度的增加,成骨分化能力增强。使用先前在来自不同供体的细胞上开发和训练的支持向量机(SVM)/超细胞工具对第 1 天的细胞形态测量进行分析,成功预测了分化潜能。分化潜能与细胞形态之间存在相关性,表明形态测量对分化潜能的不同程度具有敏感性。为了进一步了解纳米纤维密度如何决定 hBMSC 形态,本研究同时研究了全 3-D 形态测量以及 2-D 投影形态的其他测量。为了实现对 hBMSC 成骨分化的预测能力,每个细胞至少需要同时考虑两个形态指标,大多数指标对包括一个 3-D 形态指标。对每个细胞周围的局部纳米纤维结构的分析表明与单细胞形态相关,并且表明成骨分化表型可能具有预测单细胞水平的能力。