Mota Sakina M, Rogers Robert E, Haskell Andrew W, McNeill Eoin P, Kaunas Roland, Gregory Carl A, Giger Maryellen L, Maitland Kristen C
Texas A&M University, Department of Biomedical Engineering, College Station, Texas, United States.
Texas A&M Health Science Center, College of Medicine, Bryan, Texas, United States.
J Med Imaging (Bellingham). 2021 Jan;8(1):014503. doi: 10.1117/1.JMI.8.1.014503. Epub 2021 Feb 1.
: Mesenchymal stem cells (MSCs) have demonstrated clinically relevant therapeutic effects for treatment of trauma and chronic diseases. The proliferative potential, immunomodulatory characteristics, and multipotentiality of MSCs in monolayer culture is reflected by their morphological phenotype. Standard techniques to evaluate culture viability are subjective, destructive, or time-consuming. We present an image analysis approach to objectively determine morphological phenotype of MSCs for prediction of culture efficacy. : The algorithm was trained using phase-contrast micrographs acquired during the early and mid-logarithmic stages of MSC expansion. Cell regions are localized using edge detection, thresholding, and morphological operations, followed by cell marker identification using H-minima transform within each region to differentiate individual cells from cell clusters. Clusters are segmented using marker-controlled watershed to obtain single cells. Morphometric and textural features are extracted to classify cells based on phenotype using machine learning. : Algorithm performance was validated using an independent test dataset of 186 MSCs in 36 culture images. Results show 88% sensitivity and 86% precision for overall cell detection and a mean Sorensen-Dice coefficient of for segmentation per image. The algorithm exhibited an area under the curve of 0.816 ( to 0.886) and 0.787 ( to 0.851) for classifying MSCs according to their phenotype at early and mid-logarithmic expansion, respectively. : The proposed method shows potential to segment and classify low and moderately dense MSCs based on phenotype with high accuracy and robustness. It enables quantifiable and consistent morphology-based quality assessment for various culture protocols to facilitate cytotherapy development.
间充质干细胞(MSCs)已在创伤和慢性病治疗中展现出具有临床意义的治疗效果。MSCs在单层培养中的增殖潜力、免疫调节特性和多能性通过其形态表型得以体现。评估培养活力的标准技术主观、具有破坏性或耗时。我们提出一种图像分析方法,以客观确定MSCs的形态表型,从而预测培养效果。该算法使用在MSCs扩增的对数早期和中期获取的相差显微镜图像进行训练。通过边缘检测、阈值处理和形态学操作定位细胞区域,然后在每个区域内使用H极小值变换识别细胞标记,以区分单个细胞与细胞簇。使用标记控制的分水岭算法分割细胞簇以获得单个细胞。提取形态和纹理特征,利用机器学习根据表型对细胞进行分类。使用包含36张培养图像中186个MSCs的独立测试数据集验证算法性能。结果显示,整体细胞检测的灵敏度为88%,精度为86%,每张图像分割的平均索伦森 - 迪赛系数为[具体数值缺失]。在对数早期和中期扩增阶段,根据MSCs表型进行分类时,该算法的曲线下面积分别为0.816([具体范围缺失]至0.886)和0.787([具体范围缺失]至0.851)。所提出的方法显示出基于表型对低密度和中等密度MSCs进行高精度和稳健分割及分类的潜力。它能够对各种培养方案进行基于形态学的可量化且一致的质量评估,以促进细胞治疗的发展。