Quality Control of Human Pluripotent Stem Cell Colonies by Computational Image Analysis Using Convolutional Neural Networks

被引:5
作者
Mamaeva, Anastasiya [1 ]
Krasnova, Olga [2 ]
Khvorova, Irina [3 ]
Kozlov, Konstantin [1 ]
Gursky, Vitaly [4 ]
Samsonova, Maria [1 ]
Tikhonova, Olga [5 ]
Neganova, Irina [2 ]
机构
[1] Peter Great St Petersburg Polytech Univ, Math Biol & Bioinformat Lab, St Petersburg 195251, Russia
[2] Inst Cytol, St Petersburg 194064, Russia
[3] St Petersburg State Univ, Fac Biol, St Petersburg 199034, Russia
[4] Ioffe Inst, St Petersburg 194021, Russia
[5] Inst Biomed Chem, Moscow 119121, Russia
基金
俄罗斯科学基金会;
关键词
human pluripotent stem cells; pluripotency; deep learning; convolutional neural networks; image processing; CULTURE; DIFFERENTIATION; DERIVATION;
D O I
10.3390/ijms24010140
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Human pluripotent stem cells are promising for a wide range of research and therapeutic purposes. Their maintenance in culture requires the deep control of their pluripotent and clonal status. A non-invasive method for such control involves day-to-day observation of the morphological changes, along with imaging colonies, with the subsequent automatic assessment of colony phenotype using image analysis by machine learning methods. We developed a classifier using a convolutional neural network and applied it to discriminate between images of human embryonic stem cell (hESC) colonies with "good" and "bad" morphological phenotypes associated with a high and low potential for pluripotency and clonality maintenance, respectively. The training dataset included the phase-contrast images of hESC line H9, in which the morphological phenotype of each colony was assessed through visual analysis. The classifier showed a high level of accuracy (89%) in phenotype prediction. By training the classifier on cropped images of various sizes, we showed that the spatial scale of similar to 144 mu m was the most informative in terms of classification quality, which was an intermediate size between the characteristic diameters of a single cell (similar to 15 mu m) and the entire colony (similar to 540 mu m). We additionally performed a proteomic analysis of several H9 cell samples used in the computational analysis and showed that cells of different phenotypes differentiated at the molecular level. Our results indicated that the proposed approach could be used as an effective method of non-invasive automated analysis to identify undesirable developmental anomalies during the propagation of pluripotent stem cells.
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页数:12
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