Recognizing the Differentiation Degree of Human Induced Pluripotent Stem Cell-Derived Retinal Pigment Epithelium Cells Using Machine Learning and Deep Learning-Based Approaches.

Journal: Cells
Published Date:

Abstract

Induced pluripotent stem cells (iPSCs) can be differentiated into mesenchymal stem cells (iPSC-MSCs), retinal ganglion cells (iPSC-RGCs), and retinal pigmental epithelium cells (iPSC-RPEs) to meet the demand of regeneration medicine. Since the production of iPSCs and iPSC-derived cell lineages generally requires massive and time-consuming laboratory work, artificial intelligence (AI)-assisted approach that can facilitate the cell classification and recognize the cell differentiation degree is of critical demand. In this study, we propose the multi-slice tensor model, a modified convolutional neural network (CNN) designed to classify iPSC-derived cells and evaluate the differentiation efficiency of iPSC-RPEs. We removed the fully connected layers and projected the features using principle component analysis (PCA), and subsequently classified iPSC-RPEs according to various differentiation degree. With the assistance of the support vector machine (SVM), this model further showed capabilities to classify iPSCs, iPSC-MSCs, iPSC-RPEs, and iPSC-RGCs with an accuracy of 97.8%. In addition, the proposed model accurately recognized the differentiation of iPSC-RPEs and showed the potential to identify the candidate cells with ideal features and simultaneously exclude cells with immature/abnormal phenotypes. This rapid screening/classification system may facilitate the translation of iPSC-based technologies into clinical uses, such as cell transplantation therapy.

Authors

  • Chung-Yueh Lien
    Department of Information Management, National Taipei University of Nursing and Health Sciences, Taipei 112303, Taiwan.
  • Tseng-Tse Chen
    Department of Biomedical Engineering, National Yang Ming Chiao Tung University, Taipei 112304, Taiwan.
  • En-Tung Tsai
    Department of Medical Research, Taipei Veterans General Hospital, Taipei 112201, Taiwan.
  • Yu-Jer Hsiao
    Department of Medical Research, Taipei Veterans General Hospital, Taipei 112201, Taiwan.
  • Ni Lee
    Department of Medical Research, Taipei Veterans General Hospital, Taipei 112201, Taiwan.
  • Chong-En Gao
    Department of Medical Research, Taipei Veterans General Hospital, Taipei 112201, Taiwan.
  • Yi-Ping Yang
    Department of Medical Research, Taipei Veterans General Hospital, Taipei, Taiwan, ROC.
  • Shih-Jen Chen
    Department of Ophthalmology, Taipei Veterans General Hospital, Taipei, Taiwan.
  • Aliaksandr A Yarmishyn
    Department of Medical Research, Taipei Veterans General Hospital, Taipei, Taiwan.
  • De-Kuang Hwang
    Department of Ophthalmology, Taipei Veterans General Hospital, Taipei, Taiwan.
  • Shih-Jie Chou
    Faculty of Medicine, National Yang-Ming University, Taipei, Taiwan, ROC.
  • Woei-Chyn Chu
    National Yang Ming University, Taiwan (ROC) nova.wcc@gmail.com.
  • Shih-Hwa Chiou
    Department of Ophthalmology, Taipei Veterans General Hospital, Taipei, Taiwan.
  • Yueh Chien
    Department of Medical Research, Taipei Veterans General Hospital, Taipei, Taiwan, ROC.