TY - JOUR
T1 - Deep learning for non-invasive determination of the differentiation status of human neuronal cells by using phase-contrast photomicrographs
AU - Ooka, Maya
AU - Tokuoka, Yuta
AU - Nishimoto, Shori
AU - Hiroi, Noriko F.
AU - Yamada, Takahiro G.
AU - Funahashi, Akira
N1 - Funding Information:
This research was funded by Japan Society for the Promotion of Science KAKENHI grant number JP16H04731, JP19K22625. We are grateful to Nigel Mongan and Jennifer Lothion-Roy (The University of Nottingham) for English proofreading. Computations were performed mainly at the computer facilities at The University of Tokyo, Tokyo, Japan (Reedbush-H). Bayesian optimization was performed by using SigOpt (https://sigopt.com). We thank Takumi Hiraiwa from the Department of Biosciences and Informatics at Keio University, Tokyo, Japan, for his assistance with the experiments.
Publisher Copyright:
© 2019 by the authors.
PY - 2019/12/1
Y1 - 2019/12/1
N2 - Regenerative medicine using neural stem cells (NSCs), which self-renew and have pluripotency, has recently attracted a lot of interest. Much research has focused on the transplantation of differentiated NSCs to damaged tissues for the treatment of various neurodegenerative diseases and spinal cord injuries. However, current approaches for distinguishing differentiated from non-differentiated NSCs at the single-cell level have low reproducibility or are invasive to the cells. Here, we developed a fully automated, non-invasive convolutional neural network-based model to determine the differentiation status of human NSCs at the single-cell level from phase-contrast photomicrographs; after training, our model showed an accuracy of identification greater than 94%. To understand how our model distinguished between differentiated and non-differentiated NSCs, we evaluated the informative features it learned for the two cell types and found that it had learned several biologically relevant features related to NSC shape during differentiation. We also used our model to examine the differentiation of NSCs over time; the findings confirmed our model's ability to distinguish between non-differentiated and differentiated NSCs. Thus, our model was able to non-invasively and quantitatively identify differentiated NSCs with high accuracy and reproducibility, and, therefore, could be an ideal means of identifying differentiated NSCs in the clinic.
AB - Regenerative medicine using neural stem cells (NSCs), which self-renew and have pluripotency, has recently attracted a lot of interest. Much research has focused on the transplantation of differentiated NSCs to damaged tissues for the treatment of various neurodegenerative diseases and spinal cord injuries. However, current approaches for distinguishing differentiated from non-differentiated NSCs at the single-cell level have low reproducibility or are invasive to the cells. Here, we developed a fully automated, non-invasive convolutional neural network-based model to determine the differentiation status of human NSCs at the single-cell level from phase-contrast photomicrographs; after training, our model showed an accuracy of identification greater than 94%. To understand how our model distinguished between differentiated and non-differentiated NSCs, we evaluated the informative features it learned for the two cell types and found that it had learned several biologically relevant features related to NSC shape during differentiation. We also used our model to examine the differentiation of NSCs over time; the findings confirmed our model's ability to distinguish between non-differentiated and differentiated NSCs. Thus, our model was able to non-invasively and quantitatively identify differentiated NSCs with high accuracy and reproducibility, and, therefore, could be an ideal means of identifying differentiated NSCs in the clinic.
KW - Convolutional neural networks
KW - Deep learning
KW - Image-wise classification
KW - SH-SY5Y cells
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U2 - 10.3390/app9245503
DO - 10.3390/app9245503
M3 - Article
AN - SCOPUS:85077257466
SN - 2076-3417
VL - 9
JO - Applied Sciences (Switzerland)
JF - Applied Sciences (Switzerland)
IS - 24
M1 - 5503
ER -