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Recognition and reconstruction of cell differentiation patterns with deep learning.

Authors :
Dirk R
Fischer JL
Schardt S
Ankenbrand MJ
Fischer SC
Source :
PLoS computational biology [PLoS Comput Biol] 2023 Oct 27; Vol. 19 (10), pp. e1011582. Date of Electronic Publication: 2023 Oct 27 (Print Publication: 2023).
Publication Year :
2023

Abstract

Cell lineage decisions occur in three-dimensional spatial patterns that are difficult to identify by eye. There is an ongoing effort to replicate such patterns using mathematical modeling. One approach uses long ranging cell-cell communication to replicate common spatial arrangements like checkerboard and engulfing patterns. In this model, the cell-cell communication has been implemented as a signal that disperses throughout the tissue. On the other hand, machine learning models have been developed for pattern recognition and pattern reconstruction tasks. We combined synthetic data generated by the mathematical model with spatial summary statistics and deep learning algorithms to recognize and reconstruct cell fate patterns in organoids of mouse embryonic stem cells. Application of Moran's index and pair correlation functions for in vitro and synthetic data from the model showed local clustering and radial segregation. To assess the patterns as a whole, a graph neural network was developed and trained on synthetic data from the model. Application to in vitro data predicted a low signal dispersion value. To test this result, we implemented a multilayer perceptron for the prediction of a given cell fate based on the fates of the neighboring cells. The results show a 70% accuracy of cell fate imputation based on the nine nearest neighbors of a cell. Overall, our approach combines deep learning with mathematical modeling to link cell fate patterns with potential underlying mechanisms.<br />Competing Interests: The authors have declared that no competing interests exist.<br /> (Copyright: © 2023 Dirk et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.)

Details

Language :
English
ISSN :
1553-7358
Volume :
19
Issue :
10
Database :
MEDLINE
Journal :
PLoS computational biology
Publication Type :
Academic Journal
Accession number :
37889897
Full Text :
https://doi.org/10.1371/journal.pcbi.1011582