Abstract

Lineage tracing involves the identification of all ancestors and descendants of a given cell, and is an important tool for studying biological processes such as development and disease progression. However, in many settings, controlled time-course experiments are not feasible, for example when working with tissue samples from patients. Here we present ImageAEOT, a computational pipeline based on autoencoders and optimal transport for predicting the lineages of cells using time-labeled datasets from different stages of a cellular process. Given a single-cell image from one of the stages, ImageAEOT generates an artificial lineage of this cell based on the population characteristics of the other stages. These lineages can be used to connect subpopulations of cells through the different stages and identify image-based features and biomarkers underlying the biological process. To validate our method, we apply ImageAEOT to a benchmark task based on nuclear and chromatin images during the activation of fibroblasts by tumor cells in engineered 3D tissues. We further validate ImageAEOT on chromatin images of various breast cancer cell lines and human tissue samples, thereby linking alterations in chromatin condensation patterns to different stages of tumor progression. Our results demonstrate the promise of computational methods based on autoencoding and optimal transport principles for lineage tracing in settings where existing experimental strategies cannot be used.

Highlights

  • BackgroundLineage tracing during differentiation, development and disease progression is critical for studying the underlying biological mechanisms

  • Our results demonstrate the promise of computational methods based on autoencoding and optimal transport principles for lineage tracing in settings where existing experimental strategies cannot be used

  • We present a novel strategy for reconstructing pseudo-lineages from high-dimensional single-cell datasets—ImageAEOT—which builds on Waddington-Optimal transport (OT) by using an autoencoder to embed single-cell data into an interpretable feature space in order to perform optimal transport

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Summary

Introduction

Development and disease progression is critical for studying the underlying biological mechanisms. Experimental strategies for lineage tracing include following cells over time using imaging or sequencing techniques after labelling them with synthetic or genetic markers [1,2,3]. Many single-cell experimental methodologies are destructive to samples and only provide snapshots of these cellular processes in time and from different cells. This calls for computational approaches to lineage tracing that generate pseudo-lineages of cells based on single-cell datasets collected across different time points

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