OneSC: A computational platform for recapitulating cell state transitions.
Da PengPatrick CahanPublished in: bioRxiv : the preprint server for biology (2024)
Computational modelling of cell state transitions has been a great interest of many in the field of developmental biology, cancer biology and cell fate engineering because it enables performing perturbation experiments in silico more rapidly and cheaply than could be achieved in a wet lab. Recent advancements in single-cell RNA sequencing (scRNA-seq) allow the capture of high- resolution snapshots of cell states as they transition along temporal trajectories. Using these high-throughput datasets, we can train computational models to generate in silico 'synthetic' cells that faithfully mimic the temporal trajectories. Here we present OneSC, a platform that can simulate synthetic cells across developmental trajectories using systems of stochastic differential equations govern by a core transcription factors (TFs) regulatory network. Different from the current network inference methods, OneSC prioritizes on generating Boolean network that produces faithful cell state transitions and steady cell states that mimic real biological systems. Applying OneSC to real data, we inferred a core TF network using a mouse myeloid progenitor scRNA-seq dataset and showed that the dynamical simulations of that network generate synthetic single-cell expression profiles that faithfully recapitulate the four myeloid differentiation trajectories going into differentiated cell states (erythrocytes, megakaryocytes, granulocytes and monocytes). Finally, through the in-silico perturbations of the mouse myeloid progenitor core network, we showed that OneSC can accurately predict cell fate decision biases of TF perturbations that closely match with previous experimental observations.
Keyphrases
- single cell
- high throughput
- rna seq
- cell fate
- cell therapy
- depressive symptoms
- transcription factor
- induced apoptosis
- dendritic cells
- squamous cell carcinoma
- bone marrow
- acute myeloid leukemia
- genome wide
- gene expression
- mass spectrometry
- stem cells
- signaling pathway
- oxidative stress
- immune response
- cell death
- cell cycle arrest
- peripheral blood
- machine learning
- molecular dynamics
- molecular dynamics simulations
- pi k akt
- electronic health record
- monte carlo