Abstract

The hematopoietic stem cells (HSCs) can differentiate to myeloid and lymphoid lineages, which lead to more specific differentiated cells. This cell fate decision process is governed by an underlying gene regulatory network. However, its underlying mechanism remains to be fully clarified. In this work, based on a gene regulatory network of HSC differentiation, we built a dynamical model and developed an optimization approach to infer model parameters by fitting experimental data quantitatively. We mapped out the potential landscape of HSC differentiation and identified multistable cell states observed in experiments, including multipotent progenitor, B-cell, and macrophage. Interestingly, we also identified one new intermediate cell state on the landscape, which plays a critical role on the cellular transdifferentiation. By calculating the transition action among different attractor states, we quantified kinetic transition paths for differentiation and transdifferentiation between different cell states and identified key genes and regulations during these transition processes. Our work provides a general approach to construct a gene regulatory network model based on experimental data and new insights into the roles of intermediate states on the transdifferentiation process in HSC development.2 MoreReceived 22 September 2020Accepted 9 February 2021DOI:https://doi.org/10.1103/PhysRevResearch.3.013186Published by the American Physical Society under the terms of the Creative Commons Attribution 4.0 International license. Further distribution of this work must maintain attribution to the author(s) and the published article's title, journal citation, and DOI.Published by the American Physical SocietyPhysics Subject Headings (PhySH)Research AreasComplex systemsPhysical SystemsGene regulatory networksNonequilibrium systemsInterdisciplinary PhysicsNetworksBiological Physics

Highlights

  • Hematopoietic stem cells (HSCs), which are capable of self-renewal and differentiating into almost all blood cell lineages, served as a paradigm for understanding stem cell development [1,2]

  • We mapped out the potential landscape of hematopoietic stem cells (HSCs) differentiation and identified multistable cell states observed in experiments, including multipotent progenitor, B-cell, and macrophage

  • Our work provides a general approach to construct a gene regulatory network model based on experimental data and new insights into the roles of intermediate states on the transdifferentiation process in HSC development

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Summary

Introduction

Hematopoietic stem cells (HSCs), which are capable of self-renewal and differentiating into almost all blood cell lineages, served as a paradigm for understanding stem cell development [1,2]. Mathematical modeling approaches are gradually introduced to study gene regulatory networks and capture temporal evolving characteristics of the system [7]. Computational models are used to reconstruct the gene regulatory network of HSC systems [8]. Boolean models of gene regulatory networks have been used to study the differentiation mechanisms and identify key interactions in cell fate commitment [9,10]. To understand the process of cell fate decisions, Waddington proposed a landscape concept as a metaphor to explain the development and differentiation of cells [14]. In Waddington landscape theory, the developmental process is viewed as a ball rolling from one basin representing stem cell states to the basins representing differentiated cell states.

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