ArticlePLoS computational biology2013
Spatial pattern dynamics of 3D stem cell loss of pluripotency via rules-based computational modeling.
Article in PLoS computational biology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.
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Who cites it
19 citing papers in PubMed.
- Topological data analysis of pattern formation of human induced pluripotent stem cell colonies.Scientific reports · 2025Article
- Recognition and reconstruction of cell differentiation patterns with deep learning.PLoS computational biology · 2023Article
- Adjusting the range of cell-cell communication enables fine-tuning of cell fate patterns from checkerboard to engulfing.Journal of mathematical biology · 2023Article
- Engineering multicellular living systems-a Keystone Symposia report.Annals of the New York Academy of Sciences · 2022Article
- Deep neural net tracking of human pluripotent stem cells reveals intrinsic behaviors directing morphogenesis.Stem cell reports · 2021Article
- Automated Design of Pluripotent Stem Cell Self-Organization.Cell systems · 2019Article
- Agent-based modeling of morphogenetic systems: Advantages and challenges.PLoS computational biology · 2019Review
- Mouse ICM Organoids Reveal Three-Dimensional Cell Fate Clustering.Biophysical journal · 2019Article
- Dynamic intercellular transport modulates the spatial patterning of differentiation during early neural commitment.Nature communications · 2018Article
- Probing the stochastic property of endoreduplication in cell size determination of Arabidopsis thaliana leaf epidermal tissue.PloS one · 2017Article
- Inverse problem analysis of pluripotent stem cell aggregation dynamics in stirred-suspension cultures.Journal of biotechnology · 2015Article
- Quantitative multivariate analysis of dynamic multicellular morphogenic trajectories.Integrative biology : quantitative biosciences from nano to macro · 2015Article
- An agent-based model of cancer stem cell initiated avascular tumour growth and metastasis: the effect of seeding frequency and location.Journal of the Royal Society, Interface · 2014Article
- Single-cell analysis of embryoid body heterogeneity using microfluidic trapping array.Biomedical microdevices · 2014Article
- Engineering three-dimensional stem cell morphogenesis for the development of tissue models and scalable regenerative therapeutics.Annals of biomedical engineering · 2014Review
- Stem cells in a three-dimensional scaffold environment.SpringerPlus · 2014Review
- Deconstructing stem cell population heterogeneity: single-cell analysis and modeling approaches.Biotechnology advances · 2013Review
- Time scales in epigenetic dynamics and phenotypic heterogeneity of embryonic stem cells.PLoS computational biology · 2013Article
- Derivative-Free Optimization of Rate Parameters of Capsid Assembly Models from Bulk in Vitro Data.IEEE/ACM transactions on computational biology and bioinformaticsArticle
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4 authors.
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Abstract
Pluripotent embryonic stem cells (ESCs) have the unique ability to differentiate into cells from all germ lineages, making them a potentially robust cell source for regenerative medicine therapies, but difficulties in predicting and controlling ESC differentiation currently limit the development of therapies and applications from such cells. A common approach to induce the differentiation of ESCs in vitro is via the formation of multicellular aggregates known as embryoid bodies (EBs), yet cell fate specification within EBs is generally considered an ill-defined and poorly controlled process. Thus, the objective of this study was to use rules-based cellular modeling to provide insight into which processes influence initial cell fate transitions in 3-dimensional microenvironments. Mouse embryonic stem cells (D3 cell line) were differentiated to examine the temporal and spatial patterns associated with loss of pluripotency as measured through Oct4 expression. Global properties of the multicellular aggregates were accurately recapitulated by a physics-based aggregation simulation when compared to experimentally measured physical parameters of EBs. Oct4 expression patterns were analyzed by confocal microscopy over time and compared to simulated trajectories of EB patterns. The simulations demonstrated that loss of Oct4 can be modeled as a binary process, and that associated patterns can be explained by a set of simple rules that combine baseline stochasticity with intercellular communication. Competing influences between Oct4+ and Oct4- neighbors result in the observed patterns of pluripotency loss within EBs, establishing the utility of rules-based modeling for hypothesis generation of underlying ESC differentiation processes. Importantly, the results indicate that the rules dominate the emergence of patterns independent of EB structure, size, or cell division. In combination with strategies to engineer cellular microenvironments, this type of modeling approach is a powerful tool to predict stem cell behavior under a number of culture conditions that emulate characteristics of 3D stem cell niches.
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