Cell Fate Forecasting: A Data-Assimilation Approach to Predict Epithelial-Mesenchymal Transition

被引:5
|
作者
Mendez, Mario J. [1 ,2 ]
Hoffman, Matthew J. [3 ]
Cherry, Elizabeth M. [3 ,4 ]
Lemmon, Christopher A. [2 ]
Weinberg, Seth H. [1 ,2 ,5 ]
机构
[1] Ohio State Univ, Dept Biomed Engn, Columbus, OH 43210 USA
[2] Virginia Commonwealth Univ, Dept Biomed Engn, Richmond, VA 23284 USA
[3] Rochester Inst Technol, Sch Math Sci, Rochester, NY 14623 USA
[4] Georgia Inst Technol, Sch Computat Sci & Engn, Atlanta, GA 30332 USA
[5] Ohio State Univ, Wexner Med Ctr, Dorothy M Davis Heart & Lung Res Inst, Columbus, OH 43210 USA
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
ENSEMBLE KALMAN FILTER; SYSTEM; EMT; PLASTICITY; EXPRESSION;
D O I
10.1016/j.bpj.2020.02.011
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Epithelial-mesenchymal transition (EMT) is a fundamental biological process that plays a central role in embryonic development, tissue regeneration, and cancer metastasis. Transforming growth factor-beta (TGF beta) is a potent inducer of this cellular transition, which is composed of transitions from an epithelial state to intermediate or partial EMT state(s) to a mesenchymal state. Using computational models to predict cell state transitions in a specific experiment is inherently difficult for reasons including model parameter uncertainty and error associated with experimental observations. In this study, we demonstrate that a data-assimilation approach using an ensemble Kalman filter, which combines limited noisy observations with predictions from a computational model of TGFO-beta-induced EMT, can reconstruct the cell state and predict the timing of state transitions. We used our approach in proof-of-concept "synthetic" insilico experiments, inwhich experimental observations were produced from a known computational model with the addition of noise. We mimic parameter uncertainty in in vitro experiments by incorporating model error that shifts the TGF beta doses associated with the state transitions and reproduces experimentally observed variability in cell state by either shifting a single parameter or generating "populations" of model parameters. We performed synthetic experiments for a wide range of TGF beta doses, investigating different cell steady-state conditions, and conducted parameter studies varying properties of the data-assimilation approach including the time interval between observations and incorporating multiplicative inflation, a technique to compensate for underestimation of the model uncertainty and mitigate the influence of model error. We find that cell state can be successfully reconstructed and the future cell state predicted in synthetic experiments, even inthe setting of model error, when experimental observations are performed at a sufficiently short time interval and incorporate multiplicative inflation. Our study demonstrates the feasibility and utility of a data-assimilation approach to forecasting the fate of cells undergoing EMT.
引用
收藏
页码:1749 / 1768
页数:20
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