Optimal experimental design for mathematical models of haematopoiesis

Author:

Lomeli Luis Martinez1,Iniguez Abdon1,Tata Prasanthi2ORCID,Jena Nilamani2,Liu Zhong-Ying2,Van Etten Richard12345,Lander Arthur D.14567,Shahbaba Babak148,Lowengrub John S.14579,Minin Vladimir N.148ORCID

Affiliation:

1. Center for Complex Biological Systems, University of California Irvine, Irvine, CA, USA

2. Division of Hematology/Oncology, University of California Irvine, Irvine, CA, USA

3. Department of Biological Chemistry, University of California Irvine, Irvine, CA, USA

4. Center for Cancer Systems Biology, University of California Irvine, Irvine, CA, USA

5. Chao Family Comprehensive Cancer Center, University of California Irvine, Irvine, CA, USA

6. Department of Developmental and Cell Biology, University of California Irvine, Irvine, CA, USA

7. Department of Biomedical Engineering, University of California Irvine, Irvine, CA, USA

8. Department of Statistics, University of California Irvine, Irvine, CA, USA

9. Department of Mathematics, University of California Irvine, Irvine, CA, USA

Abstract

The haematopoietic system has a highly regulated and complex structure in which cells are organized to successfully create and maintain new blood cells. It is known that feedback regulation is crucial to tightly control this system, but the specific mechanisms by which control is exerted are not completely understood. In this work, we aim to uncover the underlying mechanisms in haematopoiesis by conducting perturbation experiments, where animal subjects are exposed to an external agent in order to observe the system response and evolution. We have developed a novel Bayesian hierarchical framework for optimal design of perturbation experiments and proper analysis of the data collected. We use a deterministic model that accounts for feedback and feedforward regulation on cell division rates and self-renewal probabilities. A significant obstacle is that the experimental data are not longitudinal, rather each data point corresponds to a different animal. We overcome this difficulty by modelling the unobserved cellular levels as latent variables. We then use principles of Bayesian experimental design to optimally distribute time points at which the haematopoietic cells are quantified. We evaluate our approach using synthetic and real experimental data and show that an optimal design can lead to better estimates of model parameters.

Funder

National Science Foundation

Fulbright-Garcia Robles

University of California Institute for Mexico and the United States

National Institutes of Health

Simons Foundation

Publisher

The Royal Society

Subject

Biomedical Engineering,Biochemistry,Biomaterials,Bioengineering,Biophysics,Biotechnology

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