Email updates

Keep up to date with the latest news and content from BMC Systems Biology and BioMed Central.

Open Access Highly Accessed Research article

Modeling system states in liver cells: Survival, apoptosis and their modifications in response to viral infection

Nicole Philippi1, Dorothee Walter2, Rebekka Schlatter3, Karine Ferreira2, Michael Ederer3, Oliver Sawodny3, Jens Timmer4, Christoph Borner2 and Thomas Dandekar1*

Author Affiliations

1 Dept of bioinformatics, Biocenter, Am Hubland, University of Würzburg, 97074 Würzburg, Germany

2 Institute of Molecular Medicine and Cell Research (ZBMZ), Albert Ludwigs University Freiburg, 79104 Freiburg, Germany

3 Institute for System Dynamics, University of Stuttgart, Pfaffenwaldring 9, 70569 Stuttgart, Germany

4 Freiburger Zentrum für Datenanalyse und Modellbildung (FDM), Albert Ludwigs University Freiburg, 79070 Freiburg, Germany

For all author emails, please log on.

BMC Systems Biology 2009, 3:97  doi:10.1186/1752-0509-3-97

Published: 22 September 2009

Abstract

Background

The decision pro- or contra apoptosis is complex, involves a number of different inputs, and is central for the homeostasis of an individual cell as well as for the maintenance and regeneration of the complete organism.

Results

This study centers on Fas ligand (FasL)-mediated apoptosis, and a complex and internally strongly linked network is assembled around the central FasL-mediated apoptosis cascade. Different bioinformatical techniques are employed and different crosstalk possibilities including the integrin pathway are considered. This network is translated into a Boolean network (74 nodes, 108 edges). System stability is dynamically sampled and investigated using the software SQUAD. Testing a number of alternative crosstalk possibilities and networks we find that there are four stable system states, two states comprising cell survival and two states describing apoptosis by the intrinsic and the extrinsic pathways, respectively. The model is validated by comparing it to experimental data from kinetics of cytochrome c release and caspase activation in wildtype and Bid knockout cells grown on different substrates. Pathophysiological modifications such as input from cytomegalovirus proteins M36 and M45 again produces output behavior that well agrees with experimental data.

Conclusion

A network model for apoptosis and crosstalk in hepatocytes shows four different system states and reproduces a number of different conditions around apoptosis including effects of different growth substrates and viral infections. It produces semi-quantitative predictions on the activity of individual nodes, agreeing with experimental data. The model (SBML format) and all data are available for further predictions and development.