• English
    • français
  • Help
  •  | 
  • Contact
  •  | 
  • About
  •  | 
  • Login
  • HAL portal
  •  | 
  • Pages Pro
  • EN
  •  / 
  • FR
View Item 
  •   LillOA Home
  • Liste des unités
  • Centre de Recherche en Informatique, Signal et Automatique de Lille (CRIStAL) - UMR 9189
  • View Item
  •   LillOA Home
  • Liste des unités
  • Centre de Recherche en Informatique, Signal et Automatique de Lille (CRIStAL) - UMR 9189
  • View Item
JavaScript is disabled for your browser. Some features of this site may not work without it.

Elucidating the sources of β-catenin ...
  • BibTeX
  • CSV
  • Excel
  • RIS

Document type :
Article dans une revue scientifique: Article original
DOI :
10.1371/journal.pone.0042792
Title :
Elucidating the sources of β-catenin dynamics in human neural progenitor cells
Author(s) :
Mazemondet, Orianne [Auteur]
John, Mathias [Auteur]
Programming Languages for Biological Modeling and Simulation [BioComputing]
Leye, Stefan [Auteur]
Computer Science and Electrical Engineering
Uhrmacher, Adelinde [Auteur]
Computer Science and Electrical Engineering
Rolfs, Arndt [Auteur]
Journal title :
PLoS One
Publisher :
Public Library of Science
Publication date :
2012-08-20
ISSN :
1932-6203
HAL domain(s) :
Sciences du Vivant [q-bio]/Biochimie, Biologie Moléculaire/Réseaux moléculaires [q-bio.MN]
Informatique [cs]/Bio-informatique [q-bio.QM]
Sciences du Vivant [q-bio]/Bio-Informatique, Biologie Systémique [q-bio.QM]
English abstract : [en]
Human neural progenitor cells (hNPCs) form a new prospect for replacement therapies in the context of neurodegenerative diseases. The Wnt/β-catenin signaling pathway is known to be involved in the differentiation process ...
Show more >
Human neural progenitor cells (hNPCs) form a new prospect for replacement therapies in the context of neurodegenerative diseases. The Wnt/β-catenin signaling pathway is known to be involved in the differentiation process of hNPCs. In this paper, we present a computational modeling study on the dynamics of the Wnt/β-catenin signaling pathway in RVM cells, a common cell model of hNPCs. A concern when investigating RVM cells in vitro is that experimental results are possibly biased by the asynchrony of cell w.r.t. the cell cycle. To this end, we present a model of RVM cell populations that combines the Wnt/β-catenin signaling pathway with cell cycle control. Thereby, the model of the pathway in single cells is inspired by, extends on, and is validated by comparing to the reference model in literature. We present a study on the population model that compares simulation results to our own wet-lab data, obtained by Western-blot experiments. It starts with a stochastic investigation that reveals strong fluctuations in the dynamics of the pathway that directly result from model parameters provided in literature and that are not observable in deterministic investigations. These let us conclude that crucial mechanisms of noise reduction in the Wnt/β-catenin signaling pathway may still be unknown. We provide a new parameter set that is obtained by parameter fitting experiments and provides only insignificant fluctuations. Based on this, we present results that show that in in vitro experiments the impact of the cell cycle can be neglected. The results also suggest that in RVM cells a self-induced Wnt signal possibly occurs. We underline this point by a small extension of our model. Furthermore, we propose a couple of experimental set-ups to further investigate self-induced Wnt signaling in RVM cells, by this closing the cycle of computational systems biology.Show less >
Language :
Anglais
Peer reviewed article :
Oui
Audience :
Internationale
Popular science :
Non
Collections :
  • Centre de Recherche en Informatique, Signal et Automatique de Lille (CRIStAL) - UMR 9189
Source :
Harvested from HAL
Files
Thumbnail
  • https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0042792&type=printable
  • Open access
  • Access the document
Thumbnail
  • pdf
  • Open access
  • Access the document
Université de Lille

Mentions légales
Accessibilité : non conforme
Université de Lille © 2017