Parallel Networks to simulate complex multicellular dynamics - A proof of concept with intervertebral disc cell systems
Baumgartner, L.; Gonzalez Ballester, M. A.; Noailly, J.
Show abstract
BackgroundNetwork models are convenient to represent in a mechanistic way the complexity of cell biological activity. Dynamic simulations of such networks might require approximations of equation parameters through reverse engineering, numerous and costly experimental research, and/or have limited capacity to explore cell responses to chronic, dose-dependent stimulus exposure. Here we present a mechanistic methodology allowing the simulation of interrelated cell responses of multicellular systems to multifactorial stimuli with dose-and time dependent network links. Methodsa mathematical framework to approach systems biology research questions is presented, the Parallel Networks (PN)-Methodology. It consists of a novel concept, where multicellular systems are described as many relatively small feed-forward networks acting in parallel. Each parallel network is calculated through a specifically designed ordinary differential equation (ODE). Through a unique approach to feed the ODE with interrelated parameters, a system of decoupled, analytically resolvable ODE was obtained. ResultsApplied to intervertebral disc multicellular systems, virtual environments of multifactorial stimuli and multiple cell responses simulating daily moving activities, and to microgravity could successfully be created. ConclusionsThe PN-Methodology stands for a one-of-a-kind mathematical methodology to approximate dynamics of complex multicellular systems over long periods of time at low computational costs.
Matching journals
The top 8 journals account for 50% of the predicted probability mass.
Similar papers in this journal
- Dose-dependent thresholds of dexamethasone destabilize CAR T-cell treatment efficacy 94%
- Notch signaling and taxis mechanims regulate early stage angiogenesis: A mathematical and computational model 94%
- The role of actin protrusion dynamics in cell migration through a degradable viscoelastic extracellular matrix: Insights from a computational model 94%
Similar papers in this journal
- Computational quantification of global effects induced by mutations and drugs in signaling networks of colorectal cancer cells. 94%
- Computational Evidence For Multi-Layer Crosstalk Between The Cadherin-11 And Pdgfr Pathways 94%
- Model Parameter identification using 2D vs 3D experimental data: a comparative analysis 94%
Similar papers in this journal
- Frequency preference response in covalent modification cycles under substrate sequestration conditions 94%
- Optimal Performance Objectives in the Highly Conserved Bone Morphogenetic Protein Signaling Pathway 93%
- Cell polarisation in a bulk-surface model can be driven by both classic and non-classic Turing instability 93%
Similar papers in this journal
"Similar papers" are the closest papers from that journal in the model's embedding space. They show what the match is built on, but the ranking comes mostly from a classifier over the whole training set, not from these examples alone.