Cargando…
An agent-based model of the Notch signaling pathway elucidates three levels of complexity in the determination of developmental patterning
BACKGROUND: The Notch signaling pathway is involved in cell fate decision and developmental patterning in diverse organisms. A receptor molecule, Notch (N), and a ligand molecule (in this case Delta or Dl) are the central molecules in this pathway. In early Drosophila embryos, these molecules determ...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6332573/ https://www.ncbi.nlm.nih.gov/pubmed/30642357 http://dx.doi.org/10.1186/s12918-018-0672-9 |
_version_ | 1783387382090825728 |
---|---|
author | Reynolds, Elaine R. Himmelwright, Ryan Sanginiti, Christopher Pfaffmann, Jeffrey O. |
author_facet | Reynolds, Elaine R. Himmelwright, Ryan Sanginiti, Christopher Pfaffmann, Jeffrey O. |
author_sort | Reynolds, Elaine R. |
collection | PubMed |
description | BACKGROUND: The Notch signaling pathway is involved in cell fate decision and developmental patterning in diverse organisms. A receptor molecule, Notch (N), and a ligand molecule (in this case Delta or Dl) are the central molecules in this pathway. In early Drosophila embryos, these molecules determine neural vs. skin fates in a reproducible rosette pattern. RESULTS: We have created an agent-based model (ABM) that simulates the molecular components for this signaling pathway as agents acting within a spatial representation of a cell. The model captures the changing levels of these components, their transition from one state to another, and their movement from the nucleus to the cell membrane and back to the nucleus again. The model introduces stochastic variation into the system using a random generator within the Netlogo programming environment. The model uses these representations to understand the biological systems at three levels: individual cell fate, the interactions between cells, and the formation of pattern across the system. Using a set of assessment tools, we show that the current model accurately reproduces the rosette pattern of neurons and skin cells in the system over a wide set of parameters. Oscillations in the level of the N agent eventually stabilize cell fate into this pattern. We found that the dynamic timing and the availability of the N and Dl agents in neighboring cells are central to the formation of a correct and stable pattern. A feedback loop to the production of both components is necessary for a correct and stable pattern. CONCLUSIONS: The signaling pathways within and between cells in our model interact in real time to create a spatially correct field of neurons and skin cells. This model predicts that cells with high N and low Dl drive the formation of the pattern. This model also be used to elucidate general rules of biological self-patterning and decision-making. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12918-018-0672-9) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6332573 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-63325732019-01-16 An agent-based model of the Notch signaling pathway elucidates three levels of complexity in the determination of developmental patterning Reynolds, Elaine R. Himmelwright, Ryan Sanginiti, Christopher Pfaffmann, Jeffrey O. BMC Syst Biol Research Article BACKGROUND: The Notch signaling pathway is involved in cell fate decision and developmental patterning in diverse organisms. A receptor molecule, Notch (N), and a ligand molecule (in this case Delta or Dl) are the central molecules in this pathway. In early Drosophila embryos, these molecules determine neural vs. skin fates in a reproducible rosette pattern. RESULTS: We have created an agent-based model (ABM) that simulates the molecular components for this signaling pathway as agents acting within a spatial representation of a cell. The model captures the changing levels of these components, their transition from one state to another, and their movement from the nucleus to the cell membrane and back to the nucleus again. The model introduces stochastic variation into the system using a random generator within the Netlogo programming environment. The model uses these representations to understand the biological systems at three levels: individual cell fate, the interactions between cells, and the formation of pattern across the system. Using a set of assessment tools, we show that the current model accurately reproduces the rosette pattern of neurons and skin cells in the system over a wide set of parameters. Oscillations in the level of the N agent eventually stabilize cell fate into this pattern. We found that the dynamic timing and the availability of the N and Dl agents in neighboring cells are central to the formation of a correct and stable pattern. A feedback loop to the production of both components is necessary for a correct and stable pattern. CONCLUSIONS: The signaling pathways within and between cells in our model interact in real time to create a spatially correct field of neurons and skin cells. This model predicts that cells with high N and low Dl drive the formation of the pattern. This model also be used to elucidate general rules of biological self-patterning and decision-making. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12918-018-0672-9) contains supplementary material, which is available to authorized users. BioMed Central 2019-01-14 /pmc/articles/PMC6332573/ /pubmed/30642357 http://dx.doi.org/10.1186/s12918-018-0672-9 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Reynolds, Elaine R. Himmelwright, Ryan Sanginiti, Christopher Pfaffmann, Jeffrey O. An agent-based model of the Notch signaling pathway elucidates three levels of complexity in the determination of developmental patterning |
title | An agent-based model of the Notch signaling pathway elucidates three levels of complexity in the determination of developmental patterning |
title_full | An agent-based model of the Notch signaling pathway elucidates three levels of complexity in the determination of developmental patterning |
title_fullStr | An agent-based model of the Notch signaling pathway elucidates three levels of complexity in the determination of developmental patterning |
title_full_unstemmed | An agent-based model of the Notch signaling pathway elucidates three levels of complexity in the determination of developmental patterning |
title_short | An agent-based model of the Notch signaling pathway elucidates three levels of complexity in the determination of developmental patterning |
title_sort | agent-based model of the notch signaling pathway elucidates three levels of complexity in the determination of developmental patterning |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6332573/ https://www.ncbi.nlm.nih.gov/pubmed/30642357 http://dx.doi.org/10.1186/s12918-018-0672-9 |
work_keys_str_mv | AT reynoldselainer anagentbasedmodelofthenotchsignalingpathwayelucidatesthreelevelsofcomplexityinthedeterminationofdevelopmentalpatterning AT himmelwrightryan anagentbasedmodelofthenotchsignalingpathwayelucidatesthreelevelsofcomplexityinthedeterminationofdevelopmentalpatterning AT sanginitichristopher anagentbasedmodelofthenotchsignalingpathwayelucidatesthreelevelsofcomplexityinthedeterminationofdevelopmentalpatterning AT pfaffmannjeffreyo anagentbasedmodelofthenotchsignalingpathwayelucidatesthreelevelsofcomplexityinthedeterminationofdevelopmentalpatterning AT reynoldselainer agentbasedmodelofthenotchsignalingpathwayelucidatesthreelevelsofcomplexityinthedeterminationofdevelopmentalpatterning AT himmelwrightryan agentbasedmodelofthenotchsignalingpathwayelucidatesthreelevelsofcomplexityinthedeterminationofdevelopmentalpatterning AT sanginitichristopher agentbasedmodelofthenotchsignalingpathwayelucidatesthreelevelsofcomplexityinthedeterminationofdevelopmentalpatterning AT pfaffmannjeffreyo agentbasedmodelofthenotchsignalingpathwayelucidatesthreelevelsofcomplexityinthedeterminationofdevelopmentalpatterning |