Integration of angiogenesis modules at multiple scales: from molecular to tissue

Pac Symp Biocomput. 2009:316-27.

Abstract

Multiscale modeling has emerged as a powerful approach to interpret and capitalize on the biological complexity underlying blood vessel growth. We present a multiscale model of angiogenesis that heralds the start of a large scale initiative to integrate related biological models. The goal of the integrative project is to better understand underlying biological mechanisms from the molecular level up through the organ systems level, and test new therapeutic strategies. Model methodology includes ordinary and partial differential equations, stochastic models, complex logical rules, and agent-based architectures. Current modules represent blood flow, oxygen transport, growth factor distribution and signaling, cell sensing, cell movement and cell proliferation. Challenges of integration lie in connecting modules that are diversely designed, seamlessly coordinating feedback, and representing spatial and time scales from ligand-receptor interactions and intracellular signaling, to cell-level movement and cell-matrix interactions, to vessel branching and capillary network formation, to tissue level characteristics, to organ system response. We briefly introduce the individual modules, discuss our approach to integration, present initial results from the coordination of modules, and propose solutions to some critical issues facing angiogenesis multiscale modeling and integration.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Biomedical Engineering
  • Biometry
  • Humans
  • Hypoxia / pathology
  • Matrix Metalloproteinases / physiology
  • Models, Cardiovascular*
  • Muscle, Skeletal / blood supply
  • Neovascularization, Pathologic
  • Neovascularization, Physiologic*
  • Oxygen Consumption
  • Regional Blood Flow
  • Vascular Endothelial Growth Factor A / physiology

Substances

  • Vascular Endothelial Growth Factor A
  • Matrix Metalloproteinases