BioDiscovery (Sep 2012)

The Apoe-/- Mouse PhysioLab® Platform: A Validated Physiologically-based Mathematical Model of Atherosclerotic Plaque Progression in the Apoe-/- Mouse

  • Jason R Chan,
  • Gregory Vuillaume,
  • Caitlin Bever,
  • Stefan Lebrun,
  • Michael Lietz,
  • Yvonne Steffen,
  • Katrin Stolle,
  • Karim Wahba,
  • Xiao Wang,
  • Shonna Moodie,
  • Julia Hoeng,
  • Manuel C Peitsch,
  • Lyn M Powell

DOI
https://doi.org/10.7750/BioDiscovery.2012.3.2
Journal volume & issue
Vol. 3
pp. 1 – 13

Abstract

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<em>Motivation:</em>Atherosclerosis is a complex multi-pathway inflammatory disease where accumulation of oxidatively modified lipids and leukocytes in the arterial intima leads to plaque formation over time. Translating Apoe<sup>-/-</sup> mouse results to the clinical setting is complicated by uncertainty around (a) mechanisms underlying disease etiology, (b) relative importance of these mechanisms as drivers of progression, and (c) how these roles change in response to perturbation by therapeutic intervention or lifestyle changes. <br><em>Results: </em>We describe a large-scale mechanistic, mathematical model of atherosclerosis in the Apoe<sup>-/-</sup> mouse and its validation with <em>in vivo</em> Apoe <sup>-/-</sup> data. Major physiological components include cholesterol/macrophage trafficking, inflammation, endothelial function, oxidative stress, and thrombosis. Heterogeneity in disease progression, observed despite genetic uniformity and experimentally controlled conditions, was captured through “virtual mice”. This model may be used to optimize <em>in vivo</em> experiments and paves the way for a similar modeling approach for human disease.<br><em>Availability: </em>The model is available by remote desktop client at Apoe.entelos.com.

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