help button home button Biophys. J.
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH

Biophys. J. BioFAST: First Published June 27, 2008. doi:10.1529/biophysj.107.124511
© 2008 by the Biophysical Society.


A more recent version of this article appeared on October 1, 2008.
This Article
Right arrow Full Text (Rapid PDF)
Right arrow Supplement
Right arrow All Versions of this Article:
biophysj.107.124511v1
95/7/3146    most recent
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Google Scholar
Right arrow Articles by Milde, F.
Right arrow Articles by Koumoutsakos, P.
PubMed
Right arrow PubMed Citation
Right arrow Articles by Milde, F.
Right arrow Articles by Koumoutsakos, P.

BIOPHYSICAL THEORY AND MODELING

A Hybrid Model for 3D Simulations of Sprouting Angiogenesis

Florian Milde 1, Michael Bergdorf 1 and Petros Koumoutsakos 1*

1 ETH Zurich

* To whom correspondence should be addressed. E-mail: petros{at}ethz.ch.

Submitted on October 29, 2007
Revised on December 17, 2007
Accepted on 23 May 2008


   Abstract
Recent advances in cancer research have identified critical angiogenic signaling pathways and the influence of the extracellular matrix on endothelial cell migration. These findings provide us with insight into the process of angiogenesis that can facilitate the development of effective computational models of sprouting angiogenesis. In this work, we present the first 3D model of sprouting angiogenesis that consider explicitly the effect of the extracellular matrix and of the soluble as well as matrix bound growth factors on capillary growth. The computational model relies on a hybrid particle-mesh representation of the blood vessels and it introduces an implicit representation of the vasculature that can accommodate detailed descriptions of nutrient transport. Extensive parametric studies reveal the role of the extracellular matrix structure and the distribution of the different VEGF isoforms on the dynamics and the morphology of the generated vascular networks.

Key Words: ECM, VEGF, angiogenesis, cancer, particle methods







HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH
Copyright © 2008 by the Biophysical Society.