Biomimetic model to reconstitute angiogenic sprouting morphogenesis in vitro

Duc Huy T. Nguyen, Sarah C. Stapleton, Michael T. Yang, Susie S. Cha, Colin K. Choi, Peter A. Galie, Christopher S. Chen

Research output: Contribution to journalArticlepeer-review

263 Scopus citations

Abstract

Angiogenesis is a complex morphogenetic process whereby endo-thelial cells from existing vessels invade as multicellular sprouts to form new vessels. Here, we have engineered a unique organotypic model of angiogenic sprouting and neovessel formation that originates from preformed artificial vessels fully encapsulated within a 3D extracellular matrix. Using this model, we screened the effects of angiogenic factors and identified two distinct cocktails that promoted robust multicellular endothelial sprouting. The angiogenic sproutsinour system exhibited hallmark structural featuresofin vivo angiogenesis, including directed invasion of leading cells that developed filopodia-like protrusions characteristic of tip cells, following stalk cells exhibiting apical-basal polarity, and lumens and branches connecting back to the parent vessels. Ultimately, sprouts bridged between preformed channels and formed perfusable neovessels. Using this model, we investigated the effects of angiogenic inhibitors on sprouting morphogenesis. Interestingly, the ability of VEGF receptor 2 inhibition to antagonize filopodia formation in tip cells was context-dependent, suggesting a mechanism by which vessels might be able to toggle between VEGF-dependent and VEGF-independent modes of angiogenesis. Like VEGF, sphingosine-1-phosphate also seemed to exert its proangiogenic effects by stimulating directional filopodial extension, whereas matrix metal-loproteinase inhibitors prevented sprout extension but had no im-pactonfilopodial formation.Together, these resultsdemonstrate an in vitro 3D biomimetic model that reconstitutes the morphogenetic steps of angiogenic sprouting and highlight the potential utility of the model to elucidate the molecular mechanisms that coordinate the complex series of events involved in neovascularization.

Original languageEnglish (US)
Pages (from-to)6712-6717
Number of pages6
JournalProceedings of the National Academy of Sciences of the United States of America
Volume110
Issue number17
DOIs
StatePublished - Apr 23 2013

All Science Journal Classification (ASJC) codes

  • General

Fingerprint Dive into the research topics of 'Biomimetic model to reconstitute angiogenic sprouting morphogenesis in vitro'. Together they form a unique fingerprint.

Cite this