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December 1, 1985The Journal of Cell Biology280 citationsOpen Access

Human endothelial cells are chemotactic to endothelial cell growth factor and heparin.

VTVictor P. TerranovaRDRoberta M. diFlorio‐AlexanderRLRaymond M. Lyall

Key Points

  • To evaluate the migratory responses of human endothelial cells to various growth factors and extracellular matrix components, specifically focusing on endothelial cell growth factor and heparin.
  • Assessed human endothelial cell migration (chemotaxis and chemokinesis) using a modified Boyden chamber assay.
  • Tested endothelial cell responses to endothelial cell growth factor (10⁻⁹ M), anti-ECGF antibodies, heparin (10⁻⁸ to 10⁻¹⁰ M), collagens (types I–V), fibronectin, laminin, and other polypeptide growth factors.
  • Endothelial cell growth factor (10⁻⁹ M) increased endothelial cell chemotaxis and chemokinesis, which was specifically inhibited by anti-ECGF antibody.
  • Heparin (10⁻⁸ to 10⁻¹⁰ M) stimulated chemotaxis independently and potentiated the chemotactic response induced by ECGF.
  • Laminin, fibronectin, collagens I–V, and epidermal, fibroblast, and nerve growth factors induced chemotactic activity that was one-third to one-half less than that observed with ECGF.

Abstract

The response of human endothelial cell migration to various extracellular matrix components and growth factors has been assessed. Human endothelial cells demonstrate increased chemotaxis and chemokinesis when placed in a modified Boyden chamber with endothelial cell growth factor (ECGF) used at a concentration of 10(-9) M. Anti-ECGF antibody inhibits the chemotactic response. Heparin (10(-8) to 10(-10) M) was also chemotactic and was shown to potentiate the chemotactic activity of ECGF. Although laminin, fibronectin, the polypeptide (epidermal, fibroblast, and nerve) growth factors, and collagen types I, II, III, IV, and V demonstrate a chemotactic response, these activities were one third to one half less than observed with ECGF. These data suggest that ECGF and heparin may play a significant role as response modifiers of human endothelial cell migration which may be relevant to tumor metastasis, wound healing, and atherogenesis.

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Cite This Study

Terranova et al. (1985) studied this question.

synapsesocial.com/papers/6a0cd27ba4d785ea81625fe5https://doi.org/10.1083/jcb.101.6.2330
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Also Consider

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