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Cited by 370

The DOI matches its Crossref record; 2 of the 2 references it cites were found in a registry or an index.

Angiopoietin-1 Reduces VEGF-Stimulated Leukocyte Adhesion to Endothelial Cells by Reducing ICAM-1, VCAM-1, and E-Selectin Expression

Open access
Kim, Injune, Moon, Sang-Ok, Park, Sung Kwang, Chae, Soo Wan, Koh, Gou Young·2001·Circulation Research

Abstract

Vascular endothelial growth factor (VEGF) and angiopoietin-1 (Ang1) are potent vasculogenic and angiogenic factors that hold promise as a means to produce therapeutic vascularization and angiogenesis. However, VEGF also acts as a proinflammatory cytokine by inducing adhesion molecules that bind leukocytes to endothelial cells, an initial and essential step toward inflammation. In the present study, we used human umbilical vascular endothelial cells (HUVECs) to examine the effect of Ang1 on VEGF-induced expression of three adhesion molecules: intercellular adhesion molecule-1 (ICAM-1), vascular cell adhesion molecule-1 (VCAM-1), and E-selectin. Interestingly, Ang1 suppressed VEGF-induced expression of these adhesion molecules. Furthermore, Ang1 reduced VEGF-induced leukocyte adhesion to HUVECs. These results demonstrate that Ang1 counteracts VEGF-induced inflammation by reducing VEGF-induced endothelial adhesiveness.

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Metadata

Authors
Kim, I., Moon, S.-O., Park, S. K., Chae, S. W., & Koh, G. Y.
Venue
Circulation Research
Published
2001-09-14
Volume
89
Issue
6
Pages
477-479
ISSN
  • 0009-7330 (ISSN-L)
  • 1524-4571
OpenAlex
W2101831526
Cited by
370
References
2
FWCI
4.56
Type
journal article
Language
en
Open access
bronze

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CoChat. (2026). Citation check: Angiopoietin-1 Reduces VEGF-Stimulated Leukocyte Adhesion to Endothelial Cells by Reducing ICAM-1, VCAM-1, and E-Selectin Expression. https://app.cochat.ai/papers/10.1161/hh1801.097034
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Kim, I., Moon, S.-O., Park, S. K., Chae, S. W., & Koh, G. Y. (2001). Angiopoietin-1 Reduces VEGF-Stimulated Leukocyte Adhesion to Endothelial Cells by Reducing ICAM-1, VCAM-1, and E-Selectin Expression. Circulation Research. https://doi.org/10.1161/hh1801.097034

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