Long-term and sustained COMP-Ang1 induces long-lasting vascular enlargement and enhanced blood flow

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Vascular enlargement is a characteristic feature of angiopoietin-1 (Ang1)-induced changes in adult blood vessels. However, it is unknown whether tissues having Ang1-mediated vascular enlargement have more blood flow or whether the enlargement is reversible. We have recently created a soluble, stable and potent Ang1 variant, COMP-Ang1. In the present study, we investigated the effects of varied dose and duration of COMP-Ang1 on vascular enlargement and blood flow in the tracheal microvasculature of adult mice and explored a possible mechanism of long-lasting vascular enlargement. We found that COMP-Ang1 administered by adenoviral vector induced long-lasting vascular enlargement and increased tracheal blood flow. In contrast, short-term administration of COMP-Ang1 recombinant protein induced transient vascular enlargement that spontaneously reversed within a month. In both cases, the vascular enlargement resulted from endothelial proliferation. The COMP-Ang1-induced vascular remodeling is mediated mainly through Tie2 activation. Sustained overexpression of Tie2 could participate in the maintenance of vascular changes. Together, our findings indicate that sustained treatment with COMP-Ang1 can produce long-lasting vascular enlargement and increased blood flow.
Publisher
LIPPINCOTT WILLIAMS & WILKINS
Issue Date
2005-07
Language
English
Article Type
Article
Keywords

RECEPTOR TYROSINE KINASE; ENDOTHELIAL GROWTH-FACTOR; DESIGNED ANGIOPOIETIN-1 VARIANT; TIE2 RECEPTOR; OVEREXPRESSING ANGIOPOIETIN-1; EXPRESSION; VESSELS; CELLS; MICE; LIGAND

Citation

CIRCULATION RESEARCH, v.97, no.1, pp.86 - 94

ISSN
0009-7330
DOI
10.1161/01.RES.0000174093.64855.a6
URI
http://hdl.handle.net/10203/92583
Appears in Collection
BS-Journal Papers(저널논문)MSE-Journal Papers(저널논문)
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