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Biological characterization of angiopoietin‐3 and angiopoietin‐4
Author(s) -
Lee Hyuek Jong,
Cho Chung-Hyun,
Hwang Su-Jeong,
Choi Han-Ho,
Kim Kyung-Tae,
Ahn So Young,
Kim Ju-Hyun,
Oh Jong-Lark,
Lee Gyun Min,
Koh Gou Young
Publication year - 2004
Publication title -
the faseb journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.709
H-Index - 277
eISSN - 1530-6860
pISSN - 0892-6638
DOI - 10.1096/fj.03-1466com
Subject(s) - angiopoietin receptor , angiogenesis , in vivo , protein kinase b , phosphorylation , agonist , biology , receptor , endothelial stem cell , microbiology and biotechnology , pharmacology , chemistry , in vitro , cancer research , biochemistry
The angiopoietin (Ang) family of growth factors includes Ang1, Ang2, Ang3, and Ang4, all of which bind to the endothelial receptor tyrosine kinase Tie2. Ang3 (mouse) and Ang4 (human) are interspecies orthologs. In experiments with human endothelial cell lines, Ang3 was identified as an antagonist of Tie2 and Ang4 was identified as an agonist of Tie2. However, the biological roles of Ang3 and Ang4 are unknown. We examined the biological effect of recombinant Ang3 and Ang4 proteins in primary cultured endothelial cells and in vivo in mice. Recombinant Ang3 and Ang4 formed disulfide‐linked dimers. Ang4 (400 ng/mL) markedly increased Tie2 and Akt phosphorylation in primary cultured HUVECs whereas Ang3 (400 ng/mL) did not produce significant changes. Accordingly, Ang4, but not Ang3, induced survival and migration in primary cultured HUVECs. Unexpectedly, intravenously administered Ang3 (30 µg) was more potent than Ang4 (30 µg) in phosphorylating the Tie2 receptor in lung tissue from mice in vivo. Accordingly, Ang3 was more potent than Ang4 in phosphorylating Akt in primary cultured mouse lung microvascular endothelial cells. Ang3 and Ang4 both produced potent corneal angiogenesis extending from the limbus across the mouse cornea in vivo. Thus, Ang3 and Ang4 are agonists of Tie2, but mouse Ang3 has strong activity only on endothelial cells of its own species.—Lee, H. J., Cho, C.‐H., Hwang, S.‐J., Choi, H.‐H., Kim, K.‐T., Ahn, S. Y., Kim, J.‐H., Oh, J.‐L., Lee, G. M., Koh, G. Y. Biological characterization of angiopoietin‐3 and angiopoietin‐4. FASEB J . 18, 1200–1208 (2004)