TY - JOUR
T1 - Angiogenesis inhibition by transdominant mutant Ets-1
AU - Nakano, Toru
AU - Abe, Mayumi
AU - Tanaka, Katsuhiro
AU - Shineha, Ryuzaburo
AU - Satomi, Susumu
AU - Sato, Yasufumi
PY - 2000
Y1 - 2000
N2 - The expression of transcription factor Ets-1 is induced in endothelial cells (ECs) by angiogenic factor; and in turn Ets-1 converts ECs to angiogenic invasive phenotype. In order to control angiogenesis, we constructed a transdominant mutant Ets-1 (TMEts-1) which acts as a dominant negative molecule. This molecule inhibited the DNA binding and the transactivation activity of the wild-type Ets-1. Stable transfection of murine endothelial cell line MSS31 cells with the TMets-1 gene impaired angiogenic activities including proliferation, migration, invasion, and tube formation in type-1 collagen gel. Finally, we incorporated the TMets-1 gene into a non-proliferative adenovirus vector, designated as AdTMets-1. AdTMets- 1 significantly inhibited angiogenesis in the Matrigel plugs injected into the subcutaneous tissue of C57BL mice. These results indicate that TMets-1 would be a tool for angiogenic inhibition. (C) 2000 Wiley-Liss, Inc.
AB - The expression of transcription factor Ets-1 is induced in endothelial cells (ECs) by angiogenic factor; and in turn Ets-1 converts ECs to angiogenic invasive phenotype. In order to control angiogenesis, we constructed a transdominant mutant Ets-1 (TMEts-1) which acts as a dominant negative molecule. This molecule inhibited the DNA binding and the transactivation activity of the wild-type Ets-1. Stable transfection of murine endothelial cell line MSS31 cells with the TMets-1 gene impaired angiogenic activities including proliferation, migration, invasion, and tube formation in type-1 collagen gel. Finally, we incorporated the TMets-1 gene into a non-proliferative adenovirus vector, designated as AdTMets-1. AdTMets- 1 significantly inhibited angiogenesis in the Matrigel plugs injected into the subcutaneous tissue of C57BL mice. These results indicate that TMets-1 would be a tool for angiogenic inhibition. (C) 2000 Wiley-Liss, Inc.
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U2 - 10.1002/1097-4652(200008)184:2<255::AID-JCP14>3.0.CO;2-J
DO - 10.1002/1097-4652(200008)184:2<255::AID-JCP14>3.0.CO;2-J
M3 - Article
C2 - 10867651
AN - SCOPUS:0033949087
SN - 0021-9541
VL - 184
SP - 255
EP - 262
JO - Journal of Cellular Physiology
JF - Journal of Cellular Physiology
IS - 2
ER -