Properties of two VEGF receptors, Flt-1 and KDR, in signal transduction

被引:0
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作者
Sato, Y [1 ]
Kanno, S
Oda, N
Abe, M
Ito, M
Shitara, K
Shibuya, M
机构
[1] Tohoku Univ, Inst Dev Aging & Canc, Dept Vasc Biol, Sendai, Miyagi 9808575, Japan
[2] Kyowa Hakko Kogyo Co Ltd, Tokyo Res Labs, Machida, Tokyo, Japan
[3] Univ Tokyo, Inst Med Sci, Dept Genet, Tokyo, Japan
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中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The properties of two VEGF receptors, Flt-1 and KDR, in the signal transduction of VEGF in human umbilical vein endothelial cells (HUVECs) were investigated by using two newly developed blocking monoclonal antibodies (mAbs) against Flt-1 and KDR, VEGF stimulated the expression of transcription factor Ets-l as well as matrix metalloproteinase-l (MMP-1) and Flt-1 in HUVECs. The KDR/Flt-1 heterodimer and the KDR homodimer mediate the expression of Ets-l, MMP-1, and Flt-1. VEGF also stimulated DNA synthesis and migration of HUVECs. DNA synthesis is mediated by the same signaling system as the expression of Ets-l, In contrast, cell migration is regulated by two distinct signaling systems. The Flt-1 homodimer is required for actin reorganization. The KDR/Flt-1 heterodimer and the KDR homodimer are required for the assembly of vinculin in focal adhesion plaque by regulating the phosphorylation of focal adhesion kinase (FAK) and paxillin.
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页码:201 / 207
页数:7
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