Transcription factor COUP-TFII is indispensable for venous and lymphatic development in zebrafish and Xenopus laevis

被引:39
|
作者
Aranguren, Xabier L. [1 ]
Beerens, Manu [1 ]
Vandevelde, Wouter [2 ,3 ]
Dewerchin, Mieke [2 ,3 ]
Carmeliet, Peter [2 ,3 ]
Luttun, Aernout [1 ]
机构
[1] Katholieke Univ Leuven, Ctr Mol & Vasc Biol, B-3000 Louvain, Belgium
[2] VIB, Vesalius Res Ctr, B-3000 Louvain, Belgium
[3] Katholieke Univ Leuven, Vesalius Res Ctr, B-3000 Louvain, Belgium
关键词
COUP-TFII; Endothelial specification; (Lymph)angiogenesis; Zebrafish; Xenopus laevis; Prox1; ENDOTHELIAL-CELLS; LYMPHANGIOGENESIS; VASCULATURE; PROX1; SPECIFICATION; EXPRESSION; UPSTREAM; NOTCH; SOX18;
D O I
10.1016/j.bbrc.2011.05.117
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Transcription factors play a central role in cell fate determination. Gene targeting in mice revealed that Chicken Ovalbumin Upstream Promoter-Transcription Factor II (COUP-TFII, also known as Nuclear Receptor 2F2 or NR2F2) induces a venous phenotype in endothelial cells (ECs). More recently, NR2F2 was shown to be required for initiating the expression of Prox1, responsible for lymphatic commitment of venous ECs. Small animal models like zebrafish embryos and Xeno pus laevis tadpoles have been very useful to elucidate mechanisms of (lymph) vascular development. Therefore, the role of NR2F2 in (lymph) vascular development was studied by eliminating its expression in these models. Like in mice, absence of NR2F2 in zebrafish resulted in distinct vascular defects including loss of venous marker expression, major trunk vessel fusion and vascular leakage. Both in zebrafish and Xenopus the development of the main lymphatic structures was severely hampered. NR2F2 knockdown significantly decreased prox1 expression in zebrafish ECs and the same manipulation affected lymphatic (L)EC commitment, migration and function in Xenopus tadpoles. Therefore, the role of NR2F2 in EC fate determination is evolutionary conserved. (C) 2011 Elsevier Inc. All rights reserved.
引用
收藏
页码:121 / 126
页数:6
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