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本文引用的文献

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Suppression of Notch signalling by the COUP-TFII transcription factor regulates vein identity.COUP-TFII转录因子对Notch信号通路的抑制作用调控静脉特性。
Nature. 2005 May 5;435(7038):98-104. doi: 10.1038/nature03511.
2
Vegfc is required for vascular development and endoderm morphogenesis in zebrafish.Vegfc是斑马鱼血管发育和内胚层形态发生所必需的。
EMBO Rep. 2004 Jan;5(1):78-84. doi: 10.1038/sj.embor.7400047.
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Zebrafish angiogenesis: a new model for drug screening.斑马鱼血管生成:一种药物筛选的新模型。
Angiogenesis. 1999;3(4):353-9. doi: 10.1023/a:1026598300052.
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Angiogenic network formation in the developing vertebrate trunk.发育中的脊椎动物躯干中的血管生成网络形成。
Development. 2003 Nov;130(21):5281-90. doi: 10.1242/dev.00733. Epub 2003 Sep 3.
5
Ligand-induced vascular endothelial growth factor receptor-3 (VEGFR-3) heterodimerization with VEGFR-2 in primary lymphatic endothelial cells regulates tyrosine phosphorylation sites.配体诱导的原发性淋巴管内皮细胞中血管内皮生长因子受体-3(VEGFR-3)与VEGFR-2异源二聚化可调节酪氨酸磷酸化位点。
J Biol Chem. 2003 Oct 17;278(42):40973-9. doi: 10.1074/jbc.M304499200. Epub 2003 Jul 24.
6
Role of PlGF in the intra- and intermolecular cross talk between the VEGF receptors Flt1 and Flk1.胎盘生长因子(PlGF)在血管内皮生长因子(VEGF)受体Flt1和Flk1的分子内及分子间相互作用中的作用
Nat Med. 2003 Jul;9(7):936-43. doi: 10.1038/nm884.
7
phospholipase C gamma-1 is required downstream of vascular endothelial growth factor during arterial development.磷脂酶Cγ-1在动脉发育过程中是血管内皮生长因子下游所必需的。
Genes Dev. 2003 Jun 1;17(11):1346-51. doi: 10.1101/gad.1072203.
8
The biology of VEGF and its receptors.血管内皮生长因子(VEGF)及其受体的生物学特性
Nat Med. 2003 Jun;9(6):669-76. doi: 10.1038/nm0603-669.
9
Regulation of vascular permeability by vascular endothelial growth factors.血管内皮生长因子对血管通透性的调节
Vascul Pharmacol. 2002 Nov;39(4-5):225-37. doi: 10.1016/s1537-1891(03)00011-9.
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Modulation of VEGFR-2-mediated endothelial-cell activity by VEGF-C/VEGFR-3.VEGF-C/VEGFR-3对VEGFR-2介导的内皮细胞活性的调节
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斑马鱼中不同类型血管的发育需要多种Vegf受体之间独特的基因相互作用。

Distinct genetic interactions between multiple Vegf receptors are required for development of different blood vessel types in zebrafish.

作者信息

Covassin L D, Villefranc J A, Kacergis M C, Weinstein B M, Lawson N D

机构信息

Program in Gene Function and Expression, University of Massachusetts Medical School, Worcester, MA 01605, USA.

出版信息

Proc Natl Acad Sci U S A. 2006 Apr 25;103(17):6554-9. doi: 10.1073/pnas.0506886103. Epub 2006 Apr 14.

DOI:10.1073/pnas.0506886103
PMID:16617120
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1458922/
Abstract

Recent evidence indicates a specific role for vascular endothelial growth factor a (Vegfa) during artery development in both zebrafish and mouse embryos, whereas less is known about signals that govern vein formation. In zebrafish, loss of vegfa blocks segmental artery formation and reduces artery-specific gene expression, whereas veins are largely unaffected. Here, we describe a mutation in the zebrafish vegf receptor-2 homolog, kdra, which eliminates its kinase activity and leads to specific defects in artery development. We further find that Flt4, a receptor for Vegfc, cooperates with Kdr during artery morphogenesis, but not differentiation. We also identify an additional zebrafish vegfr-2 ortholog, referred to as kdrb, which can partially compensate for loss of kdra but is dispensable for vascular development in wild-type embryos. Interestingly, we find that these Vegf receptors are also required for formation of veins but in distinct genetic interactions that differ from those required for artery development. Taken together, our results indicate that formation of arteries and veins in the embryo is governed in part by different Vegf receptor combinations and suggest a genetic mechanism for generating blood vessel diversity during vertebrate development.

摘要

最近的证据表明,血管内皮生长因子a(Vegfa)在斑马鱼和小鼠胚胎的动脉发育过程中具有特定作用,而对于调控静脉形成的信号了解较少。在斑马鱼中,Vegfa的缺失会阻碍节段性动脉的形成并降低动脉特异性基因的表达,而静脉基本不受影响。在此,我们描述了斑马鱼Vegf受体-2同源物kdra中的一种突变,该突变消除了其激酶活性并导致动脉发育出现特定缺陷。我们进一步发现,Vegfc的受体Flt4在动脉形态发生过程中与Kdr协同作用,但在分化过程中并非如此。我们还鉴定出另一种斑马鱼Vegfr-2直系同源物,称为kdrb,它可以部分补偿kdra的缺失,但对于野生型胚胎的血管发育并非必需。有趣的是,我们发现这些Vegf受体对于静脉形成也是必需的,但在不同的遗传相互作用中,这些相互作用与动脉发育所需的相互作用不同。综上所述,我们的结果表明,胚胎中动脉和静脉的形成部分受不同的Vegf受体组合调控,并提示了一种在脊椎动物发育过程中产生血管多样性的遗传机制。