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首页> 外文期刊>Developmental biology >Analysis of talpid(3) and wild-type chicken embryos reveals roles for Hedgehog signalling in development of the limb bud vasculature
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Analysis of talpid(3) and wild-type chicken embryos reveals roles for Hedgehog signalling in development of the limb bud vasculature

机译:talpid(3)和野生型鸡胚胎的分析揭示了刺猬信号在肢芽脉管系统发育中的作用

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摘要

Chicken talpid(3) mutant embryos have a wide range of Hedgehog-signalling related defects and it is now known that the talpid(3) gene product encodes a novel protein essential for Hedgehog signalling which is required for both activator and repressor functions of Gli transcription factors (Davey, M.G., Paton, I.R., Yin, Y., Schmidt, M., Bangs, F.K., Monice, D.R., Gordon-Smith, T, Buxton, P., Stamataki, D., Tanaka, M., Munsterberg, A.E., Briscoe, J., Tickle, C., Burt, D.W. (2006). The chicken talpic(3 gene encodes a novel protein essential for Hedgehog signalling. Genes Dev 20 1365-77). Haemorrhaging, oedema and other severe vascular defects are a central aspect of the talpid3 phenotype (Ede, D.A. and Kelly, W.A (1964a). Developmental abnormalities in the head region of the talpid3 mutant fowl. J. Embryol. exp. Morp. 12:161-182) and, as Hedgehog (Hh) signalling has been implicated in every stage of development of the vascular system, the vascular defects seen in talpid(3) are also likely to be attributable to abnormal Hedgehog signalling. Gene expression of members of the VEGF and Angiopoietin families of angiogenic growth factors has been linked to haemorrhaging and oedema and we find widespread expression of VEGF-D, rigf and Ang2a in the talpid3 limb. Furthermore, ectopic expression of these genes in talpid(3) limbs points to regulation via Gli repression rather than activation. We monitored specification of vessel identity in talpid(3) limb vasculature by examining expression of artery-specific genes, Np1 and EphrinB2, and the vein-specific genes, Xp2a and Tie2. We show that there are supernumerary subclavian arteries in talpid(3) limb buds and abnormal expression of an artery-specific gene in the venous submarginal sinus, despite the direction of blood flow being normal. Furthermore, we show that Shh can induce Np1 expression but has no effect on Np2a. Finally, we demonstrate that induction of VEGF and Ang2a expression by Shh in normal limb buds is accompanied by vascular remodelling. Thus Hedgehog signalling has a pivotal role in the cascade of angiogenic events in a growing embryonic organ which is similar to that proposed in tumours. (c) 2006 Elsevier Inc. All rights reserved.
机译:鸡talpid(3)突变体胚胎具有与刺猬信号有关的各种缺陷,现在已知talpid(3)基因产物编码了一种刺猬信号必不可少的新型蛋白质,这是Gli转录的激活子和阻遏子功能所必需的因素(Davey,MG,Paton,IR,Yin,Y.,Schmidt,M.,Bangs,FK,Monice,DR,Gordon-Smith,T,Buxton,P.,Stamataki,D.,Tanaka,M.,Munsterberg ,AE,Briscoe,J.,Tickle,C.,Burt,DW(2006)。鸡talpic(3基因编码对Hedgehog信号传导至关重要的新蛋白质。GenesDev 20 1365-77)。出血,水肿和其他严重血管缺陷是talpid3表型的主要方面(Ede,DA和Kelly,WA(1964a)。talpid3突变禽的头部发育异常。J. Embryol。exp。Morp。12:161-182),以及刺猬(Hh)信号已牵涉到血管系统发育的每个阶段,在talpid(3)中见到的血管缺陷也很可能y可归因于异常的刺猬信号。血管生成生长因子的VEGF和血管生成素家族成员的基因表达与出血和水肿有关,我们发现在talpid3肢中广泛表达VEGF-D,rigf和Ang2a。此外,这些基因在talpid(3)肢中的异位表达指向通过Gli抑制而不是激活来进行调节。我们通过检查动脉特异性基因Np1和EphrinB2以及静脉特异性基因Xp2a和Tie2的表达,监测了talpid(3)肢体脉管系统中血管身份的规范。我们显示,尽管血流方向正常,但在talpid(3)肢芽中有多余的锁骨下动脉,并且在静脉下缘窦中有动脉特异性基因的异常表达。此外,我们表明Shh可以诱导Np1表达,但对Np2a没有影响。最后,我们证明了Shh在正常肢芽中对VEGF和Ang2a表达的诱导伴随着血管重塑。因此,刺猬信号在生长中的胚胎器官中的血管生成事件的级联中具有关键作用,这与肿瘤中提出的类似。 (c)2006 Elsevier Inc.保留所有权利。

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