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Cold Spring Harb Perspect Med. 2012 May;2(5):a006684. doi: 10.1101/cshperspect.a006684.
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DDX24 spatiotemporally orchestrates VEGF and Wnt signaling during developmental angiogenesis.在发育性血管生成过程中,DDX24在时空上协调血管内皮生长因子(VEGF)和Wnt信号传导。
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本文引用的文献

1
Moesin1 and Ve-cadherin are required in endothelial cells during in vivo tubulogenesis.Moesin1 和 Ve-cadherin 在体内小管形成过程中内皮细胞中是必需的。
Development. 2010 Sep;137(18):3119-28. doi: 10.1242/dev.048785.
2
Hematopoietic development in the zebrafish.斑马鱼的造血发育
Int J Dev Biol. 2010;54(6-7):1127-37. doi: 10.1387/ijdb.093042ep.
3
Arteries provide essential guidance cues for lymphatic endothelial cells in the zebrafish trunk.动脉为斑马鱼躯干中的淋巴管内皮细胞提供必要的导向线索。
Development. 2010 Aug;137(16):2653-7. doi: 10.1242/dev.048207. Epub 2010 Jul 7.
4
Ephrin-B2 controls VEGF-induced angiogenesis and lymphangiogenesis.Ephrin-B2 控制 VEGF 诱导的血管生成和淋巴管生成。
Nature. 2010 May 27;465(7297):483-6. doi: 10.1038/nature09002.
5
ETS family protein ETV2 is required for initiation of the endothelial lineage but not the hematopoietic lineage in the Xenopus embryo.ETS 家族蛋白 ETV2 对于非洲爪蟾胚胎中内皮谱系的起始而不是造血谱系的起始是必需的。
Dev Dyn. 2010 Apr;239(4):1178-87. doi: 10.1002/dvdy.22277.
6
Lymphangiogenesis: Molecular mechanisms and future promise.淋巴管生成:分子机制与未来前景。
Cell. 2010 Feb 19;140(4):460-76. doi: 10.1016/j.cell.2010.01.045.
7
Mutations in CCBE1 cause generalized lymph vessel dysplasia in humans.CCBE1 基因突变导致人类全身性淋巴管发育不良。
Nat Genet. 2009 Dec;41(12):1272-4. doi: 10.1038/ng.484.
8
Selective inhibition of retinal angiogenesis by targeting PI3 kinase.靶向 PI3 激酶抑制视网膜血管生成。
PLoS One. 2009 Nov 17;4(11):e7867. doi: 10.1371/journal.pone.0007867.
9
Linkage and sequence analysis indicate that CCBE1 is mutated in recessively inherited generalised lymphatic dysplasia.连锁分析和序列分析表明 CCBE1 基因发生突变导致常染色体隐性遗传的全身性淋巴组织发育不良。
Hum Genet. 2010 Feb;127(2):231-41. doi: 10.1007/s00439-009-0766-y. Epub 2009 Nov 13.
10
The molecular basis of vascular lumen formation in the developing mouse aorta.发育中小鼠主动脉血管腔形成的分子基础。
Dev Cell. 2009 Oct;17(4):505-15. doi: 10.1016/j.devcel.2009.08.011.

斑马鱼的血管发育。

Vascular development in the zebrafish.

机构信息

Program in Genomics of Differentiation, Laboratory of Molecular Genetics, Section on Vertebrate Organogenesis, NICHD, NIH, Bethesda, Maryland, USA.

出版信息

Cold Spring Harb Perspect Med. 2012 May;2(5):a006684. doi: 10.1101/cshperspect.a006684.

DOI:10.1101/cshperspect.a006684
PMID:22553495
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3331685/
Abstract

The zebrafish has emerged as an excellent vertebrate model system for studying blood and lymphatic vascular development. The small size, external and rapid development, and optical transparency of zebrafish embryos are some of the advantages the zebrafish model system offers. Multiple well-established techniques have been developed for imaging and functionally manipulating vascular tissues in zebrafish embryos, expanding on and amplifying these basic advantages and accelerating use of this model system for studying vascular development. In the past decade, studies performed using zebrafish as a model system have provided many novel insights into vascular development. In this article we discuss the amenability of this model system for studying blood vessel development and review contributions made by this system to our understanding of vascular development.

摘要

斑马鱼已成为研究血液和淋巴血管发育的优秀脊椎动物模型系统。斑马鱼模型系统的优势包括其体型小、体外发育且发育迅速、胚胎光学透明等。目前已经开发出多种成熟的技术,可用于对斑马鱼胚胎中的血管组织进行成像和功能操作,进一步扩展和放大了这些基本优势,并加速了该模型系统在血管发育研究中的应用。在过去十年中,使用斑马鱼作为模型系统进行的研究为血管发育提供了许多新的见解。本文我们讨论了该模型系统在研究血管生成方面的适用性,并回顾了该系统对我们理解血管生成的贡献。