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本文引用的文献

1
Chemokine signaling in embryonic cell migration: a fisheye view.胚胎细胞迁移中的趋化因子信号传导:鱼眼视角
Development. 2009 Apr;136(8):1223-9. doi: 10.1242/dev.022418.
2
Chemokine signaling controls endodermal migration during zebrafish gastrulation.趋化因子信号传导在斑马鱼原肠胚形成过程中控制内胚层迁移。
Science. 2008 Oct 3;322(5898):89-92. doi: 10.1126/science.1160038. Epub 2008 Aug 21.
3
Sdf1/Cxcr4 signaling controls the dorsal migration of endodermal cells during zebrafish gastrulation.Sdf1/Cxcr4信号通路在斑马鱼原肠胚形成过程中控制内胚层细胞的背侧迁移。
Development. 2008 Aug;135(15):2521-9. doi: 10.1242/dev.020107. Epub 2008 Jun 25.
4
Targeted gene inactivation in zebrafish using engineered zinc-finger nucleases.利用工程化锌指核酸酶在斑马鱼中进行靶向基因失活。
Nat Biotechnol. 2008 Jun;26(6):695-701. doi: 10.1038/nbt1398. Epub 2008 May 25.
5
Intra-endodermal interactions are required for pancreatic beta cell induction.胰腺β细胞诱导需要内胚层内相互作用。
Dev Cell. 2008 Apr;14(4):582-93. doi: 10.1016/j.devcel.2008.02.012.
6
Redundant roles of Sox17 and Sox18 in early cardiovascular development of mouse embryos.Sox17和Sox18在小鼠胚胎早期心血管发育中的冗余作用。
Biochem Biophys Res Commun. 2007 Aug 31;360(3):539-44. doi: 10.1016/j.bbrc.2007.06.093. Epub 2007 Jun 25.
7
Cxcl12/Cxcr4 chemokine signaling is required for placode assembly and sensory axon pathfinding in the zebrafish olfactory system.Cxcl12/Cxcr4趋化因子信号传导对于斑马鱼嗅觉系统中的基板组装和感觉轴突寻路是必需的。
Development. 2007 Jul;134(13):2459-68. doi: 10.1242/dev.001958. Epub 2007 May 30.
8
FoxH1 negatively modulates flk1 gene expression and vascular formation in zebrafish.FoxH1对斑马鱼中flk1基因的表达和血管形成起负向调节作用。
Dev Biol. 2007 Apr 15;304(2):735-44. doi: 10.1016/j.ydbio.2007.01.023. Epub 2007 Jan 20.
9
Whole-somite rotation generates muscle progenitor cell compartments in the developing zebrafish embryo.全体节旋转在发育中的斑马鱼胚胎中产生肌肉祖细胞区室。
Dev Cell. 2007 Feb;12(2):207-19. doi: 10.1016/j.devcel.2007.01.001.
10
Notch signalling limits angiogenic cell behaviour in developing zebrafish arteries.Notch信号通路限制斑马鱼发育中动脉血管生成细胞的行为。
Nature. 2007 Feb 15;445(7129):781-4. doi: 10.1038/nature05577. Epub 2007 Jan 28.

趋化因子信号传导引导胚胎第一条动脉的区域模式形成。

Chemokine signaling guides regional patterning of the first embryonic artery.

作者信息

Siekmann Arndt F, Standley Clive, Fogarty Kevin E, Wolfe Scot A, Lawson Nathan D

机构信息

Program in Gene Function and Expression, University of Massachusetts Medical School, Worcester, Massachusetts 01602, USA.

出版信息

Genes Dev. 2009 Oct 1;23(19):2272-7. doi: 10.1101/gad.1813509.

DOI:10.1101/gad.1813509
PMID:19797767
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2758748/
Abstract

The aorta traverses the body, yet little is known about how it is patterned in different anatomical locations. Here, we show that the aorta develops from genetically distinct endothelial cells originating from diverse locations within the embryo. Furthermore, chemokine (C-X-C motif) receptor 4a (cxcr4a) is restricted to endothelial cells derived from anterior mesoderm, and is required specifically for formation of the lateral aortae. Cxcl12b, a cxcr4a ligand, is expressed in endoderm underlying the lateral aortae, and loss of cxcl12b phenocopies cxcr4a deficiency. These studies reveal unexpected endothelial diversity within the aorta that is necessary to facilitate its regional patterning by local cues.

摘要

主动脉贯穿全身,但对于其在不同解剖位置的形成模式却知之甚少。在此,我们表明主动脉由源自胚胎内不同位置的基因上不同的内皮细胞发育而来。此外,趋化因子(C-X-C基序)受体4a(cxcr4a)仅限于源自前中胚层的内皮细胞,并且是形成侧主动脉所特需的。Cxcl12b,一种cxcr4a配体,在侧主动脉下方的内胚层中表达,并且cxcl12b的缺失模拟了cxcr4a缺陷的表型。这些研究揭示了主动脉内意想不到的内皮细胞多样性,这对于通过局部信号促进其区域模式形成是必要的。