Literature DB >> 11861480

Patterning of angiogenesis in the zebrafish embryo.

Sarah Childs1, Jau-Nian Chen, Deborah M Garrity, Mark C Fishman.   

Abstract

Little is known about how vascular patterns are generated in the embryo. The vasculature of the zebrafish trunk has an extremely regular pattern. One intersegmental vessel (ISV) sprouts from the aorta, runs between each pair of somites, and connects to the dorsal longitudinal anastomotic vessel (DLAV). We now define the cellular origins, migratory paths and cell fates that generate these metameric vessels of the trunk. Additionally, by a genetic screen we define one gene, out of bounds (obd), that constrains this angiogenic growth to a specific path. We have performed lineage analysis, using laser activation of a caged dye and mosaic construction to determine the origin of cells that constitute the ISV. Individual angioblasts destined for the ISVs arise from the lateral posterior mesoderm (LPM), and migrate to the dorsal aorta, from where they migrate between somites to their final position in the ISVs and dorsal longitudinal anastomotic vessel (DLAV). Cells of each ISV leave the aorta only between the ventral regions of two adjacent somites, and migrate dorsally to assume one of three ISV cell fates. Most dorsal is a T-shaped cell, based in the DLAV and branching ventrally; the second constitutes a connecting cell; and the third an inverted T-shaped cell, based in the aorta and branching dorsally. The ISV remains between somites during its ventral course, but changes to run mid-somite dorsally. This suggests that the pattern of ISV growth ventrally and dorsally is guided by different cues. We have also performed an ENU mutagenesis screen of 750 mutagenized genomes and identified one mutation, obd that disrupts this pattern. In obd mutant embryos, ISVs sprout precociously at abnormal sites and migrate anomalously in the vicinity of ventral somite. The dorsal extent of the ISV is less perturbed. Precocious sprouting can be inhibited in a VEGF morphant, but the anomalous site of origin of obd ISVs remains. In mosaic embryos, obd somite causes adjacent wild-type endothelial cells to assume the anomalous ISV pattern of obd embryos. Thus, the launching position of the new sprout and its initial trajectory are directed by inhibitory signals from ventral somites. Zebrafish ISVs are a tractable system for defining the origins and fates of vessels, and for dissecting elements that govern patterns of vessel growth.

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Mesh:

Year:  2002        PMID: 11861480     DOI: 10.1242/dev.129.4.973

Source DB:  PubMed          Journal:  Development        ISSN: 0950-1991            Impact factor:   6.868


  96 in total

1.  Angiomotin-like2 gene (amotl2) is required for migration and proliferation of endothelial cells during angiogenesis.

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Review 2.  Fishing for novel angiogenic therapies.

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Review 3.  Current methods for assaying angiogenesis in vitro and in vivo.

Authors:  Carolyn A Staton; Stephen M Stribbling; Simon Tazzyman; Russell Hughes; Nicola J Brown; Claire E Lewis
Journal:  Int J Exp Pathol       Date:  2004-10       Impact factor: 1.925

Review 4.  How blood vessel networks are made and measured.

Authors:  John C Chappell; David M Wiley; Victoria L Bautch
Journal:  Cells Tissues Organs       Date:  2011-10-12       Impact factor: 2.481

5.  Non-core subunit eIF3h of translation initiation factor eIF3 regulates zebrafish embryonic development.

Authors:  Avik Choudhuri; Todd Evans; Umadas Maitra
Journal:  Dev Dyn       Date:  2010-06       Impact factor: 3.780

6.  Patterning mechanisms of the sub-intestinal venous plexus in zebrafish.

Authors:  Michela Goi; Sarah J Childs
Journal:  Dev Biol       Date:  2015-10-22       Impact factor: 3.582

7.  Selective disruption of vascular endothelium of zebrafish embryos by ultrafast laser microsurgical treatment.

Authors:  Suk-Yi Woo; Heh-Young Moon; Tag Gyum Kim; Heung Soon Lee; Mehra S Sidhu; Changho Kim; Jae-Phil Jeon; Sae Chae Jeoung
Journal:  Biomed Opt Express       Date:  2015-11-04       Impact factor: 3.732

8.  PlexinD1 is required for proper patterning of the periocular vascular network and for the establishment of corneal avascularity during avian ocular development.

Authors:  Sam C Kwiatkowski; Ana F Ojeda; Peter Y Lwigale
Journal:  Dev Biol       Date:  2016-01-16       Impact factor: 3.582

9.  Branching morphogenesis.

Authors:  Arie Horowitz; Michael Simons
Journal:  Circ Res       Date:  2009-01-30       Impact factor: 17.367

10.  GIPC proteins negatively modulate Plexind1 signaling during vascular development.

Authors:  Jorge Carretero-Ortega; Zinal Chhangawala; Shane Hunt; Carlos Narvaez; Javier Menéndez-González; Carl M Gay; Tomasz Zygmunt; Xiaochun Li; Jesús Torres-Vázquez
Journal:  Elife       Date:  2019-05-03       Impact factor: 8.140

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