Please use this identifier to cite or link to this item:
https://doi.org/10.7554/eLife.06726
Title: | The hormonal peptide Elabela guides angiob lasts to the midline during vasculogenesis | Authors: | Helker, C.S.M Schuermann, A Pollmann, C Chng, S.C Kiefer, F Reversade, B Herzog, W |
Keywords: | apelin receptor chemoattractant elabela messenger RNA peptide hormone plasmid DNA sonic hedgehog protein unclassified drug vasculotropin A vasculotropin receptor 2 Apela protein, zebrafish apelin protein, zebrafish chemokine primer DNA zebrafish protein angiogenesis animal cell Article cell migration confocal microscopy controlled study embryo endothelium cell gene overexpression genetic code hemangioblast in situ hybridization microinjection mutation nonhuman notochord protein expression signal transduction time lapse imaging transplantation zebra fish angiogenesis animal biological model cell motion cytology endothelial progenitor cell genetics human metabolism molecular cloning mutagenesis physiology Danio rerio Animals Cell Movement Chemokines Cloning, Molecular DNA Primers Endothelial Cells Endothelial Progenitor Cells Humans In Situ Hybridization Models, Biological Mutagenesis Neovascularization, Physiologic Zebrafish Zebrafish Proteins |
Issue Date: | 2015 | Citation: | Helker, C.S.M, Schuermann, A, Pollmann, C, Chng, S.C, Kiefer, F, Reversade, B, Herzog, W (2015). The hormonal peptide Elabela guides angiob lasts to the midline during vasculogenesis. eLife 4 (MAY). ScholarBank@NUS Repository. https://doi.org/10.7554/eLife.06726 | Rights: | Attribution 4.0 International | Abstract: | A key step in the de novo formation of the embryonic vasculature is the migration of endothelial precursors, the angioblasts, to the position of the future vessels. To form the first axial vessels, angioblasts migrate towards the midline and coalesce underneath the notochord. Vascular endothelial growth factor (Vegf) has been proposed to serve as a chemoattractant for the angioblasts and to regulate this medial migration. Here we challenge this model and instead demonstrate that angioblasts rely on their intrinsic expression of Apelin receptors (Aplr, APJ) for their migration to the midline. We further show that during this angioblast migration Apelin receptor signaling is mainly triggered by the recently discovered ligand Elabela (Ela). As neither of the ligands Ela or Apelin (Apln) nor their receptors have previously been implicated in regulating angioblast migration, we hereby provide a novel mechanism for regulating vasculogenesis, with direct relevance to physiological and pathological angiogenesis. © 2015, eLife Sciences Publications Ltd. All rights reserved. | Source Title: | eLife | URI: | https://scholarbank.nus.edu.sg/handle/10635/180337 | ISSN: | 2050084X | DOI: | 10.7554/eLife.06726 | Rights: | Attribution 4.0 International |
Appears in Collections: | Elements Staff Publications |
Show full item record
Files in This Item:
File | Description | Size | Format | Access Settings | Version | |
---|---|---|---|---|---|---|
10_7554_eLife_06726.pdf | 4.68 MB | Adobe PDF | OPEN | None | View/Download |
This item is licensed under a Creative Commons License