PUBLICATION

Complex cell rearrangements during intersegmental vessel sprouting and vessel fusion in the zebrafish embryo

Authors
Blum, Y., Belting, H.G., Ellertsdottir, E., Herwig, L., Lüders, F., and Affolter, M.
ID
ZDB-PUB-080326-18
Date
2008
Source
Developmental Biology   316(2): 312-322 (Journal)
Registered Authors
Affolter, Markus, Belting, Heinz-Georg Paul (Henry), Ellertsdottir, Elin
Keywords
Angiogenesis, ISV, Vessel fusion, VE-cadherin, Adherens junctions, Transgenic, ZO-1, Zebrafish
MeSH Terms
  • Embryo, Nonmammalian/cytology*
  • Embryo, Nonmammalian/physiology*
  • Endothelium, Vascular/cytology
  • Endothelium, Vascular/embryology
  • Endothelium, Vascular/physiology
  • Cell Fusion
  • Animals, Genetically Modified
  • Animals
  • Cell Division
  • Plasmids
  • Zebrafish/embryology*
  • Zebrafish/genetics
(all 12)
PubMed
18342303 Full text @ Dev. Biol.
Abstract
The formation of intersegmental blood vessels (ISVs) in the zebrafish embryo serves as a paradigm to study angiogenesis in vivo. ISV formation is thought to occur in discrete steps. First, endothelial cells of the dorsal aorta migrate out and align along the dorsoventral axis. The dorsal-most cell, also called tip cell, then joins with its anterior and posterior neighbours, thus establishing a simple vascular network. The vascular lumen is then established via formation of vacuoles, which eventually fuse with those of adjacent endothelial cells to generate a seamless tube with an intracellular lumen. To investigate the cellular architecture and the development of ISVs in detail, we have analysed the arrangement of endothelial cell junctions and have performed single cell live imaging. In contrast to previous reports, we find that endothelial cells are not arranged in a linear head-to-tail configuration but overlap extensively and form a multicellular tube, which contains an extracellular lumen. Our studies demonstrate that a number of cellular behaviours, such as cell divisions, cell rearrangements and dynamic alterations in cell-cell contacts, have to be considered when studying the morphological and molecular processes involved in ISV and endothelial lumen formation in vivo.
Genes / Markers
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Phenotype
No data available
Mutations / Transgenics
Allele Construct Type Affected Genomic Region
s843TgTransgenic Insertion
    ubs1TgTransgenic Insertion
      y1TgTransgenic Insertion
        1 - 3 of 3
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        Human Disease / Model
        No data available
        Sequence Targeting Reagents
        No data available
        Fish
        1 - 3 of 3
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        Antibodies
        Name Type Antigen Genes Isotypes Host Organism
        Ab1-cdh5Rabbit
        Ab1-tjp1monoclonalIgG1Mouse
        1 - 2 of 2
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        Orthology
        No data available
        Engineered Foreign Genes
        Marker Marker Type Name
        EGFPEFGEGFP
        1 - 1 of 1
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        Mapping
        No data available