PUBLICATION

Distinct Cellular Mechanisms of Blood Vessel Fusion in the Zebrafish Embryo

Authors
Herwig, L., Blum, Y., Krudewig, A., Ellertsdottir, E., Lenard, A., and Belting, H.G., and Affolter, M.
ID
ZDB-PUB-111122-9
Date
2011
Source
Current biology : CB   21(22): 1942-1948 (Journal)
Registered Authors
Affolter, Markus, Belting, Heinz-Georg Paul (Henry), Ellertsdottir, Elin
Keywords
none
MeSH Terms
  • Animals, Genetically Modified/anatomy & histology
  • Animals, Genetically Modified/embryology
  • Animals, Genetically Modified/genetics
  • Green Fluorescent Proteins/chemistry
  • Green Fluorescent Proteins/metabolism
  • Membrane Glycoproteins/metabolism
  • Sialoglycoproteins/metabolism
  • Phosphoproteins/metabolism
  • Morphogenesis
  • Cell Membrane/metabolism
  • Animals
  • Membrane Proteins/metabolism
  • Embryo, Nonmammalian/anatomy & histology
  • Embryo, Nonmammalian/embryology
  • Intercellular Junctions/genetics
  • Intercellular Junctions/ultrastructure
  • Zonula Occludens-1 Protein
  • Zebrafish/anatomy & histology
  • Zebrafish/embryology*
  • Zebrafish/genetics
  • Blood Vessels/anatomy & histology
  • Blood Vessels/embryology*
(all 22)
PubMed
22079115 Full text @ Curr. Biol.
Abstract

Although many of the cellular and molecular mechanisms of angiogenesis have been intensely studied [1], little is known about the processes that underlie vascular anastomosis. We have generated transgenic fish lines expressing an EGFP-tagged version of the junctional protein zona occludens 1 (ZO1) to visualize individual cell behaviors that occur during vessel fusion and lumen formation in vivo. These life observations show that endothelial cells (ECs) use two distinct morphogenetic mechanisms, cell membrane invagination and cord hollowing to generate different types of vascular tubes. During initial steps of anastomosis, cell junctions that have formed at the initial site of cell contacts expand into rings, generating a cellular interface of apical membrane compartments, as defined by the localization of the apical marker podocalyxin-2 (Pdxl2). During the cord hollowing process, these apical membrane compartments are brought together via cell rearrangements and extensive junctional remodeling, resulting in lumen coalescence and formation of a multicellular tube. Vessel fusion by membrane invagination occurs adjacent to a preexisting lumen in a proximal to distal direction and is blood-flow dependent. Here, the invaginating inner cell membrane undergoes concomitant apicobasal polarization and the vascular lumen is formed by the extension of a transcellular lumen through the EC, which forms a unicellular or seamless tube.

Genes / Markers
Figures
Figure Gallery (6 images)
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Expression
Phenotype
Mutations / Transgenics
Allele Construct Type Affected Genomic Region
nkuasrfp1aTgTransgenic Insertion
    rk8TgTransgenic Insertion
      s843TgTransgenic Insertion
        ubs3TgTransgenic Insertion
          ubs4TgTransgenic Insertion
            ubs5TgTransgenic Insertion
              ubs6TgTransgenic Insertion
                ubs7TgTransgenic Insertion
                  y1TgTransgenic Insertion
                    1 - 9 of 9
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                    Human Disease / Model
                    No data available
                    Sequence Targeting Reagents
                    Target Reagent Reagent Type
                    tnnt2aMO1-tnnt2aMRPHLNO
                    1 - 1 of 1
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                    Fish
                    Antibodies
                    Name Type Antigen Genes Isotypes Host Organism
                    Ab1-cdh5Rabbit
                    Ab1-podxl2polyclonalRabbit
                    1 - 2 of 2
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                    Orthology
                    No data available
                    Engineered Foreign Genes
                    Marker Marker Type Name
                    EGFPEFGEGFP
                    GAL4FFEFGGAL4FF
                    KaedeEFGKaede
                    RFPEFGRFP
                    1 - 4 of 4
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                    Mapping
                    No data available