PUBLICATION

TRPC1 Is Essential for In Vivo Angiogenesis in Zebrafish

Authors
Yu, P.C., Gu, S.Y., Bu, J.W., and Du, J.L.
ID
ZDB-PUB-100302-15
Date
2010
Source
Circulation research   106(7): 1221-1232 (Journal)
Registered Authors
Du, Jiu Lin
Keywords
TRPC1, VEGF, ISV, angiogenesis, zebrafish
MeSH Terms
  • Animals
  • Animals, Genetically Modified
  • Blood Vessels/embryology
  • Blood Vessels/metabolism*
  • Cell Movement
  • Cell Proliferation
  • Endothelial Cells/metabolism*
  • Endothelial Cells/transplantation
  • Enzyme Activation
  • Extracellular Signal-Regulated MAP Kinases/metabolism
  • Gene Expression Regulation, Developmental
  • Gene Knockdown Techniques
  • Microscopy, Confocal
  • Microscopy, Video
  • Neovascularization, Physiologic*
  • Oligonucleotides, Antisense/metabolism
  • Phosphorylation
  • Pseudopodia/metabolism
  • RNA, Messenger/metabolism
  • Signal Transduction
  • TRPC Cation Channels/genetics
  • TRPC Cation Channels/metabolism*
  • Vascular Endothelial Growth Factor A/metabolism
  • Zebrafish/embryology
  • Zebrafish/genetics
  • Zebrafish/metabolism*
(all 26)
PubMed
20185799 Full text @ Circ. Res.
Abstract
Rationale: Wiring vascular and neural networks are known to share common molecular signaling pathways. Activation of transient receptor potential type C channels (TRPCs) has recently been shown to underlie chemotropic guidance of neural axons. It is thus of interest to examine whether TRPCs are also involved in vascular development. Objective: To determine the role of TRPC1 in angiogenesis in vivo during zebrafish development. Methods and Results: Knockdown of zebrafish trpc1 by antisense morpholino oligonucleotides severely disrupted angiogenic sprouting of intersegmental vessels (ISVs) in zebrafish larvae. This angiogenic defect was prevented by overexpression of a morpholino oligonucleotide-resistant form of zebrafish trpc1 mRNA. Cell transplantation analysis showed that this requirement of Trpc1 for ISV growth was endothelial cell-autonomous. In vivo, time-lapse imaging further revealed that the angiogenic defect was attributable to impairment of filopodia extension, migration, and proliferation of ISV tip cells. Furthermore, Trpc1 acted synergistically with vascular endothelial growth factor A (Vegf-a) in controlling ISV growth, and appeared to be downstream to Vegf-a in controlling angiogenesis, as evidence by the findings that Trpc1 was required for Vegf-a-induced ectopic angiogenesis of subintestinal veins and phosphorylation of extracellular signal-regulated kinase. Conclusions: These results provide the first in vivo evidence that TRPC1 is essential for angiogenesis, reminiscent of the role of TRPCs in axon guidance. It implicates that TRPC1 may represent a potential target for treating pathological angiogenesis.
Genes / Markers
Marker Marker Type Name
efnb2aGENEephrin-B2a
ephb4aGENEeph receptor B4a
flt4GENEfms related receptor tyrosine kinase 4
notch3GENEnotch receptor 3
tbx20GENET-box transcription factor 20
trpc1GENEtransient receptor potential cation channel, subfamily C, member 1
vegfaaGENEvascular endothelial growth factor Aa
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Expression
Phenotype
Mutations / Transgenics
Allele Construct Type Affected Genomic Region
y1TgTransgenic Insertion
    y7TgTransgenic Insertion
      1 - 2 of 2
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      Human Disease / Model
      No data available
      Sequence Targeting Reagents
      Target Reagent Reagent Type
      trpc1MO1-trpc1MRPHLNO
      trpc1MO2-trpc1MRPHLNO
      vegfaaMO1-vegfaaMRPHLNO
      1 - 3 of 3
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      Fish
      Antibodies
      Name Type Antigen Genes Isotypes Host Organism
      Ab9-mapkmonoclonal
        IgGRabbit
        1 - 1 of 1
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        Orthology
        Engineered Foreign Genes
        Marker Marker Type Name
        EGFPEFGEGFP
        1 - 1 of 1
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        Mapping