PUBLICATION

Gcsf-Chr19 Promotes Neutrophil Migration to Damaged Tissue through Blood Vessels in Zebrafish

Authors
Galdames, J.A., Zuñiga-Traslaviña, C., Reyes, A.E., Feijóo, C.G.
ID
ZDB-PUB-140604-5
Date
2014
Source
Journal of immunology (Baltimore, Md. : 1950)   193(1): 372-8 (Journal)
Registered Authors
Feijoo, Carmen G., Galdames, Jorge
Keywords
none
MeSH Terms
  • Gene Knockdown Techniques
  • Zebrafish/genetics
  • Zebrafish/immunology*
  • Cell Movement/genetics
  • Cell Movement/immunology*
  • Time Factors
  • Transcription, Genetic/genetics
  • Transcription, Genetic/immunology
  • Wounds and Injuries/genetics
  • Wounds and Injuries/immunology
  • Wounds and Injuries/pathology
  • Neutrophil Infiltration/genetics
  • Neutrophil Infiltration/immunology*
  • Neutrophils/immunology*
  • Neutrophils/pathology
  • Neovascularization, Physiologic/genetics
  • Neovascularization, Physiologic/immunology
  • Zebrafish Proteins/immunology*
  • Zebrafish Proteins/isolation & purification
  • Signal Transduction/genetics
  • Signal Transduction/immunology
  • Granulocyte Colony-Stimulating Factor/genetics
  • Granulocyte Colony-Stimulating Factor/immunology*
  • Animals
(all 24)
PubMed
24890728 Full text @ J. Immunol.
Abstract
G-CSF is an essential cytokine that regulates proliferation and differentiation of granulocytes from hematopoietic stem and progenitor cells. In mammals G-CSF has been identified as a key factor that promotes the release of neutrophils from the bone marrow into the blood circulation. In silico analysis indicates that zebrafish has two gcsf genes, gcsf-chr12 in chromosome 12 and gcsf-chr19 in chromosome 19. Gcsf-Chr12 participates in emergency myelopoiesis, but, in contrast to its mammalian orthologue, is not involved in neutrophil migration toward damaged tissue. In turn, the function of Gcsf-Chr19 has not been examined yet. In this study, we analyzed the role of Gcsf-Chr19 in regulating neutrophil migration toward the wound. Our results indicated that during the first h after caudal fin transection, neutrophils migrate from the hematopoietic tissue toward the injury, using the extracellular matrix as a substrate. Later, between 3 and 4 h postdamage, the recruitment mainly occurs through the bloodstream, and only a few neutrophils still use the extracellular matrix to migrate. During this process, the transcriptional levels of gcsf-chr19 are considerably increased, reaching a peak 1 h postdamage. The knockdown of Gcsf-chr19 indicated that the percentage of neutrophils that reach the wound decreased after the first h postinjury, suggesting that the knockdown specifically affects neutrophils that travel to the wound through blood vessels. Together, our data provide novel information about the regulation of neutrophil migration in zebrafish, positioning Gcsf-Chr19 as a key signal during the course of an inflammatory process triggered by severe damage.
Genes / Markers
Figures
No images available
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Expression
Phenotype
Mutations / Transgenics
Allele Construct Type Affected Genomic Region
i114TgTransgenic Insertion
    y1TgTransgenic Insertion
      zf106TgTransgenic Insertion
        1 - 3 of 3
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        Human Disease / Model
        No data available
        Sequence Targeting Reagents
        Target Reagent Reagent Type
        csf3bMO1-csf3bMRPHLNO
        csf3bMO2-csf3bMRPHLNO
        1 - 2 of 2
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        Fish
        Antibodies
        Orthology
        Engineered Foreign Genes
        Marker Marker Type Name
        EGFPEFGEGFP
        GFPEFGGFP
        1 - 2 of 2
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        Mapping