PUBLICATION

Hemogenic endothelium specification and hematopoietic stem cell maintenance employ distinct Scl isoforms

Authors
Zhen, F., Lan, Y., Yan, B., Zhang, W., and Wen, Z.
ID
ZDB-PUB-130927-27
Date
2013
Source
Development (Cambridge, England)   140(19): 3977-3985 (Journal)
Registered Authors
Wen, Zilong
Keywords
zebrafish, Scl, Tal1, hemogenic endothelium, hematopoietic stem cells
MeSH Terms
  • Zebrafish Proteins/genetics
  • Zebrafish Proteins/metabolism*
  • Animals
  • Male
  • Proto-Oncogene Proteins/genetics
  • Proto-Oncogene Proteins/metabolism*
  • Zebrafish
  • Hemangioblasts/cytology*
  • Hemangioblasts/metabolism*
  • Female
  • Basic Helix-Loop-Helix Transcription Factors/genetics
  • Basic Helix-Loop-Helix Transcription Factors/metabolism*
  • In Situ Hybridization
  • Microscopy, Confocal
  • Hematopoietic Stem Cells/cytology*
  • Hematopoietic Stem Cells/metabolism*
  • Protein Isoforms/genetics
  • Protein Isoforms/metabolism*
  • Cells, Cultured
(all 19)
PubMed
24046317 Full text @ Development
Abstract

Recent studies have shown that nascent hematopoietic stem cells (HSCs) derive directly from the ventral aortic endothelium (VAE) via endothelial to hematopoietic transition (EHT). However, whether EHT initiates from a random or predetermined subpopulation of VAE, as well as the molecular mechanism underlying this process, remain unclear. We previously reported that different zebrafish stem cell leukemia (scl) isoforms are differentially required for HSC formation in the ventral wall of the dorsal aorta. However, the exact stage at which these isoforms impact HSC development was not defined. Here, using in vivo time-lapse imaging of scl isoform-specific reporter transgenic zebrafish lines, we show that prior to EHT scl-β is selectively expressed in hemogenic endothelial cells, a unique subset of VAE cells possessing hemogenic potential, whereas scl-α is expressed later in nascent HSCs as they egress from VAE cells. In accordance with their expression, loss-of-function studies coupled with in vivo imaging analysis reveal that scl-β acts earlier to specify hemogenic endothelium, which is later transformed by runx1 into HSCs. Our results also reveal a previously unexpected role of scl-α in maintaining newly born HSCs in the aorta-gonads-mesonephros. Thus, our data suggest that a defined hemogenic endothelial population preset by scl-β supports the deterministic emergence of HSCs, and unravel the cellular mechanisms by which scl isoforms regulate HSC development.

Genes / Markers
Figures
Figure Gallery (13 images) / 2
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Expression
Phenotype
Mutations / Transgenics
Allele Construct Type Affected Genomic Region
hg1
    Point Mutation
    hkz06tTgTransgenic Insertion
      hkz07tTgTransgenic Insertion
        hkz08tTgTransgenic Insertion
          la2TgTransgenic Insertion
            s843TgTransgenic Insertion
              s896TgTransgenic Insertion
                zf169TgTransgenic Insertion
                  1 - 8 of 8
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                  Human Disease / Model
                  No data available
                  Sequence Targeting Reagents
                  Target Reagent Reagent Type
                  runx1MO2-runx1MRPHLNO
                  runx1MO3-runx1MRPHLNO
                  tal1MO7-tal1MRPHLNO
                  tal1MO8-tal1MRPHLNO
                  1 - 4 of 4
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                  Fish
                  Antibodies
                  No data available
                  Orthology
                  No data available
                  Engineered Foreign Genes
                  Marker Marker Type Name
                  d2EGFPEFGd2EGFP
                  DsRedEFGDsRed
                  EGFPEFGEGFP
                  mCherryEFGmCherry
                  1 - 4 of 4
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                  Mapping
                  No data available