Sox17 Dependence Distinguishes the Transcriptional Regulation of Fetal from Adult Hematopoietic Stem Cells

Injune Kim, Thomas L. Saunders, Sean J. Morrison

Research output: Contribution to journalArticle

274 Citations (Scopus)

Abstract

Fetal stem cells differ phenotypically and functionally from adult stem cells in diverse tissues. However, little is known about how these differences are regulated. To address this we compared the gene expression profiles of fetal versus adult hematopoietic stem cells (HSCs) and discovered that the Sox17 transcriptional regulator is specifically expressed in fetal and neonatal but not adult HSCs. Germline deletion of Sox17 led to severe fetal hematopoietic defects, including a lack of detectable definitive HSCs. Conditional deletion of Sox17 from hematopoietic cells led to the loss of fetal and neonatal but not adult HSCs. HSCs stopped expressing Sox17 approximately 4 weeks after birth. During this transition, loss of Sox17 expression correlated with slower proliferation and the acquisition of an adult phenotype by individual HSCs. Sox17 is thus required for the maintenance of fetal and neonatal HSCs and distinguishes their transcriptional regulation from adult HSCs.

Original languageEnglish (US)
Pages (from-to)470-483
Number of pages14
JournalCell
Volume130
Issue number3
DOIs
StatePublished - Aug 10 2007

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Adult Stem Cells
Hematopoietic Stem Cells
Stem cells
Fetal Stem Cells
Transcriptome
Gene expression
Maintenance
Parturition
Phenotype
Tissue
Defects

Keywords

  • DEVBIO
  • STEMCELL

ASJC Scopus subject areas

  • Cell Biology
  • Molecular Biology

Cite this

Sox17 Dependence Distinguishes the Transcriptional Regulation of Fetal from Adult Hematopoietic Stem Cells. / Kim, Injune; Saunders, Thomas L.; Morrison, Sean J.

In: Cell, Vol. 130, No. 3, 10.08.2007, p. 470-483.

Research output: Contribution to journalArticle

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