Identification of endoglin as a functional marker that defines long-term repopulating hematopoietic stem cells

Proc Natl Acad Sci U S A. 2002 Nov 26;99(24):15468-73. doi: 10.1073/pnas.202614899. Epub 2002 Nov 15.

Abstract

We describe a strategy to obtain highly enriched long-term repopulating (LTR) hematopoietic stem cells (HSCs) from bone marrow side-population (SP) cells by using a transgenic reporter gene driven by a stem cell enhancer. To analyze the gene-expression profile of the rare HSC population, we developed an amplification protocol termed "constant-ratio PCR," in which sample and control cDNAs are amplified in the same PCR. This protocol allowed us to identify genes differentially expressed in the enriched LTR-HSC population by oligonucleotide microarray analysis using as little as 1 ng of total RNA. Endoglin, an ancillary transforming growth factor beta receptor, was differentially expressed by the enriched HSCs. Importantly, endoglin-positive cells, which account for 20% of total SP cells, contain all the LTR-HSC activity within bone marrow SP. Our results demonstrate that endoglin, which plays important roles in angiogenesis and hematopoiesis, is a functional marker that defines LTR HSCs. Our overall strategy may be applicable for the identification of markers for other tissue-specific stem cells.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Animals, Congenic
  • Antigens, CD
  • Biomarkers
  • Bone Marrow Cells / cytology
  • Cell Lineage
  • Colony-Forming Units Assay
  • DNA, Complementary / genetics
  • Endoglin
  • Female
  • Flow Cytometry
  • Gene Expression Profiling
  • Gene Expression Regulation
  • Hematopoietic Stem Cell Transplantation
  • Hematopoietic Stem Cells / chemistry
  • Hematopoietic Stem Cells / cytology*
  • Mice
  • Mice, Inbred C57BL
  • Mice, Inbred NOD
  • Mice, SCID
  • Mice, Transgenic
  • Oligonucleotide Array Sequence Analysis
  • Polymerase Chain Reaction / methods
  • Radiation Chimera
  • Receptors, Cell Surface
  • Subtraction Technique
  • Vascular Cell Adhesion Molecule-1 / genetics
  • Vascular Cell Adhesion Molecule-1 / physiology*

Substances

  • Antigens, CD
  • Biomarkers
  • DNA, Complementary
  • ENG protein, human
  • Endoglin
  • Receptors, Cell Surface
  • Vascular Cell Adhesion Molecule-1