Analysis of histone 2B-GFP retention reveals slowly cycling hematopoietic stem cells

Nat Biotechnol. 2009 Jan;27(1):84-90. doi: 10.1038/nbt.1517. Epub 2008 Dec 5.


Hematopoietic stem cells (HSCs) are thought to divide infrequently based on their resistance to cytotoxic injury targeted at rapidly cycling cells and have been presumed to retain labels such as the thymidine analog 5-bromodeoxyuridine (BrdU). However, BrdU retention is neither a sensitive nor specific marker for HSCs. Here we show that transient, transgenic expression of a histone 2B (H2B)-green fluorescent protein (GFP) fusion protein in mice has several advantages for label-retention studies over BrdU, including rapid induction of H2B-GFP in virtually all HSCs, higher labeling intensity and the ability to prospectively study label-retaining cells, which together permit a more precise analysis of division history. Mathematical modeling of H2B-GFP dilution in HSCs, identified with a stringent marker combination (L(-)K(+)S(+)CD48(-)CD150(+)), revealed unexpected heterogeneity in their proliferation rates and showed that approximately 20% of HSCs divide at an extremely low rate (< or =0.8-1.8% per day).

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antigens, CD / biosynthesis
  • Bone Marrow Cells / cytology
  • Bromodeoxyuridine / pharmacology
  • CD48 Antigen
  • Cell Differentiation
  • Cell Lineage
  • Flow Cytometry / methods
  • Green Fluorescent Proteins / metabolism*
  • Hematopoietic Stem Cell Transplantation / methods
  • Hematopoietic Stem Cells / cytology
  • Histones / chemistry*
  • Humans
  • Mice
  • Models, Theoretical
  • Receptors, Cell Surface / biosynthesis
  • Signaling Lymphocytic Activation Molecule Family Member 1


  • Antigens, CD
  • CD48 Antigen
  • CD48 protein, human
  • Cd48 protein, mouse
  • Histones
  • Receptors, Cell Surface
  • SLAMF1 protein, human
  • Green Fluorescent Proteins
  • Signaling Lymphocytic Activation Molecule Family Member 1
  • Bromodeoxyuridine