A population of very small embryonic-like (VSEL) CXCR4(+)SSEA-1(+)Oct-4+ stem cells identified in adult bone marrow

Leukemia. 2006 May;20(5):857-69. doi: 10.1038/sj.leu.2404171.

Abstract

By employing multiparameter sorting, we identified in murine bone marrow (BM) a homogenous population of rare (approximately 0.02% of BMMNC) Sca-1(+)lin(-)CD45- cells that express by RQ-PCR and immunohistochemistry markers of pluripotent stem cells (PSC) such as SSEA-1, Oct-4, Nanog and Rex-1. The direct electronmicroscopical analysis revealed that these cells are small (approximately 2-4 microm), posses large nuclei surrounded by a narrow rim of cytoplasm, and contain open-type chromatin (euchromatin) that is typical for embryonic stem cells. In vitro cultures these cells are able to differentiate into all three germ-layer lineages. The number of these cells is highest in BM from young (approximately 1-month-old) mice and decreases with age. It is also significantly diminished in short living DBA/2J mice as compared to long living B6 animals. These cells in vitro respond strongly to SDF-1, HGF/SF and LIF and express CXCR4, c-met and LIF-R, respectively, and since they adhere to fibroblasts they may be coisolated with BM adherent cells. We hypothesize that this population of Sca-1(+)lin(-)CD45- very small embryonic-like (VSEL) stem cells is deposited early during development in BM and could be a source of pluripotent stem cells for tissue/organ regeneration.

Publication types

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

MeSH terms

  • Age Factors
  • Animals
  • Bone Marrow Cells / cytology*
  • Cell Differentiation / physiology
  • Cell Separation
  • Cells, Cultured
  • Embryo, Mammalian / cytology
  • Female
  • In Vitro Techniques
  • Lewis X Antigen / biosynthesis*
  • Lewis X Antigen / genetics
  • Mice
  • Mice, Inbred C57BL
  • Mice, Inbred DBA
  • Myocytes, Cardiac / cytology
  • Myocytes, Cardiac / physiology
  • Neurons / cytology
  • Neurons / physiology
  • Octamer Transcription Factor-3 / biosynthesis*
  • Octamer Transcription Factor-3 / genetics
  • Pancreas / cytology
  • Pancreas / physiology
  • Proto-Oncogene Proteins c-met / genetics
  • Receptors, CXCR4 / biosynthesis*
  • Receptors, CXCR4 / genetics
  • Reverse Transcriptase Polymerase Chain Reaction
  • STAT3 Transcription Factor / genetics
  • Stem Cells / classification
  • Stem Cells / cytology*
  • Stem Cells / metabolism*

Substances

  • Lewis X Antigen
  • Octamer Transcription Factor-3
  • Receptors, CXCR4
  • STAT3 Transcription Factor
  • Proto-Oncogene Proteins c-met