Exp Mol Med.  2013 Nov;45(11):e56.

Very small embryonic-like stem-cell optimization of isolation protocols: an update of molecular signatures and a review of current in vivo applications

Affiliations
  • 1Department of Biomedical Sciences, University of Ulsan College of Medicine, Seoul, Korea.
  • 2Stem Cell Institute at James Graham Brown Cancer Center, University of Louisville, Louisville, KY, USA. mzrata01@louisville.edu

Abstract

As the theory of stem cell plasticity was first proposed, we have explored an alternative hypothesis for this phenomenon: namely that adult bone marrow (BM) and umbilical cord blood (UCB) contain more developmentally primitive cells than hematopoietic stem cells (HSCs). In support of this notion, using multiparameter sorting we were able to isolate small Sca1+Lin-CD45- cells and CD133+Lin-CD45- cells from murine BM and human UCB, respectively, which were further enriched for the detection of various early developmental markers such as the SSEA antigen on the surface and the Oct4 and Nanog transcription factors in the nucleus. Similar populations of cells have been found in various organs by our team and others, including the heart, brain and gonads. Owing to their primitive cellular features, such as the high nuclear/cytoplasm ratio and the presence of euchromatin, they are called very small embryonic-like stem cells (VSELs). In the appropriate in vivo models, VSELs differentiate into long-term repopulating HSCs, mesenchymal stem cells (MSCs), lung epithelial cells, cardiomyocytes and gametes. In this review, we discuss the most recent data from our laboratory and other groups regarding the optimal isolation procedures and describe the updated molecular characteristics of VSELs.

Keyword

VSEL; Igf2-H19 locus; Oct4; Sall4

MeSH Terms

Animals
Cell Lineage
Cell Separation/*methods
Embryonic Stem Cells/*cytology/metabolism
Hematopoietic Stem Cells/*cytology/metabolism
Humans
Mesenchymal Stromal Cells/*cytology/metabolism
Pluripotent Stem Cells/cytology/metabolism
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