Published July 9, 2010 | Version v1
Journal article

Gene expression profiles of cryopreserved CD34+ human umbilical cord blood cells are related to their bone marrow reconstitution abilities in mouse xenografts

  • 1. Cell Engineering Division, RIKEN BioResource Center, Tsukuba (Japan)
  • 2. Department of Cell Biology, The JFCR-Cancer Institute (Japan)
  • 3. Omics Science Center, RIKEN, Yokohama (Japan)

Description

Human umbilical cord blood (UCB) cells are an alternative source of hematopoietic stem cells for treatment of leukemia and other diseases. It is very difficult to assess the quality of UCB cells in the clinical situation. Here, we sought to assess the quality of UCB cells by transplantation to immunodeficient mice. Cryopreserved CD34+ UCB cells from twelve different human donors were transplanted into sublethally irradiated NOD/shi-scid Jic mice. In parallel, the gene expression profiles of the UCB cells were determined from oligonucleotide microarrays. UCB cells from three donors failed to establish an engraftment in the host mice, while the other nine succeeded to various extents. Gene expression profiling indicated that 71 genes, including HOXB4, C/EBP-β, and ETS2, were specifically overexpressed and 23 genes were suppressed more than 2-fold in the successful UCB cells compared to those that failed. Functional annotation revealed that cell growth and cell cycle regulators were more abundant in the successful UCB cells. Our results suggest that hematopoietic ability may vary among cryopreserved UCB cells and that this ability can be distinguished by profiling expression of certain sets of genes.

Availability note (English)

Available from http://dx.doi.org/10.1016/j.bbrc.2010.06.010

Additional details

Identifiers

DOI
10.1016/j.bbrc.2010.06.010;
PII
S0006-291X(10)01113-7;

Publishing Information

Journal Title
Biochemical and Biophysical Research Communications
Journal Volume
397
Journal Issue
4
Journal Page Range
p. 697-705
ISSN
0006-291X
CODEN
BBRCA9

Optional Information

Copyright
Copyright (c) 2010 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.