Differential gene expression profiling of CD34+ CD133+ umbilical cord blood hematopoietic stem progenitor cells

被引:52
作者
He, XH
Gonzalez, V
Tsang, A
Thompson, J
Tsang, TC
Harris, DT
机构
[1] Univ Arizona, Dept Immunol & Microbiol, Gene Therapy Grp, Tucson, AZ 85724 USA
[2] Univ Arizona, Dept Pharmacol & Toxicol, Tucson, AZ 85724 USA
[3] Univ Arizona, Coll Nursing, Tucson, AZ 85724 USA
[4] Univ Calif Berkeley, Dept Mol & Cell Biol, Berkeley, CA 94720 USA
关键词
D O I
10.1089/scd.2005.14.188
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Umbilical cord blood (CB)-derived primitive hematopoietic stem progenitor cells (HSPC) are a promising source for stem cell-based gene therapy due to the reduced incidence and severity of graft-versus-host disease (GVHD) after human leukocyte antigen (HLA)-disparate CB transplantation. Cell-surface markers such as CD34 and CD133 have been used in combination to enrich primitive HSPC for research and clinical applications. To understand the molecular characteristics of the CB HSPC, we compared the global gene expression of freshly isolated CB CD34(+)CD133(+) cells with their progenies using a cDNA microarray containing 22,000 human cDNA clones printed on a single chip. A total of 139 genes were differentially expressed between CB HSPC and their progenies. These transcripts included a number of known genes that might play roles in key functions of CB HSPC as well as many genes of unknown function. Among the genes showing the greatest differential expression levels in HSPC were: psoriasin 1, CRHBP, HDAC3, MLLT3, HBEX2, SPINK2, c-kit, H2BFQ, CD133, HHEX, TCF4, ALDH1A1, and FHL1. These data provide more information on the molecular phenotype of CB HSPC and may lead to the identification of new genes critical to stem cell function.
引用
收藏
页码:188 / 198
页数:11
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