Gene expression profiling related to the enhanced erythropoiesis in mouse bone marrow cells

J Cell Biochem. 2008 May 1;104(1):295-303. doi: 10.1002/jcb.21620.

Abstract

Peroxiredoxin II knockout (Prdx II(-/-)) mice had a spontaneous phenotype of hemolytic anemia. In this study, we found that Ter-119(+)CD71(+) cells increased in Prdx II(-/-) mice bone marrow (BM) at 8 weeks of age. We examined the differential expression profiles to bone marrow cells (BMCs) between Prdx II(+/+) and Prdx II(-/-) mice using a cDNA microarray. We identified the 136 candidates were differentially expressed a greater twofold increase or decrease than EPO receptor. In this study, we focused on the up-regulated NBPs during erythropoietic differentiation. According to cDNA microarray results, six NBPs except zfp-127 were up-regulated during erythropoiesis in Prdx II(-/-) mice. Among the six candidates, eIF3-p44, hnRNPH1, G3bp, and Zfpm-1 were dramatically increased at day 7 of the in vitro erythropoietic differentiation of human CD34(+) cells. However, DJ-1 and Rbm3 were slightly increased only at day 12. Our results suggest that up-regulated NBPs might be involved during erythropoietic differentiation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anemia, Hemolytic / genetics
  • Animals
  • Antigens, CD34
  • Bone Marrow Cells / physiology
  • Erythropoiesis / genetics*
  • Gene Expression Profiling*
  • Hematopoietic Stem Cells*
  • Humans
  • Mice
  • Mice, Knockout
  • Oligonucleotide Array Sequence Analysis
  • Peroxiredoxins / genetics
  • Receptors, Erythropoietin
  • Up-Regulation

Substances

  • Antigens, CD34
  • Receptors, Erythropoietin
  • PRDX2 protein, human
  • Peroxiredoxins