Medical Journals

Gene Expression Analysis of Hematopoietic Progenitor Cells Identifies Dlg7 As a Potential Stem Cell Gene.

Authors:
  • Gudmundsson Kristbjorn Orri
  • Thorsteinsson Leifur
  • Sigurjonsson Olafur E
  • Keller Jonathan R
  • Olafsson Karl
  • Egeland Torstein
  • Gudmundsson Sveinn
  • Rafnar Thorunn

From: Cancer and Developmental Biology Laboratory, Center for Cancer Research, National Cancer Institute-Frederick, Maryland, USA. orri@ncifcrf.gov

Stem cells (Dayton, Ohio)

  • Publish Date: Jun 2007
  • ISSN: 1066-5099
  • Volume: 25
  • Issue: 6
  • Pages: 1498-506
  • Medium: Print
  • Language: English
  • Citation (JAMA): Gudmundsson Kristbjorn Orri, Thorsteinsson Leifur, Sigurjonsson Olafur E, et al. Gene Expression Analysis of Hematopoietic Progenitor Cells Identifies Dlg7 As a Potential Stem Cell Gene.. Stem Cells Jun 2007;25:1498-506

Abstract

Inducible hematopoietic stem/progenitor cell lines represent a model for studying genes involved in self-renewal and differentiation. Here, gene expression was studied in the inducible human CD34+ acute myelogenous leukemia cell line KG1 using oligonucleotide arrays and suppression subtractive cloning. Using this approach, we identified Dlg7, the homolog of the Drosophila Dlg1 tumor suppressor gene, as downregulated at the early stages of KG1 differentiation. Similarly, Dlg7 was expressed in normal purified umbilical cord blood CD34+CD38- progenitors but not in the more committed CD34+CD38+ population. Dlg7 expression was not detected in differentiated cells obtained from hematopoietic colonies, nor was expression detected in purified T-cells, B-cells, and monocytes. When analyzed in different types of stem cells, Dlg7 expression was detected in purified human bone marrow-derived CD133+ progenitor cells, human mesenchymal stem cells, and mouse embryonic stem (ES) cells. Overexpression of Dlg7 in mouse ES cells increased their growth rate and reduced the number of EBs emerging upon differentiation. In addition, the EBs were significantly smaller, indicating an inhibition in differentiation. This inhibition was further supported by higher expression of Bmp4, Oct4, Rex1, and Nanog in EBs overexpressing Dlg7 and lower expression of Brachyury. Finally, the Dlg7 protein was detected in liver and colon carcinoma tumors but not in normal adjacent tissues, suggesting a role for the gene in carcinogenesis. In conclusion, our results suggest that Dlg7 has a role in stem cell survival, in maintaining stem cell properties, and in carcinogenesis. Disclosure of potential conflicts of interest is found at the end of this article.

Mesh Headings (Keywords): Antigens, CD34, Antigens, CD38, Blood Cells, Cell Differentiation, Cell Survival, Cells, Cultured, Dendritic Cells, Gene Expression Profiling, Gene Expression Regulation, Hematopoietic Stem Cells, Humans, Neoplasm Proteins, Oligonucleotide Array Sequence Analysis, Transfection, Umbilical Cord


Check for Full Text / PubMed Unique Identifier (PMID): 17322106


This abstract is part of PubMed, a service of the U.S. National Library of Medicine. PubMed includes more than 17 million citations from MEDLINE and other life science journals for biomedical articles. See Copyright and Disclaimers.

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The data herein was last updated on July 8th, 2008 and may not reflect the most current and accurate data available from NLM.


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