Transcription profiling of adult and fetal human neuroprogenitors identifies divergent paths to maintain the neuroprogenitor cell state

Research output: Contribution to journalResearch articleContributedpeer-review

Contributors

  • Martina Maisel - , Department of Neurology (Author)
  • Alexander Herr - , Hereditary Cancer Syndrome Center (Author)
  • Javorina Milosevic - , Leipzig University (Author)
  • Andreas Hermann - , Department of Neurology (Author)
  • Hans Jörg Habisch - , Ulm University (Author)
  • Sigrid Schwarz - , Leipzig University (Author)
  • Matthias Kirsch - , Department of Neurosurgery (Author)
  • Gregor Antoniadis - , Ulm University (Author)
  • Rolf Brenner - , Ulm University (Author)
  • Susanne Hallmeyer-Elgner - , Department of Neurology (Author)
  • Holger Lerche - , Ulm University (Author)
  • Johannes Schwarz - , Leipzig University (Author)
  • Alexander Storch - , Department of Neurology (Author)

Abstract

Global gene expression profiling was performed using RNA from adult human hippocampus-derived neuroprogenitor cells (NPCs) and multipotent frontal cortical fetal NPCs compared with adult human mesenchymal stem cells (hMSCs) as a multipotent adult stem cell control, and adult human hippocampal tissue, to define a gene expression pattern that is specific for human NPCs. The results were compared with data from various databases. Hierarchical cluster analysis of all neuroectodermal cell/tissue types revealed a strong relationship of adult hippocampal NPCs with various white matter tissues, whereas fetal NPCs strongly correlate with fetal brain tissue. However, adult and fetal NPCs share the expression of a variety of genes known to be related to signal transduction, cell metabolism and neuroectodermal tissue. In contrast, adult NPCs and hMSCs overlap in the expression of genes mainly involved in extracellular matrix biology. We present for the first time a detailed transcriptome analysis of human adult NPCs suggesting a relationship between hippocampal NPCs and white matter-derived precursor cells. We further provide a framework for standardized comparative gene expression analysis of human brain-derived NPCs with other stem cell populations or differentiated tissues.

Details

Original languageEnglish
Pages (from-to)1231-1240
Number of pages10
JournalStem cells
Volume25
Issue number5
Publication statusPublished - May 2007
Peer-reviewedYes

External IDs

PubMed 17218394

Keywords

Keywords

  • Gene chips, Gene expression profile, Mesenchymal stem cells, Neural stem cells, Neuroprogenitors