Abstract

The difficulties associated with studying molecular mechanisms important in hemopoietic stem cell (HSC) function such as the problems of purifying homogeneous stem cell populations, have prompted us to adapt the murine ES cell system as an in vitro model of HSC generation and function. We now report that careful analysis of the time course of HSC generation in differentiating ES cells allows them to be used as a source of known and novel hemopoietic gene products. We have generated a subtracted library using cDNA from ES cells collected just prior to and just following the emergence of HSCs. Analysis of this library shows it to be a rich source of known hemopoietic and hemopoietic related gene products with 44% of identifiable cDNAs falling into these camps. We have demonstrated the value of this system as a source of novel genes of relevance to HSC function by characterizing a novel membrane protein encoding cDNA that is preferentially expressed in primitive hemopoietic cells. Intriguingly, further analysis of the known components of the subtracted library is suggestive of erythroid preconditioning of the ES cell-derived HSC. We have used dot-blot and in situ analysis to indicate that this erythroid preconditioning is probably restricted to primitive but not definitive HSC.

Highlights

  • ¶ Present address: Academic Unit of Obstetrics, Gynaecology and Reproductive Healthcare, St

  • We report that careful analysis of the time course of hemopoietic stem cell (HSC) generation in differentiating embryonal stem (ES) cells allows them to be used as a source of known and novel hemopoietic gene products

  • Despite the absence of detectable mature hemopoietic cells in the embryoid bodies (EBs), a large number of the hemopoietic gene products differentially expressed in concert with the emergence of stem cells in the EBs are more typically associated with mature elements of the erythroid lineage

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Summary

Introduction

¶ Present address: Academic Unit of Obstetrics, Gynaecology and Reproductive Healthcare, St. We have demonstrated the value of this system as a source of novel genes of relevance to HSC function by characterizing a novel membrane protein encoding cDNA that is preferentially expressed in primitive hemopoietic cells.

Results
Conclusion
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