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Dilivery of Genes to Hematopoietic Stem Cells

  • Masafumi Onodera
Part of the Methods in Molecular Biology™ book series (MIMB, volume 246)

Abstract

Bone marrow hematopoiesis is maintained by hematopoietic stem cells (HSC) (1). Because of their unique features to self-renew and differentiate along all lineages of hematopoietic cells, even a single HSC can completely reconstitute bone marrow hematopoiesis of irradiated recipients (2). Therefore, HSCs are considered to be the ideal target cell population in gene-therapy fields for genetic disorders that are susceptible to bone marrow transplantation (3). However, because most HSCs are quiescent, it is difficult to transduce them using retroviral vectors (4). Furthermore, retroviral vectors, especially Moloney murine leukemia virus (MMLV)-based retroviral vectors that have been commonly used in gene-therapy clinical trials, are very susceptible to de novo methylation in immature cells such as embryonic stem (ES) cells, embryonal carcinoma cells (EC), and HSCs, resulting in shut off/silencing of the transgene expression in vivo (5). This is another obstacle for successful gene delivery into HSCs.

Keywords

Packaging Cell Line Lineage Negative Cell Total Bone Marrow Staining Medium Stem Cell Gene Therapy 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

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Copyright information

© Humana Press Inc., Totowa, NJ 2004

Authors and Affiliations

  • Masafumi Onodera
    • 1
  1. 1.Department of Hematology, Institute of Clinical MedicineUniversity of TsukubaTsukuba, IbarakiJapan

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