Retrovirus receptor mRNA expression correlates with gene transfer efficiency in pluripotent hematopoietic stem cells

Leukemia. 1999 Apr:13 Suppl 1:S52-4. doi: 10.1038/sj.leu.2401287.

Abstract

Hematopoietic stem cells (HSC) from bone marrow, peripheral blood and cord blood are important in clinical transplantation. However, their use in gene therapy protocols is still limited by a low level of transduction efficiency. In addition to the cell cycling block to retrovirus transduction, we recently demonstrated that the low level of retrovirus receptor mRNA in mouse HSC correlated with the low level of amphotropic retrovirus transduction in these cells. Similarly, we found low levels of mRNA encoding the amphotropic retrovirus receptor in human bone marrow Lin CD34+ CD38- HSC. In an effort to identify an alternative population of human HSC that might be more efficiently transduced, we assayed HSC populations from cord blood for mRNA encoding the amphotropic retrovirus receptor. High levels of receptor mRNA were present in HSC from previously cryopreserved cord blood compared with HSC from fresh bone marrow and fresh cord blood. The HSC from cryopreserved cord blood are excellent candidates for gene therapy protocols.

MeSH terms

  • Adult
  • Animals
  • Antigens, CD34 / analysis
  • Blood Preservation
  • Bone Marrow Cells / drug effects
  • Bone Marrow Cells / metabolism
  • Bone Marrow Cells / virology
  • Cell Lineage
  • Cryopreservation
  • Fetal Blood / cytology
  • Granulocyte Colony-Stimulating Factor / pharmacology
  • Hematopoietic Stem Cell Mobilization
  • Hematopoietic Stem Cells / metabolism*
  • Hematopoietic Stem Cells / virology
  • Humans
  • Infant, Newborn
  • Membrane Glycoproteins / biosynthesis
  • Membrane Glycoproteins / genetics
  • Membrane Glycoproteins / physiology*
  • Mice
  • Mice, Inbred C57BL
  • Phosphate Transport Proteins*
  • RNA, Messenger / biosynthesis*
  • RNA, Messenger / genetics
  • Receptors, Virus / biosynthesis
  • Receptors, Virus / genetics
  • Receptors, Virus / physiology*
  • Sodium-Phosphate Cotransporter Proteins
  • Stem Cell Factor / pharmacology
  • Symporters*
  • Tissue Preservation
  • Transfection*

Substances

  • Antigens, CD34
  • Membrane Glycoproteins
  • Phosphate Transport Proteins
  • RNA, Messenger
  • Receptors, Virus
  • Sodium-Phosphate Cotransporter Proteins
  • Stem Cell Factor
  • Symporters
  • ecotropic murine leukemia virus receptor
  • Granulocyte Colony-Stimulating Factor