High-Level Erythroid Lineage-Directed Gene Expression Using Globin Gene Regulatory Elements After Lentiviral Vector-Mediated Gene Transfer into Primitive Human and Murine Hematopoietic Cells
- 20 November 2002
- journal article
- research article
- Published by Mary Ann Liebert Inc in Human Gene Therapy
- Vol. 13 (17) , 2007-2016
- https://doi.org/10.1089/10430340260395866
Abstract
Lentiviral vectors efficiently transduce primitive human hematopoietic cells and are capable of transferring complex genomes. Vectors were designed with hypersensitive sites containing regulatory elements from the β-globin locus control region linked to the β-globin gene promoter to drive expression of the enhanced green fluorescent protein marker to facilitate analysis of the pattern of gene expression in various hematopoietic lineages. Such vectors gave higher level, induced expression in mouse erythroleukemia cells than a previously described vector that utilized an enhancer from the α locus and the ankyrin-1 promoter [Moreau-Gaudry, F., Xia, P., Jiang, G., Perelman, N.P., Bauer, G., Ellis, J., Surinya, K.H., Mavilio, F., Shen, C.K., and Malik, P. (2001). Blood 98, 2664-2672]. The addition of γ-globin intron sequences further augmented vector expression. Expression was also effectively targeted to the erythroid lineage in cultured human cells from peripheral blood and in mouse red blood cells in vivo, although lower levels of expression were also observed in other lineages. Thus, these newly described vectors provide a means to achieve high-level gene expression, predominantly in erythroid cells, an outcome that may have potential therapeutic application.Keywords
This publication has 37 references indexed in Scilit:
- The zinc-finger proto-oncogene Gfi-1b is essential for development of the erythroid and megakaryocytic lineagesGenes & Development, 2002
- Correction of Sickle Cell Disease in Transgenic Mouse Models by Gene TherapyScience, 2001
- Long-Term Engraftment of Nonobese Diabetic/Severe Combined Immunodeficient Mice with Human CD34+Cells Transduced by a Self-Inactivating Human Immunodeficiency Virus Type 1 VectorHuman Gene Therapy, 2001
- Lentivirus Vector-Mediated Hematopoietic Stem Cell Gene Transfer of Common Gamma-Chain Cytokine Receptor in Rhesus MacaquesJournal of Virology, 2001
- Efficient Human Immunodeficiency Virus-Based Vector Transduction of Unstimulated Human Mobilized Peripheral Blood CD34+Cells in the SCID-hu Thy/Liv Model of Human T Cell LymphopoiesisHuman Gene Therapy, 2001
- Critical Factors Influencing Stable Transduction of Human CD34+ Cells with HIV-1-Derived Lentiviral VectorsMolecular Therapy, 2000
- Transduction of Human CD34+CD38- Bone Marrow and Cord Blood-Derived SCID-Repopulating Cells with Third-Generation Lentiviral VectorsMolecular Therapy, 2000
- Gene Therapy of Human Severe Combined Immunodeficiency (SCID)-X1 DiseaseScience, 2000
- Marking and Gene Expression by a Lentivirus Vector in Transplanted Human and Nonhuman Primate CD34+CellsJournal of Virology, 2000
- Multilineage gene expression precedes commitment in the hemopoietic system.Genes & Development, 1997