Stromal cells maintain the radioprotective capacity of CFU-S during retroviral infection

• Published in: Gene therapy Vol. 3; no. 9; p. 761
• Main Authors: Goncalves, F, Dubart, A, Lacout, C, Vainchenker, W, Duménil, D
• Format: Journal Article
• Language: English
• Published: England 01.09.1996
• Subjects: Animals; Anti-Bacterial Agents - pharmacology; Cell Adhesion; Cell Line; Coculture Techniques; Gene Transfer Techniques; Genetic Vectors - physiology; Gentamicins - pharmacology; Hematopoietic Stem Cell Transplantation; Hematopoietic Stem Cells - cytology; Kanamycin Kinase; Male; Mice; Mice, Inbred CBA; Phosphotransferases (Alcohol Group Acceptor) - genetics; Radiation Tolerance; Retroviridae - physiology; Spleen - cytology; Stromal Cells - physiology; Virus Integration
• ISSN: 0969-7128

Retroviral vectors provide an efficient means to introduce genes into hematopoietic stem cells. In order to develop retroviral infection protocols which preserve the radioprotective capacity of CFU-S, we designed a clonal hematopoietic reconstitution assay. In this assay, single CFU-S-derived derived colonies from bone marrow cells of 5-FU-treated mice were tested for their capacity to prevent radiation-induced mortality. Three parameters which may modify stem cell potential were tested in infection protocols using a retroviral vector containing the gene for neomycin resistance: (1) the partition of stem cells between the adherent and nonadherent fraction; (2) the replacement of the packaging cell line by a "competent' stromal cell line; and (3) the effects of G418 selection. All CFU-S having radioprotective capacity were found in the adherent fraction when the packaging cell line or the stromal cell line (MS-5) chosen for its capacity to maintain long-term bone marrow culture were used during the co-culture. The neo resistance gene was transduced into CFU-S with the same efficiency using co-culture with the packaging cell line or co-culture with the MS-5 cell line plus viral supernatant. However, in the presence of MS-5, a much higher proportion of CFU-S (70% versus 30%) had radioprotective properties, suggesting an important role for the stromal cells in the maintenance of hematopoietic reconstituting ability. Finally, G418 selection, even for a limited period (24 h), significantly decreased the radioprotective capacities of CFU-S (56% versus 18%). Subsequently, hematopoietic reconstitution by single CFU-S was quantified in recipient mice. The progeny of CFU-S were found at a significant level in the blood, spleen and bone marrow in 38% and 15% of mice, 1 and 3 months after transplantation, respectively. These results demonstrate that we have substantially improved the infection protocol. Under these conditions of infection, it is possible to conserve CFU-S properties and to transduce a gene into a stem cell with short-term hematopoietic reconstitution potential.