Long-term protection of hematopoiesis against the cytotoxic effects of multiple doses of nitrosourea by retrovirus-mediated expression of human O6-alkylguanine-DNA-alkyltransferase.
dc.contributor.author | Jelínek, Jaroslav | |
dc.contributor.author | Fairbairn, Leslie J | |
dc.contributor.author | Dexter, T Michael | |
dc.contributor.author | Rafferty, Joseph A | |
dc.contributor.author | Stocking, C | |
dc.contributor.author | Ostertag, W | |
dc.contributor.author | Margison, Geoffrey P | |
dc.date.accessioned | 2010-04-07T10:39:53Z | |
dc.date.available | 2010-04-07T10:39:53Z | |
dc.date.issued | 1996-03-01 | |
dc.identifier.citation | Long-term protection of hematopoiesis against the cytotoxic effects of multiple doses of nitrosourea by retrovirus-mediated expression of human O6-alkylguanine-DNA-alkyltransferase. 1996, 87 (5):1957-61 Blood | en |
dc.identifier.issn | 0006-4971 | |
dc.identifier.pmid | 8634444 | |
dc.identifier.uri | http://hdl.handle.net/10541/95845 | |
dc.description.abstract | A human O6-alkylguanine-DNA-alkyltransferase (ATase) cDNA-containing retrovirus was used to infect murine long-term primary bone marrow cultures. High levels of ATase expression were obtained, and colony-forming cells of the granulocyte-macrophage lineage from the cultures transduced with the human ATase retrovirus were three times more resistant to the alkylating agent, N-methyl-N-nitrosourea (MNU), than control cultures. Furthermore, expression of the human ATase protected long-term hematopoiesis, measured as the output of progenitor cells to the nonadherent fraction of the culture, against the cytotoxic effects of repeated exposures to MNU. These results clearly show that a human ATase cDNA-containing retrovirus can be used to infect long-term primary bone marrow cultures and that this attenuates their sensitivity to nitrosoureas. | |
dc.language.iso | en | en |
dc.subject | Haematopoiesis | en |
dc.subject | Haematopoietic Stem Cells | en |
dc.subject | Cultured Tumour Cells | en |
dc.subject.mesh | Animals | |
dc.subject.mesh | Antineoplastic Agents, Alkylating | |
dc.subject.mesh | Bone Marrow Cells | |
dc.subject.mesh | Cells, Cultured | |
dc.subject.mesh | DNA Damage | |
dc.subject.mesh | DNA Repair | |
dc.subject.mesh | DNA, Complementary | |
dc.subject.mesh | Genetic Vectors | |
dc.subject.mesh | Hematopoiesis | |
dc.subject.mesh | Hematopoietic Stem Cells | |
dc.subject.mesh | Humans | |
dc.subject.mesh | Methylnitrosourea | |
dc.subject.mesh | Methyltransferases | |
dc.subject.mesh | Mice | |
dc.subject.mesh | Mice, Inbred C57BL | |
dc.subject.mesh | Mice, Inbred DBA | |
dc.subject.mesh | O(6)-Methylguanine-DNA Methyltransferase | |
dc.subject.mesh | Recombinant Fusion Proteins | |
dc.subject.mesh | Retroviridae | |
dc.subject.mesh | Transfection | |
dc.subject.mesh | Tumor Cells, Cultured | |
dc.title | Long-term protection of hematopoiesis against the cytotoxic effects of multiple doses of nitrosourea by retrovirus-mediated expression of human O6-alkylguanine-DNA-alkyltransferase. | en |
dc.type | Article | en |
dc.contributor.department | CRC Department of Experimental Haematology, Paterson Institute for Cancer Research, Christie Hospital NHS Trust, Manchester, UK. | en |
dc.identifier.journal | Blood | en |
html.description.abstract | A human O6-alkylguanine-DNA-alkyltransferase (ATase) cDNA-containing retrovirus was used to infect murine long-term primary bone marrow cultures. High levels of ATase expression were obtained, and colony-forming cells of the granulocyte-macrophage lineage from the cultures transduced with the human ATase retrovirus were three times more resistant to the alkylating agent, N-methyl-N-nitrosourea (MNU), than control cultures. Furthermore, expression of the human ATase protected long-term hematopoiesis, measured as the output of progenitor cells to the nonadherent fraction of the culture, against the cytotoxic effects of repeated exposures to MNU. These results clearly show that a human ATase cDNA-containing retrovirus can be used to infect long-term primary bone marrow cultures and that this attenuates their sensitivity to nitrosoureas. |