Infection of bone marrow cells in vitro with FLV: Effects on stem cell proliferation, differentiation and leukemogenic capacity
Autor: | T.M. Dexter, D. Scott, Natalie Teich |
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Rok vydání: | 1977 |
Předmět: |
viruses
Biology General Biochemistry Genetics and Molecular Biology Mice hemic and lymphatic diseases Precursor cell Murine leukemia virus Cell Adhesion medicine Animals Dimethyl Sulfoxide Induced pluripotent stem cell Erythropoietin Cells Cultured Leukemia Experimental Friend virus Temperature Hematopoietic Stem Cells biology.organism_classification Virology Clone Cells Friend murine leukemia virus Hematopoiesis Haematopoiesis medicine.anatomical_structure Helper virus Bone marrow Moloney murine leukemia virus Stem cell Cell Division |
Zdroj: | Cell. 12:355-364 |
ISSN: | 0092-8674 |
DOI: | 10.1016/0092-8674(77)90111-8 |
Popis: | Long-term cultures of proliferating hematopoietic stem cells derived from bone marrow permit the study of the interaction between murine leukemia virus (MuLV) infection and the proliferation and differentiation of stem cells. We have used this system to analyze the replication of different biological variants of MuLV in bone marrow cells; the effect of MuLV infection upon pluripotent stem cell (CFU-S) proliferation; and the effect of MuLV on differentiation of CFU-S along different hematopoietic pathways. Two MuLV variants were studied in detail: the Moloney strain of lymphatic leukemia virus (Mol-MuLV) and the erythroleukemic Friend virus complex (FLV) consisting of the lymphoid leukemia helper virus and the defective spleen focus-forming virus (SFFV). Mol-MuLV and its sarcoma virus pseudotype, MSV(Mol-MuLV), replicate efficiently in the bone marrow cultures; however, CFU-S are lost more readily than in uninfected cultures, and the cultures are soon represented by a majority population of mononuclear macrophages. On the other hand, infection with FLV produces a prolonged survival of the spleen colony-forming cells, CFU-S, and CFU-C (the committed granulocytic precursor cells). Production of erythroleukemogenic SFFV is maintained in these cultures for more than 40 weeks. No erythroblastic differentiation was observed in vitro, however, neither erythroblast precursor cells (CFU-E) nor hemoglobin-producing cells could be detected. This suggests that the target cell for FLV is an earlier precursor cell. |
Databáze: | OpenAIRE |
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