Cell Proliferation during the Maturation of Natural Killer Cells
- 1 April 1984
- journal article
- Published by Wiley in Scandinavian Journal of Immunology
- Vol. 19 (4), 379-383
- https://doi.org/10.1111/j.1365-3083.1984.tb00945.x
Abstract
The requirement for cell division during the maturation of natural killer (NK) cells was studied by following the appearance of donor-type NK cells in irradiated mice injected with bone marrow cells and by blocking the cell division at different times during this development. Irradiation (700 rad) or treatment with hydroxyurea (1 mg/g body weight, twice daily) of the recipient mice 7 days after the bone marrow cell inoculation inhibited the appearance of normal NK cell levels, suggesting that the NK cell progenitors are dividing cells. Blocking of the cell division in chimeras that had already developed high NK levels decreased the splenic NK activity, indicating the presence of a dividing NK cell population at this stage of maturation. These results are in accordance with the concept that mature NK cells are nondividing cells but are derived from actively proliferating progenitors in the bone marrow, and some of the first NK cells appearing in the spleen from the bone marrow can still be dividing.Keywords
This publication has 6 references indexed in Scilit:
- Decline of Natural Killer Cell Activity in Sublethally Irradiated Mice2JNCI Journal of the National Cancer Institute, 1978
- Natural cell‐mediated cytotoxicity in rats. III. Effects of immunopharmacologic treatments on natural reactivity and on reactivity augmented by polyinosinic‐polycytidylic acidInternational Journal of Cancer, 1978
- Published by Wiley ,1977
- Generation of natural killer cells: an autonomous function of the bone marrow.The Journal of Experimental Medicine, 1977
- „Natural”︁ killer cells in the mouse. I. Cytotoxic cells with specificity for mouse Moloney leukemia cells. Specificity and distribution according to genotypeEuropean Journal of Immunology, 1975
- Inducers of interferon and host resistance. II. Multistranded synthetic polynucleotide complexes.Proceedings of the National Academy of Sciences, 1967