TY - JOUR
T1 - Radioresistance of culture-induced augmented natural killer-like activity
AU - Brovall, Charlotte
AU - Levitz, Stuart M.
AU - Ellner, Jerrold J.
AU - Schacter, Bernice
PY - 1983
Y1 - 1983
N2 - Human NK activity is radiosensitive under the control of X-linked genes. We have evaluated the expression of these genes in other forms of cellular cytotoxicity. The NK radioresistant and radiosensitive phenotype is expressed in ADCC. Specific cellular cytotoxicity, generated in a MLC with a radiosensitive donor as responder, was radioresistant, NK-like activity recruited from nonadherent cells of radiosensitive subjects stimulated with allogeneic cells, mitogens (PHA, Con A or PWM), or recall antigens (TT or PPD) was radioresistant. The acquisition of radioresistance was relatively rapid, beginning within 24 hr after exposure to PHA, prior to detectable proliferation. Radioresistance of MLR augmented NK-like activity was maximal 3 days after initiation of the culture. MLR augmented NK-like activity was spared by the immunosuppressive polypeptide antibiotic CsA at doses up to 1 μm/ml. CsA did, however, reduce acquisition of radioresistance by the NK-like activity at doses above 0.01 μgm/ml, a concentration which does not inhibit uptake of 3H-thymidine but does reduce the level of specific CML. These data suggest that mitogens and antigens, including allogeneic cells, are recruiting radioresistant NK-like activity which can be distinguished from the radiosensitive spontaneous NK activity of the cell donor. Further, in the MLR, both radiosensitive and radioresistant NK-like activity may be recruited.
AB - Human NK activity is radiosensitive under the control of X-linked genes. We have evaluated the expression of these genes in other forms of cellular cytotoxicity. The NK radioresistant and radiosensitive phenotype is expressed in ADCC. Specific cellular cytotoxicity, generated in a MLC with a radiosensitive donor as responder, was radioresistant, NK-like activity recruited from nonadherent cells of radiosensitive subjects stimulated with allogeneic cells, mitogens (PHA, Con A or PWM), or recall antigens (TT or PPD) was radioresistant. The acquisition of radioresistance was relatively rapid, beginning within 24 hr after exposure to PHA, prior to detectable proliferation. Radioresistance of MLR augmented NK-like activity was maximal 3 days after initiation of the culture. MLR augmented NK-like activity was spared by the immunosuppressive polypeptide antibiotic CsA at doses up to 1 μm/ml. CsA did, however, reduce acquisition of radioresistance by the NK-like activity at doses above 0.01 μgm/ml, a concentration which does not inhibit uptake of 3H-thymidine but does reduce the level of specific CML. These data suggest that mitogens and antigens, including allogeneic cells, are recruiting radioresistant NK-like activity which can be distinguished from the radiosensitive spontaneous NK activity of the cell donor. Further, in the MLR, both radiosensitive and radioresistant NK-like activity may be recruited.
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U2 - 10.1016/S0198-8859(83)80003-2
DO - 10.1016/S0198-8859(83)80003-2
M3 - Article
C2 - 6192119
AN - SCOPUS:0020964748
SN - 0198-8859
VL - 7
SP - 151
EP - 162
JO - Human Immunology
JF - Human Immunology
IS - 3
ER -