The role of glutamine (GLN) in the generation of lymphokine-activated
killer (LAK) cell activity was investigated. LAK cells were derived fr
om healthy donors and peripheral blood mononuclear cells (PBMC) were o
btained using either unseparated PMBC or DR- CD3- CD16+ CD56+ enriched
cells. PBMC were cultured for 6 or 10 days in medium supplemented wit
h recombinant interleukin-2 (rIL-2; 100 U/ml) in the presence of diffe
rent concentrations of GLN. K562 (natural killer-NK-sensitive targets)
, 1301 and U-937 (NK-resistant targets) cells were used as targets in
the cytotoxic assays. Furthermore, the limiting dilution (LD) culture
system was applied as an alternative to the bulk cell culture system.
It was found that GLN affects the lytic potential of cultured cells wh
ile the frequency of responding cells did not significantly differ bet
ween the compared cell cultures performed in the presence of different
amounts of GLN. Data on cell proliferation with IL-2 stimulation show
ed significant differences in cultures performed in the presence or ab
sence of GLN. The results of present investigation suggest a supportiv
e role of GLN in the generation of LAK cells. GLN deficit affects LAK
cell killing activity by limiting the number of generated effector cel
ls while acquisition of broad-range killing capacity was not affected.