Age-related decline in activation of JNK by TCR- and CD28-mediated signalsin murine T-lymphocytes

c-Jun N-terminal kinase (JNK) is activated when T-lymphocytes are stimulate d jointly through the T-cell receptor (TCR) and CD28, and it contributes to T-cell activation and IL-2 production through phosphorylation of transcrip tion factors, including c-Jun, We performed in vitro kinase assays on JNK i n CD4(+) T-cells, from young and old mice, activated by antibodies to CD3, CD4, and CD28, and found a similar to 2-fold decline in JNK activity at the peak of activation, but no significant change in the kinetics of stimulati on or in the steady-state expression of JNK, We found a similar decline in c-Jun phosphorylation in stimulated CD4(+) T-cells from old mice, suggestin g that JNK activation also declined with age in intact cells. Aging does no t, however, alter the level of Ras activation by anti-CD3/CD4 +/- anti-CD28 or change the level of Ras protein in CD4(+) cells, suggesting that the JN K defect is due to changes in the regulation of other upstream regulators. Our results suggest that a decline with age in JNK responses may contribute to the decline in proliferation and IL-2 production seen in CD4(+) T-cells from old mice. (C) 1999 Academic Press.