We have previously shown that stimulation of B lymphocytes with calcium ion
ophores lead to the phosphorylation and enzymatic activation of ERK2. We ha
ve now determined that stimulation of human primary and Jurkat T lymphocyte
s with ionomycin also results in the activation of ERK1 and 2 as determined
by; shifts in the mobility of this enzyme on SDS-PACE gels, the binding of
an antibody that recognizes only the activated form of this enzyme, and in
creased ability to phosphorylate myelin basic protein (MBP). Another calciu
m ionophore, A23187, also induced activation of ERK1 and 2 in human primary
and Jurkat T lymphocytes demonstrating that this is a general effect of ca
lcium ionophores and is not limited to ionomycin. The activation of ERK1 an
d 2 by calcium ionophores was rapid, transient, and occurred in a dose-depe
ndent manner. Activation of ERK1 and 2 by increases in intracellular calciu
m were blocked by the MEK inhibitor PD98059. These data point to a new role
for calcium fluxes in T lymphocytes. (C) 1999 Elsevier Science Ltd. All ri
ghts reserved.