The role of calcium in transducing the signal for interleukin-1 (IL-1) secr
etion was examined in the MQ-NCSU chicken macrophage cell line. Cells were
maintained in RPMI 1640 medium supplemented with 5% chicken serum and antib
iotic-antimycotic solution at 40 C and 5% CO2. The effects of stimulation w
ith Lipopolysaccharide (LPS), calcium ionophore A23187, or a combination of
both on IL-1 secretion were examined. Calcium ionophore A23187 did not rep
lace LPS in MQ-NCSU stimulation but the LPS + A23187 combination stimulated
more IL-1 than ionophore alone in these cells. The combination of LPS and
ionophore did not increase IL-1 secretion above the levels observed with LP
S alone.
No synergistic effects between LPS and A23187 were evident. In order to dem
onstrate that IL-1 secretion by the MQ-NCSU cells is a calcium-dependent pr
ocess, ethylene glycol bis(beta-aminoethyl ether)N,N,N',N'-tetraacetic acid
(EGTA) was used to chelate free calcium in the cultures. Incorporation of
5 mM EGTA in the cultures lowered IL-1 stimulated by LPS + A23187 to contro
l levels. Addition of 5 mM CaCl2 to EGTA-suppressed cultures restored IL-1
secretion. These results indicate that the calcium ionophore, A23187, augme
nts IL-1 secretion by LPS-stimulated MQ-NCSU macrophages and that IL-1 secr
etion by these cells is a calcium-dependent process.