Sc. Dreskin et al., PHOSPHOENOLPYRUVATE AND CREATINE-PHOSPHATE AUGMENT ATP AND MAGNESIUM-DEPENDENT, FC-EPSILON-RI-MEDIATED ACTIVATION OF PHOSPHOLIPASE-C IN RBLCELL GHOSTS, The Journal of immunology, 151(6), 1993, pp. 3199-3205
We have previously reported that FCepsilonRI-mediated activation of PL
C occurs in plasma membrane vesicles derived from RBL cells. This acti
vity is dependent on ATP and magnesium, and is greatly enhanced by the
addition of either PEP or CP. We undertook these studies to determine
whether these compounds augment FCepsilonRI-mediated activation of PL
C because of their ability to form ATP. The specific findings were 1)
the addition of increasing amounts of ATP to the ghost vesicles cannot
substitute for the combination of ATP and either PEP or CP; 2) the ad
dition of increasing amounts of ATP or a combination of ATP and either
PEP or CP results in similar levels of intravesicular ATP; 3) many me
tabolically related compounds have some activity to support receptor-m
ediated PI hydrolysis, but only PEP, CP, and 3-PG give a maximal signa
l; and 4) the inability of ATP alone to support optimal receptor-media
ted PI hydrolysis does not appear to be due to the accumulation of ADP
because ADP is only modestly inhibitory. Taken together, these data a
re evidence that augmentation of FcepsilonRI-mediated PI hydrolysis by
PEP and CP is not explained simply by the ability of these compounds
to generate intravesicular ATP.