PHOSPHATIDYLSERINE SYNTHESIS IN GLIOMA C6 CELLS IS INHIBITED BY CA2-RETICULUM - EFFECTS OF 2,5-DI-TERT-BUTYLHYDROQUINONE AND THIMEROSAL( DEPLETION FROM THE ENDOPLASMIC)
M. Wiktorek et al., PHOSPHATIDYLSERINE SYNTHESIS IN GLIOMA C6 CELLS IS INHIBITED BY CA2-RETICULUM - EFFECTS OF 2,5-DI-TERT-BUTYLHYDROQUINONE AND THIMEROSAL( DEPLETION FROM THE ENDOPLASMIC), Biochemical and biophysical research communications, 224(3), 1996, pp. 645-650
The effects of 2,5-di-tertbutylhydroquinone (DBHQ) and thimerosal on p
hosphatidylserine synthesis by the base exchange reaction and on calci
um mobilization in intact glioma C6 cells were compared with that of t
hapsigargin, a selective inhibitor of the endoplasmic reticulum Ca2+-A
TPase. It has been found that all these agents inhibit phosphatidylser
ine synthesis by 70%, but their effectiveness are different. The data
show that this inhibition is caused by Ca2+ depletion of the endoplasm
ic reticulum, indicating that phosphatidylserine synthesis requires hi
gh concentration of Ca2+ within this structure. On this basis and on l
iterature data, a new model for the localization of the serine base ex
change enzyme in the endoplasmic reticulum membrane is proposed. (C) 1
996 Academic Press, Inc.