PHOSPHATIDYLSERINE SYNTHESIS IN GLIOMA C6 CELLS IS INHIBITED BY CA2-RETICULUM - EFFECTS OF 2,5-DI-TERT-BUTYLHYDROQUINONE AND THIMEROSAL( DEPLETION FROM THE ENDOPLASMIC)

Citation
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
Citations number
21
Categorie Soggetti
Biology,Biophysics
ISSN journal
0006291X
Volume
224
Issue
3
Year of publication
1996
Pages
645 - 650
Database
ISI
SICI code
0006-291X(1996)224:3<645:PSIGCC>2.0.ZU;2-X
Abstract
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.