Anti-apoptotic role of phospholipase D isozymes in the glutamate-induced cell death.
- Author:
Kyung Ok KIM
1
;
Kweon Haeng LEE
;
Young Hoon KIM
;
Seung Kiel PARK
;
Joong Soo HAN
Author Information
1. Institute of Biomedical Science, College of Medicine, Hanyang University, Seoul 133-791, Korea. jshan@hanyang.ac.kr
- Publication Type:Original Article ; Research Support, Non-U.S. Gov't
- Keywords:
apoptosis;
ceramides;
glutamic acid;
PC12 cells;
phospholipase D
- MeSH:
Animals;
Apoptosis/drug effects/*physiology;
Cell Survival/drug effects;
Ceramides/pharmacology;
Dose-Response Relationship, Drug;
Enzyme Activation;
Gene Expression Regulation, Enzymologic/drug effects;
Glutamic Acid/*toxicity;
Isoenzymes/drug effects/genetics/*metabolism;
Kinetics;
PC12 Cells;
Phospholipase D/chemistry/drug effects/genetics/*metabolism;
Rats;
Sphingolipids/metabolism
- From:Experimental & Molecular Medicine
2003;35(1):38-45
- CountryRepublic of Korea
- Language:English
-
Abstract:
Abstract Phospholipase D (PLD) plays an important role as an effector in a variety of physiological processes that reveal it to be a member of the signal transducing phospholipases. Recently, PLD2 was reported as a necessary intermediate in preventing apoptosis induced by hydrogen peroxide or hypoxia in rat pheochromocytoma (PC12) cells. The data presented here show that both PLD isozymes, PLD1 and PLD2 are also required in attenuating glutamate-induced cell death in PC12 cells. Treatment of PC12 cells with glutamate resulted in induction of apoptosis in these cells, which is accompanied by decreased PLD activity and increased ceramide concentration. Incubation of PC12 cells with exogenous C6-ceramide showed a time-dependent decrease of PLD activity. When cDNAs of PLD1 and PLD2 were transfected into PC12 cells respectively, overexpression of PLD1 or PLD2 resulted in inhibition of glutamate-induced apoptotic cell death. These data indicate that both PLD1 and PLD2 play a protective role against glutamate-induced cell death in PC12 cells.
