Mechanisms of PrionSc- and HIV-1 gp120 induced neuronal cell death

被引:0
|
作者
Schröder, HC
Perovic, S
Kavsan, V
Ushijima, H
Müller, WEG
机构
[1] Univ Mainz, Inst Physiol Chem, Angew Mol Biol Abt, D-55099 Mainz, Germany
[2] Ukrainian Acad Sci, Inst Mol Biol & Genet, Dept Biosynth Nucl Acids, UA-252627 Kiev, Ukraine
[3] Inst Publ Hlth, Minato Ku, Tokyo 108, Japan
关键词
prion protein; gp120; apoptosis; NMDA receptor; Bcl-2;
D O I
暂无
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
In vitro experiments revealed that the scrapie prion protein, PrPSc, as well as the PrP fragment PrP106-126, and the HIV-1 coat protein gp 120 induce apoptosis of rat cortical neurons. The toxic effect displayed by PrP and gp120 could be blocked by NMDA receptor antagonists. Treatment of neuronal cells with PrP106-126 resulted in a drop of intracellular glutathione level and changes in the level of Bcl-2. Evidence is presented that gp120 causes an activation of phospholipase A,, resulting in the increased release of arachidonic acid, which may in turn sensitize the NMDA receptor. (C) 1998 Inter Press, Inc.
引用
收藏
页码:683 / 688
页数:6
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