The structure and function of pardaxin

被引:0
作者
Lazarovici, P [1 ]
机构
[1] Hebrew Univ Jerusalem, Dept Pharmacol & Expt Therapeut, Sch Pharm, Fac Med, IL-91120 Jerusalem, Israel
来源
JOURNAL OF TOXICOLOGY-TOXIN REVIEWS | 2002年 / 21卷 / 04期
关键词
pardaxin; neurotoxin; pore; structure; tool; neurotransmitter release; calcium; arachidonic acid; PIA2; MAPK; cell death; signal transduction;
D O I
暂无
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
Pardaxins are polypeptide pore-forming neurotoxins that alter cell plasma membrane permeability by packaging of the hydrophobic, amphipathic alpha-helices and assembly in the plasma membrane in oligomeric, poorly selective channels. At subcytotoxic concentrations, these small lesions in the plasma membrane induce a sustained increase in intracellular calcium activation, stimulation of the arachidonic acid cascade and massive release of neurotransmitters. These crucial events are further amplified by cascades of cellular signaling, due to the release of local mediators (prostaglandins) and/or neurotransmitters (dopamine) and modifications of intracellular enzymes, ion channels and receptor activities. The end result is a lethal hit to the signal transduction machinery of the attacked cell, resulting in cell death. Elucidation of the neuronal signal transduction pathways affected by pardaxin could provide a new understanding of synaptic transmission and new targets for therapy of patients affected by neurotoxins.
引用
收藏
页码:391 / 421
页数:31
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