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磷脂酶A2在与缺血和兴奋性毒性相关的脑细胞及组织损伤中的作用。

Roles of phospholipases A2 in brain cell and tissue injury associated with ischemia and excitotoxicity.

作者信息

Bonventre J V

机构信息

Massachusetts General Hospital, Department of Medicine, Harvard Medical School, Boston 02114, USA.

出版信息

J Lipid Mediat Cell Signal. 1997 Sep;17(1):71-9. doi: 10.1016/s0929-7855(97)00021-7.

Abstract

Phospholipase A2 (PLA2) activity is an important contributor to destructive cellular processes in the central nervous system. Two cytosolic forms of calcium dependent PLA2 have been characterized in the gerbil brain and the neuronal cultures from rat brain. PLA2 enzymatic activity in cell free extracts from cortical neuronal cultures is upregulated after cells are exposed to glutamate. Brief exposure to a calcium ionophore or phorbol 12-myristate 13-acetate (PMA) stably enhanced PLA2 activity. Stable activation of the two cytosolic forms of PLA2 occur prior to evidence of cell death and this activation is reversible. The larger molecular mass form was characterized as cPLA2. The smaller form (approximately 14 kDa) was distinct from Group I and II PLA2. Exposure to glutamate shifted the calcium activation curve of the smaller form to the left suggesting a novel mechanism of regulation of PLA2. Glutamate-induced stable enhancement of PLA2 activity, by processes involving calcium and protein kinase C activation, is a potential molecular switch likely mediating changes in synaptic function and contributing to excitotoxicity.

摘要

磷脂酶A2(PLA2)活性是中枢神经系统中破坏性细胞过程的一个重要促成因素。在沙鼠脑和大鼠脑神经元培养物中已鉴定出两种胞质形式的钙依赖性PLA2。在皮质神经元培养物的无细胞提取物中,细胞暴露于谷氨酸后,PLA2酶活性上调。短暂暴露于钙离子载体或佛波醇12 - 肉豆蔻酸酯13 - 乙酸酯(PMA)可稳定增强PLA2活性。两种胞质形式的PLA2的稳定激活发生在细胞死亡迹象出现之前,且这种激活是可逆的。较大分子量形式被鉴定为cPLA2。较小形式(约14 kDa)与I组和II组PLA2不同。暴露于谷氨酸使较小形式的钙激活曲线向左移动,提示PLA2的一种新的调节机制。通过涉及钙和蛋白激酶C激活的过程,谷氨酸诱导的PLA2活性稳定增强是一种潜在的分子开关,可能介导突触功能变化并导致兴奋性毒性。

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