Role of activated astrocytes in neuronal damage: Potential links to HIV-1-associated dementia

被引:64
|
作者
Deshpande, M
Zheng, JL
Borgmann, K
Persidsky, R
Wu, L
Schellpeper, C
Ghorpade, A
机构
[1] Univ Nebraska, Med Ctr, Lab Cellular Neuroimmunol, Omaha, NE 68198 USA
[2] Univ Nebraska, Med Ctr, Lab Neurotoxicol, Ctr Neurovirol & Neurodegenerat Disorders,Dept Ph, Omaha, NE 68198 USA
[3] Univ Nebraska, Med Ctr, Dept Pathol & Microbiol, Omaha, NE 68198 USA
[4] Univ Nebraska, Med Ctr, Dept Biochem & Mol Biol, Omaha, NE 68198 USA
关键词
HIV-1-associated dementia (HAD); astrocyte; apoptosis; glial inflammation; neurodegeneration; IL-1 beta activation; Fas ligand (FasL); neurotoxicity;
D O I
10.1007/BF03036448
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
HIV-1-associated dementia (HAD) is an important complication of HIV-1 infection. Reactive astrogliosis is a key pathological feature in HAD brains and in other central nervous system (CNS) diseases. Activated astroglia may play a critical role in CNS inflammatory diseases such as HAD. In order to test the hypothesis that activated astrocytes cause neuronal injury, we stimulated primary human fetal astrocytes with HAD-relevant pro-inflammatory cytokine IL-1 beta. IL-1 beta-activated astrocytes induced apoptosis and significant changes in metabolic activity in primary human neurons. An FITC-conjugated pan-caspase inhibitor peptide FITC-VAD-FMK was used for confirming caspase activation in neurons. IL-1 beta activation enhanced the expression of death protein FasL in astrocytes, suggesting that FasL is one of the potential factors responsible for neurotoxicity observed in HAD and other CNS diseases involving glial inflammation. Our data presented here add to the developing picture of role of activated glia in HAD pathogenesis.
引用
收藏
页码:183 / 192
页数:10
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