Effect of quinolinic acid on human astrocytes morphology and functions: implications in Alzheimer's disease.

Effect of quinolinic acid on human astrocytes morphology and functions: implications in Alzheimer's disease.
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DOI:
10.1186/1742-2094-6-36
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发表时间:
2009-12-10
影响因子:
9.3
通讯作者:
Guillemin GJ
Guillemin GJ
中科院分区:
医学1区
文献类型:
--
作者:
Ting KK;Brew BJ;Guillemin GJ

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The excitotoxin quinolinic acid (QUIN) is synthesized through the kynurenine pathway (KP) by activated monocyte lineage cells. QUIN is likely to play a role in the pathogenesis of several major neuroinflammatory diseases including Alzheimer's disease (AD). The presence of reactive astrocytes, astrogliosis, increased oxidative stress and inflammatory cytokines are important pathological hallmarks of AD. We assessed the stimulatory effects of QUIN at low physiological to high excitotoxic concentrations in comparison with the cytokines commonly associated with AD including IFN-γ and TNF-α on primary human astrocytes. We found that QUIN induces IL-1β expression, a key mediator in AD pathogenesis, in human astrocytes. We also explored the effect of QUIN on astrocyte morphology and functions. At low concentrations, QUIN treatment induced concomitantly a marked increase in glial fibrillary acid protein levels and reduction in vimentin levels compared to controls; features consistent with astrogliosis. At pathophysiological concentrations QUIN induced a switch between structural protein expressions in a dose dependent manner, increasing VIM and concomitantly decreasing GFAP expression. Glutamine synthetase (GS) activity was used as a functional metabolic test for astrocytes. We found a significant dose-dependent reduction in GS activity following QUIN treatment. All together, this study showed that QUIN is an important factor for astroglial activation, dysregulation and cell death with potential relevance to AD and other neuroinflammatory diseases.
DOI: 10.1100/tsw.2001.107
发表时间: 2001
影响因子: --
作者:
Minagar A;Shapshak P;Heyes M;Sheremata WA;Fujimara R;Ownby R;Goodkin K;Eisdorfer K
通讯作者: Eisdorfer K
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期刊: BRAIN RESEARCH
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通讯作者: Brew, BJ