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24S-Hydroxycholesterol Correlates With Tau and Is Increased in Cerebrospinal Fluid in Parkinsons Disease and Corticobasal Syndrome

机译:24S-羟基胆固醇与Tau相关并且在帕金森氏病和皮质基底肌综合征中脑脊液中的含量增加

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摘要

24S-hydroxycholesterol (24OHC) and Tau are produced in neuronal cells and neurodegeneration leads to increased flux of both of them into cerebrospinal fluid (CSF). In the present study, CSF levels of 24OHC and 27S-hydroxycholesterol (27OHC) along with those of Tau, P-Thr181-Tau and Aβ42 were measured in patients with early Parkinson's disease (PD), Corticobasal syndrome (CBS), Corticobasal Degeneration (CBD), and controls. Using mouse models with increased or no formation of Tau protein and increased production of 24OHC, we have also tested the hypothesis that there is a direct association between neuronal turnover of 24OHC and Tau. The levels of 24OHC are increased, at a group level, in patients with PD or CBS. We found significant correlations between levels of 24OHC and Tau or P-Thr181-Tau in CSF from patients with PD, CBS or CBD. There were no similar correlations between 24OHC and Aβ42 in CSF from these patients. The neuronal levels of 24OHC were not altered in Tau knockout or Tau overexpressing mice. Vice versa, Tau species levels were not changed in Cyp46 overexpressing mice with increased neuronal levels of 24OHC. We conclude that the strongly correlative fluxes of 24OHC and Tau from neuronal cells to CSF are likely to be secondary to neurodegeneration and not due to direct interaction between the two factors. We suggest that this high correlation reflects a rapid neurodegeneration of specific neuronal subtypes with simultaneous release of 24OHC and Tau into the CSF.
机译:24S-羟基胆固醇(24OHC)和Tau在神经元细胞中产生,神经退行性变导致两者进入脑脊液(CSF)的流量增加。在本研究中,测定了帕金森氏病(PD),早期皮质肾上腺皮质激素患者的24OHC和27S-羟基胆固醇(27OHC)的脑脊液水平以及Tau,P-Thr 181 -Tau和Aβ42的水平综合征(CBS),皮质基底变性(CBD)和对照。使用具有增加的Tau蛋白形成或没有形成Tau蛋白和增加的24OHC产量的小鼠模型,我们还测试了以下假设:24OHC的神经元转换与Tau之间存在直接关联。 PD或CBS患者的24OHC水平以组水平增加。我们发现,PD,CBS或CBD患者的脑脊液中24OHC水平与Tau或P-Thr 181 -Tau含量之间存在显着相关性。这些患者的脑脊液中24OHC和Aβ42之间没有相似的相关性。 Tau基因敲除或Tau基因过表达的小鼠中24OHC的神经元水平没有改变。反之亦然,在神经元水平24OHC升高的Cyp46过表达小鼠中,Tau物种水平没有改变。我们得出结论,从神经元细胞到CSF的24OHC和Tau的强相关通量可能是继发于神经退行性病变的,而不是由于这两个因素之间的直接相互作用。我们建议,这种高度相关性反映了特定神经元亚型的快速神经变性,同时将24OHC和Tau释放到CSF中。

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