The involvement of the 18kDa translocator protein (TSPO), a marker of neuroinflammation, in Alzheimer's disease (AD) remains controversial. In the present report, we used [125I]-CLINDE, a SPECT TSPO radiotracer never before used in AD, and we investigated the relationship between TSPO and amyloid plaque density (using [125I]-DRM106) in a triple transgenic mouse model of AD (3xTgAD, APPSWE, PS1M146V and TauP301L). Our results show that TSPO increases appear before those of amyloid deposits. Moreover, the different parts of the hippocampus are differentially affected. Indeed, for both TSPO and amyloid, the subiculum is affected earlier and the ventral hippocampus later than the dorsal hippocampus. In the subiculum and the dorsal hippocampus of 3xTgAD mice, a positive correlation between TSPO and of amyloid deposit levels is observed. This data supports the hypothesis that TSPO could be used as a predictive marker of amyloid pathology. In addition, our immunohistochemical data shows a segregation of TSPO in the hippocampus and immunofluorescence imaging revealed a mainly microglial origin of the TSPO expression. Thus, imaging TSPO with CLINDE may be a good alternative to PET radiotracers.

译文

18kDa转运蛋白 (TSPO) (神经炎症的标志物) 在阿尔茨海默氏病 (AD) 中的参与仍存在争议。在本报告中,我们使用了 [125I]-CLINDE,这是一种以前从未在AD中使用过的SPECT TSPO放射性示踪剂,并且我们在AD的三重转基因小鼠模型中研究了TSPO与淀粉样斑块密度之间的关系 (使用 [125I]-DRM106) (3xTgAD,APPSWE,PS1M146V和TauP301L)。我们的结果表明,TSPO增加出现在淀粉样蛋白沉积之前。此外,海马的不同部分受到不同程度的影响。实际上,对于TSPO和淀粉样蛋白,下丘脑比背侧海马更早受到影响,腹侧海马更晚。在3xtgad小鼠的下丘脑和背侧海马中,观察到TSPO与淀粉样蛋白沉积水平呈正相关。该数据支持以下假设: TSPO可以用作淀粉样蛋白病理的预测标记。此外,我们的免疫组织化学数据显示海马中TSPO的分离,免疫荧光成像显示TSPO表达的主要是小胶质细胞起源。因此,用CLINDE对TSPO进行成像可能是PET放射性示踪剂的良好替代品。

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