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A Micro-Silicon Chip for in Vivo Cerebral Imprint in Monkey

机译:猴子体内脑烙印的微硅芯片

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摘要

Access to cerebral tissue is essential to better understand the molecular mechanisms associated with neurodegenerative diseases. In this study, we present, for the first time, a new tool designed to obtain molecular and cellular cerebral imprints in the striatum of anesthetized monkeys. The imprint is obtained during a spatially controlled interaction of a chemically modified micro-silicon chip with the brain tissue. Scanning electron and immunofluorescence microscopies showed homogeneous capture of cerebral tissue. Nano-liquid chromatography–tandem mass spectrometry (nano-LC-MS/MS) analysis of proteins harvested on the chip allowed the identification of 1158 different species of proteins. The gene expression profiles of mRNA extracted from the imprint tool showed great similarity to those obtained via the gold standard approach, which is based on post-mortem sections of the same nucleus. Functional analysis of the harvested molecules confirmed the spatially controlled capture of striatal proteins implicated in dopaminergic regulation. Finally, the behavioral monitoring and histological results establish the safety of obtaining repeated cerebral imprints in striatal regions. These results demonstrate the ability of our imprint tool to explore the molecular content of deep brain regions in vivo. They open the way to the molecular exploration of brain in animal models of neurological diseases and will provide complementary information to current data mainly restricted to post-mortem samples.
机译:进入脑组织对于更好地了解与神经退行性疾病相关的分子机制至关重要。在这项研究中,我们首次提出了一种新工具,旨在获得麻醉猴子纹状体中的分子和细胞脑烙印。在化学修饰的微硅芯片与大脑组织的空间受控相互作用期间获得印记。扫描电子和免疫荧光显微镜检查显示均捕获脑组织。纳米液相色谱-串联质谱(nano-LC-MS / MS)分析了芯片上收获的蛋白质,从而鉴定了1158种不同的蛋白质。从压印工具提取的mRNA的基因表达谱显示出与通过金标准方法获得的基因表达谱非常相似,该方法基于同一核的死后切片。对所收获分子的功能分析证实了与多巴胺能调节有关的纹状体蛋白的空间控制捕获。最后,行为监测和组织学结果建立了在纹状体区域获得重复脑印的安全性。这些结果证明了我们的印迹工具能够探索体内深部大脑区域的分子含量。它们为神经疾病动物模型中的大脑分子探索开辟了道路,并将为主要限于验尸样品的当前数据提供补充信息。

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