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Comprehensive proteomic profiling of plasma-derived Extracellular Vesicles from dementia with Lewy Bodies patients

机译:路易体患者痴呆血浆来源的细胞外囊泡的全面蛋白质组学分析

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摘要

Proteins and nucleic acids contained in extracellular vesicles (EVs) are considered a feasible source of putative biomarkers for physiological and pathological conditions. Within the nervous system, not only neurons but also other brain cells are able to produce EVs, which have been involved in their physiological processes and also in the development and course of several neurodegenerative diseases. Among these, dementia with Lewy bodies (DLB) is the second cause of dementia worldwide, though most cases are missed or misdiagnosed as Alzheimer’s disease (AD) due to the important clinical and pathological overlap between both diseases. In an attempt to find reliable biomarkers for DLB diagnosis, our group characterized the proteome of plasma-derived EVs from DLB patients compared to aged-matched healthy controls (HCs) using two different proteomic LC-MS/MS approaches. Remarkably, we found that gelsolin and butyrylcholinesterase were differentially identified between DLB and HCs. Further validation of these results using conventional ELISA techniques, and including an additional group of AD patients, pointed to decreased levels of gelsolin in plasma-EVs from DLB compared to HCs and to AD samples. Thus, gelsolin may be considered a possible biomarker for the differentiation between DLB and AD.
机译:细胞外囊泡(EVs)中包含的蛋白质和核酸被认为是生理和病理状况的假定生物标志物的可行来源。在神经系统内,不仅神经元而且其他脑细胞也能够产生EV,这些EV参与了它们的生理过程以及几种神经退行性疾病的发展和进程。其中,路易体痴呆(DLB)是全球范围内痴呆的第二个原因,尽管由于两种疾病之间重要的临床和病理重叠,大多数病例被遗漏或误诊为阿尔茨海默氏病(AD)。为了寻找可靠的DLB诊断生物标志物,我们的研究小组使用两种不同的蛋白质组学LC-MS / MS方法,与年龄匹配的健康对照(HCs)相比,对DLB患者血浆来源的EV的蛋白质组进行了表征。值得注意的是,我们发现在DLB和HCs之间可以鉴别出凝溶胶蛋白和丁酰胆碱酯酶。使用常规ELISA技术对这些结果进行的进一步验证(包括另一组AD患者)指出,与HC和AD样品相比,来自DLB的血浆电动汽车中凝溶胶蛋白水平降低。因此,凝溶胶蛋白可以被认为是区分DLB和AD的可能的生物标记。

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