System Medicine, Steno Diabetes Center Copenhagen, Herlev, Denmark.
Institute of Pharmaceutical Sciences, Faculty of Life Sciences and Medicine, King's College London, Franklin-Wilkins Building, 150 Stamford Street, London, SE1 9NH, UK.
Mol Neurobiol. 2024 Apr;61(4):2021-2032. doi: 10.1007/s12035-023-03666-4. Epub 2023 Oct 16.
Cerebrospinal fluid (CSF) is a metabolically diverse biofluid and a key specimen for exploring biochemical changes in neurodegenerative diseases. Detecting lipid species in CSF using mass spectrometry (MS)-based techniques remains challenging because lipids are highly complex in structure, and their concentrations span over a broad dynamic range. This work aimed to develop a robust lipidomics and metabolomics method based on commonly used two-phase extraction systems from human CSF samples. Prioritizing lipid detection, biphasic extraction methods, Folch, Bligh and Dyer (B&D), Matyash, and acidified Folch and B&D (aFolch and aB&D) were compared using 150 μL of human CSF samples for the simultaneous extraction of lipids and metabolites with a wide range of polarity. Multiple chromatographical separation approaches, including reversed-phase liquid chromatography (RPLC), hydrophilic interaction liquid chromatography (HILIC), and gas chromatography (GC), were utilized to characterize human CSF metabolome. The aB&D method was found as the most reproducible technique (RSD < 15%) for lipid extraction. The aB&D and B&D yielded the highest peak intensities for targeted lipid internal standards and displayed superior extracting power for major endogenous lipid classes. A total of 674 unique metabolites with a wide polarity range were annotated in CSF using, combining RPLC-MS/MS lipidomics (n = 219), HILIC-MS/MS (n = 304), and GC-quadrupole time of flight (QTOF) MS (n = 151). Overall, our findings show that the aB&D extraction method provided suitable lipid coverage, reproducibility, and extraction efficiency for global lipidomics profiling of human CSF samples. In combination with RPLC-MS/MS lipidomics, complementary screening approaches enabled a comprehensive metabolite signature that can be employed in an array of clinical studies.
脑脊液(CSF)是一种代谢多样化的生物流体,是探索神经退行性疾病中生化变化的关键样本。使用基于质谱(MS)的技术检测 CSF 中的脂质种类仍然具有挑战性,因为脂质的结构非常复杂,其浓度跨越广泛的动态范围。本工作旨在开发一种基于常用两相提取系统从人 CSF 样本中提取脂质和代谢物的稳健脂质组学和代谢组学方法。优先考虑脂质检测,两相提取方法,Folch、Bligh 和 Dyer(B&D)、Matyash 和酸化 Folch 和 B&D(aFolch 和 aB&D),使用 150 μL 人 CSF 样本,同时提取具有广泛极性的脂质和代谢物。利用多种色谱分离方法,包括反相液相色谱(RPLC)、亲水相互作用液相色谱(HILIC)和气相色谱(GC),对人 CSF 代谢组进行了表征。aB&D 方法被发现是最可重复的脂质提取技术(RSD <15%)。aB&D 和 B&D 为靶向脂质内标物产生了最高的峰强度,并对主要内源性脂质类显示出优越的提取能力。使用 RPLC-MS/MS 脂质组学(n = 219)、HILIC-MS/MS(n = 304)和 GC-四极杆飞行时间(QTOF)MS(n = 151)相结合,在 CSF 中注释了具有广泛极性范围的 674 种独特代谢物。总体而言,我们的研究结果表明,aB&D 提取方法为全面的 CSF 脂质组学分析提供了合适的脂质覆盖度、重现性和提取效率。与 RPLC-MS/MS 脂质组学相结合,互补的筛选方法可以全面鉴定代谢物特征,可用于一系列临床研究。