Department of Cellular and Molecular Anatomy, Hamamatsu University School of Medicine, 1-20-1 Handayama, Chuo-ku, Hamamatsu, Shizuoka 431-3192, Japan.
Preppers Co., Ltd., Hamamatsu University School of Medicine, 1-20-1 Handayama, Chuo-ku, Hamamatsu, Shizuoka 431-3192, Japan.
J Am Soc Mass Spectrom. 2024 Jun 5;35(6):1227-1236. doi: 10.1021/jasms.4c00045. Epub 2024 May 22.
Cholesterol is a primary lipid molecule in the brain that contains one-fourth of the total body cholesterol. Abnormal cholesterol homeostasis is associated with neurodegenerative disorders. Mass spectrometry imaging (MSI) technique is a powerful tool for studying lipidomics and metabolomics. Among the MSI techniques, desorption electrospray ionization-MSI (DESI-MSI) has been used advantageously to study brain lipidomics due to its soft and ambient ionization nature. However, brain cholesterol is poorly ionized. To this end, we have developed a new method for detecting brain cholesterol by DESI-MSI using low-temperature plasma (LTP) pretreatment as an ionization enhancement. In this method, the brain sections were treated with LTP for 1 and 2 min prior to DESI-MSI analyses. Interestingly, the MS signal intensity of cholesterol (at / 369.35 [M + H - HO]) was more than 2-fold higher in the 1 min LTP-treated brain section compared to the untreated section. In addition, we detected cholesterol, more specifically excluding isomers by targeted-DESI-MSI in multiple reaction monitoring (MRM) mode and similar results were observed: the signal intensity of each cholesterol transition (/ 369.4 → 95.1, 109.1, 135.1, 147.1, and 161.1) was increased by more than 2-fold due to 1 min LTP treatment. Cholesterol showed characteristic distributions in the fiber tract region, including the corpus callosum and anterior commissure, anterior part of the brain where LTP markedly ( < 0.001) enhanced the cholesterol intensity. In addition, the distributions of some unknown analytes were exclusively detected in the LTP-treated section. Our study revealed LTP pretreatment as a potential strategy to ionize molecules that show poor ionization efficiency in the MSI technique.
胆固醇是大脑中主要的脂质分子,占人体总胆固醇的四分之一。胆固醇代谢异常与神经退行性疾病有关。质谱成像(MSI)技术是研究脂质组学和代谢组学的有力工具。在 MSI 技术中,解吸电喷雾电离-MS(DESI-MS)由于其软电离和环境电离的特性,已被用于研究脑脂质组学。然而,大脑中的胆固醇电离效率较差。为此,我们开发了一种使用低温等离子体(LTP)预处理作为离子增强的 DESI-MSI 检测大脑胆固醇的新方法。在该方法中,在进行 DESI-MSI 分析之前,将脑切片用 LTP 处理 1 分钟和 2 分钟。有趣的是,与未经处理的切片相比,在 1 分钟 LTP 处理的脑切片中胆固醇(/ 369.35 [M + H - HO])的 MS 信号强度提高了 2 倍以上。此外,我们通过靶向-DESI-MSI 在多重反应监测(MRM)模式下检测胆固醇,更具体地排除异构体,观察到类似的结果:由于 1 分钟 LTP 处理,每个胆固醇跃迁的信号强度(/ 369.4→95.1、109.1、135.1、147.1 和 161.1)增加了 2 倍以上。胆固醇在纤维束区域呈现出特征性分布,包括胼胝体和前连合,在前脑区域,LTP 显著(<0.001)增强了胆固醇强度。此外,一些未知分析物的分布仅在 LTP 处理的切片中检测到。我们的研究表明,LTP 预处理是一种潜在的策略,可以使 MSI 技术中电离效率较低的分子电离。