Sekera Emily R, Rosas Lorena, Holbrook Joseph H, Angeles-Lopez Quetzalli D, Khaliullin Timur, Rojas Mauricio, Mora Ana L, Hummon Amanda B
Department of Chemistry and Biochemistry, The Ohio State University, Columbus, Ohio 43210 United States.
Department of Internal Medicine, Division of Pulmonary, Critical Care and Sleep Medicine, The Ohio State University, Columbus, Ohio 43210 United States.
J Am Soc Mass Spectrom. 2024 Dec 4;35(12):2815-2823. doi: 10.1021/jasms.4c00095. Epub 2024 Oct 30.
In this study, we evaluate lipids and select proteins in human lung fibroblasts (hLFs) to interrogate changes occurring due to aging and senescence. To study single cell populations, a comparison of cells adhered onto slides using poly-d-lysine versus centrifugal force deposition was first analyzed to determine whether specific alterations were observed between preparations. The poly-d-lysine approach was then utilized to interrogate the lipidome of the cell populations and further evaluate potential applications of the MALDI-immunohistochemistry (IHC) platform for single-cell-level analyses. Two protein markers of senescence, vimentin and p21, were both observed within the fibroblast populations and quantified. Lipidomic analysis of the fibroblasts found 12 lipids significantly altered because of replicative senescence, including fatty acids, such as stearic acid, and ceramide phosphoethanolamine species (CerPE). Similar to previous reports, alterations were detected in putative fatty acid building blocks, ceramides, among other lipid species. Altogether, our results reveal the ability to detect lipids implicated in senescence and show alterations to protein expression between normal and senescent fibroblast populations, including differences between young and aged cells. This report is the first time that the MALDI-IHC system has been utilized at a single-cell level to analyze both protein expression and lipid profiles in cultured cells, with a particular focus on changes associated with aging and senescence.
在本研究中,我们评估了人肺成纤维细胞(hLFs)中的脂质和特定蛋白质,以探究衰老和细胞衰老过程中发生的变化。为了研究单细胞群体,首先分析了使用聚-d-赖氨酸贴附在载玻片上的细胞与通过离心力沉积的细胞之间的差异,以确定在不同制备方法之间是否观察到特定变化。随后采用聚-d-赖氨酸方法来探究细胞群体的脂质组,并进一步评估基质辅助激光解吸电离免疫组织化学(MALDI-IHC)平台在单细胞水平分析中的潜在应用。在成纤维细胞群体中观察到衰老的两个蛋白质标志物波形蛋白和p21,并对其进行了定量分析。对成纤维细胞的脂质组分析发现,由于复制性衰老,有12种脂质发生了显著变化,包括脂肪酸(如硬脂酸)和神经酰胺磷酸乙醇胺种类(CerPE)。与之前的报道相似,在假定的脂肪酸构建块、神经酰胺以及其他脂质种类中检测到了变化。总之,我们的结果揭示了检测与衰老相关脂质的能力,并显示了正常和衰老成纤维细胞群体之间蛋白质表达的变化,包括年轻细胞和衰老细胞之间的差异。本报告首次在单细胞水平上利用MALDI-IHC系统分析培养细胞中的蛋白质表达和脂质谱,特别关注与衰老和细胞衰老相关的变化。