Kyle D. G. Saunders, Johanna von Gerichten, Rahul Deshpande, Matt Spick, Susan Bird, Giuseppe Schettino, Hannah Bolland, Anthony Whetton, Eirini Velliou and Melanie J. Bailey*,
{"title":"单细胞脂质组学的LC-MS实验室间研究揭示了x射线照射对胰腺癌细胞系及其旁观者的影响。","authors":"Kyle D. G. Saunders, Johanna von Gerichten, Rahul Deshpande, Matt Spick, Susan Bird, Giuseppe Schettino, Hannah Bolland, Anthony Whetton, Eirini Velliou and Melanie J. Bailey*, ","doi":"10.1021/acs.analchem.5c02010","DOIUrl":null,"url":null,"abstract":"<p >Live single-cell lipidomics by liquid chromatography mass spectrometry (LC-MS) is a nascent and rapidly growing field which can shed new light on infectious diseases, cancer, immunology, and drug delivery. There are now a growing number of laboratories that can isolate single cells and laboratories that can perform lipidomics analysis at correspondingly low sample volumes, but there is a lack of validation data. We have carried out the first interlaboratory LC-MS lipidomics experiment for single cells, aimed at filling this gap. We present a novel workflow to enable interlaboratory studies, comprising live-cell imaging and single-cell isolation, followed by freeze-drying, international shipping, reconstitution, and untargeted lipidomics analysis. We applied this methodology to reveal radiation-induced bystander effects in pancreatic cancer cells. X-ray irradiated cells and their bystanders sampled live 48 h postirradiation demonstrated reduced lipid abundance compared to controls, with distinct changes in molar ratios of several polyunsaturated lipids. This demonstrates for the first time that radiation can cause considerable cellular lipid remodelling, not only at the site of delivery. A striking similarity in lipid changes was observed between the two participating laboratories despite differences in sample preparation and analysis methods. Our results are further corroborated by live-cell imaging analysis of lipid droplets. This work serves as an important validation and demonstration of the nascent and rapidly growing field of live single-cell lipidomics.</p>","PeriodicalId":27,"journal":{"name":"Analytical Chemistry","volume":"97 25","pages":"13532–13541"},"PeriodicalIF":6.7000,"publicationDate":"2025-06-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://pubs.acs.org/doi/pdf/10.1021/acs.analchem.5c02010","citationCount":"0","resultStr":"{\"title\":\"Single-Cell Lipidomics by LC-MS Interlaboratory Study Reveals the Impact of X-ray Irradiation on a Pancreatic Cancer Cell Line and Its Bystanders\",\"authors\":\"Kyle D. G. Saunders, Johanna von Gerichten, Rahul Deshpande, Matt Spick, Susan Bird, Giuseppe Schettino, Hannah Bolland, Anthony Whetton, Eirini Velliou and Melanie J. Bailey*, \",\"doi\":\"10.1021/acs.analchem.5c02010\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >Live single-cell lipidomics by liquid chromatography mass spectrometry (LC-MS) is a nascent and rapidly growing field which can shed new light on infectious diseases, cancer, immunology, and drug delivery. There are now a growing number of laboratories that can isolate single cells and laboratories that can perform lipidomics analysis at correspondingly low sample volumes, but there is a lack of validation data. We have carried out the first interlaboratory LC-MS lipidomics experiment for single cells, aimed at filling this gap. We present a novel workflow to enable interlaboratory studies, comprising live-cell imaging and single-cell isolation, followed by freeze-drying, international shipping, reconstitution, and untargeted lipidomics analysis. We applied this methodology to reveal radiation-induced bystander effects in pancreatic cancer cells. X-ray irradiated cells and their bystanders sampled live 48 h postirradiation demonstrated reduced lipid abundance compared to controls, with distinct changes in molar ratios of several polyunsaturated lipids. This demonstrates for the first time that radiation can cause considerable cellular lipid remodelling, not only at the site of delivery. A striking similarity in lipid changes was observed between the two participating laboratories despite differences in sample preparation and analysis methods. Our results are further corroborated by live-cell imaging analysis of lipid droplets. This work serves as an important validation and demonstration of the nascent and rapidly growing field of live single-cell lipidomics.</p>\",\"PeriodicalId\":27,\"journal\":{\"name\":\"Analytical Chemistry\",\"volume\":\"97 25\",\"pages\":\"13532–13541\"},\"PeriodicalIF\":6.7000,\"publicationDate\":\"2025-06-17\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://pubs.acs.org/doi/pdf/10.1021/acs.analchem.5c02010\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Analytical Chemistry\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://pubs.acs.org/doi/10.1021/acs.analchem.5c02010\",\"RegionNum\":1,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, ANALYTICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Analytical Chemistry","FirstCategoryId":"92","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acs.analchem.5c02010","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, ANALYTICAL","Score":null,"Total":0}
Single-Cell Lipidomics by LC-MS Interlaboratory Study Reveals the Impact of X-ray Irradiation on a Pancreatic Cancer Cell Line and Its Bystanders
Live single-cell lipidomics by liquid chromatography mass spectrometry (LC-MS) is a nascent and rapidly growing field which can shed new light on infectious diseases, cancer, immunology, and drug delivery. There are now a growing number of laboratories that can isolate single cells and laboratories that can perform lipidomics analysis at correspondingly low sample volumes, but there is a lack of validation data. We have carried out the first interlaboratory LC-MS lipidomics experiment for single cells, aimed at filling this gap. We present a novel workflow to enable interlaboratory studies, comprising live-cell imaging and single-cell isolation, followed by freeze-drying, international shipping, reconstitution, and untargeted lipidomics analysis. We applied this methodology to reveal radiation-induced bystander effects in pancreatic cancer cells. X-ray irradiated cells and their bystanders sampled live 48 h postirradiation demonstrated reduced lipid abundance compared to controls, with distinct changes in molar ratios of several polyunsaturated lipids. This demonstrates for the first time that radiation can cause considerable cellular lipid remodelling, not only at the site of delivery. A striking similarity in lipid changes was observed between the two participating laboratories despite differences in sample preparation and analysis methods. Our results are further corroborated by live-cell imaging analysis of lipid droplets. This work serves as an important validation and demonstration of the nascent and rapidly growing field of live single-cell lipidomics.
期刊介绍:
Analytical Chemistry, a peer-reviewed research journal, focuses on disseminating new and original knowledge across all branches of analytical chemistry. Fundamental articles may explore general principles of chemical measurement science and need not directly address existing or potential analytical methodology. They can be entirely theoretical or report experimental results. Contributions may cover various phases of analytical operations, including sampling, bioanalysis, electrochemistry, mass spectrometry, microscale and nanoscale systems, environmental analysis, separations, spectroscopy, chemical reactions and selectivity, instrumentation, imaging, surface analysis, and data processing. Papers discussing known analytical methods should present a significant, original application of the method, a notable improvement, or results on an important analyte.