Lipid Alterations during Zebrafish Embryogenesis Revealed by Dynamic Mass Spectrometry Profiling with C=C Specificity.
Xu ZhaoJing ChenWeiying ZhangChengdui YangXiaoxiao MaSichun ZhangXinrong ZhangPublished in: Journal of the American Society for Mass Spectrometry (2019)
Lipids exert substantial influences on vertebrate embryogenesis, but their metabolic dynamics at detailed structural levels remains elusive, primarily owing to the lack of a tool capable of resolving their huge structural diversity. Herein, we present the first large-scale and spatiotemporal monitoring of unsaturated lipids with C=C specificity in single developing zebrafish embryos enabled by photochemical derivatization and tandem mass spectrometry (MS). The lipid isomer composition was found extremely stable in yolk throughout embryogenesis, while notable differences in ratios of C=C location (e.g., PC 16:0_16:1 (7) vs. 16:0_16:1 (9)) and fatty acyl composition isomers (e.g., PC 16:1_18:1 vs. 16:0_18:2) were unveiled between blastomeres and yolk from zygote to 4 h post fertilization (hpf). From 24 hpf onwards, lipid isomer compositions in embryo head and tail evolved distinctively with development, suggesting a meticulously regulated lipid remodeling essential for cell division and differentiation. This work has laid the foundation for functional studies of structurally defined lipids in vertebrate embryology.
Keyphrases
- fatty acid
- mass spectrometry
- tandem mass spectrometry
- liquid chromatography
- high performance liquid chromatography
- gas chromatography
- ultra high performance liquid chromatography
- simultaneous determination
- single cell
- ms ms
- high resolution mass spectrometry
- high resolution
- solid phase extraction
- multiple sclerosis
- gas chromatography mass spectrometry
- cell therapy
- stem cells
- mesenchymal stem cells
- bone marrow
- capillary electrophoresis
- pregnancy outcomes