Visualization of Phospholipid Synthesis on Tissue Sections Using Functional Mass Spectrometry Imaging

被引:0
|
作者
Iwama, Taiga [1 ]
Kano, Kuniyuki [1 ]
Kawana, Hiroki [1 ,2 ]
Shindou, Hideo [3 ,4 ]
Shimizu, Takao [5 ,6 ]
Kono, Nozomu [1 ]
Aoki, Junken [1 ]
机构
[1] Univ Tokyo, Grad Sch Pharmaceut Sci, Dept Hlth Chem, Tokyo 1130033, Japan
[2] Nara Inst Sci & Technol, Grad Sch Sci & Technol, Div Biol Sci, Nara 6300192, Japan
[3] Natl Ctr Global Hlth & Med, Dept Lipid Life Sci, Tokyo 1628655, Japan
[4] Univ Tokyo, Grad Sch Med, Dept Med Lipid Sci, Tokyo 1130033, Japan
[5] Natl Ctr Global Hlth & Med, Dept Lipid Signaling, Tokyo 1628655, Japan
[6] Inst Microbial Chem, Tokyo 1410021, Japan
基金
日本学术振兴会; 日本科学技术振兴机构;
关键词
ACYL-COA; LIVER; ACYLTRANSFERASE; MITOCHONDRIAL; METABOLISM; PURIFICATION; EXPRESSION;
D O I
10.1021/acs.analchem.4c01219
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Functional mass spectrometry imaging (fMSI) is a potent tool for elucidating the spatial distribution of enzyme activities in tissues at high resolution. In this study, we applied fMSI to probe the intricate biosynthesis of phospholipids, which exist as thousands of molecular species in tissues and exhibit a unique distribution specific to cell type. By using deuterium- and C-13-labeled substrates, we visualized the activities of key enzymes involved in phospholipid synthesis, including glycerol 3-phosphate acyltransferase (GPAT), lysophosphatidic acid acyltransferases (LPAAT), lysophospholipid acyltransferases (LPLAT), and long-chain acyl-CoA synthetase (ACSL). Additionally, we were able to visualize a two-step sequential enzyme reaction involving ACSL and LPLAT. This novel approach unveiled significant variations in enzyme activity distribution depending on the type of fatty acids used as substrates. It will also help to reveal the mechanisms underlying the formation of numerous phospholipid species.
引用
收藏
页码:11771 / 11779
页数:9
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