Visualization of phosphatidylcholine, lysophosphatidylcholine and sphingomyelin in mouse tongue body by matrix-assisted laser desorption/ionization imaging mass spectrometry

被引:31
作者
Enomoto, Hirofumi [1 ]
Sugiura, Yuki [1 ]
Setou, Mitsutoshi [1 ]
Zaima, Nobuhiro [1 ]
机构
[1] Hamamatsu Univ Sch Med, Dept Mol Anat, Higashi Ku, Hamamatsu, Shizuoka 4313192, Japan
关键词
Imaging mass spectrometry; Mouse tongue body; Phosphatidylcholine; Lysophosphatidylcholine; Sphingomyelin; Matrix-assisted laser desorption/ionization; PHOSPHOLIPIDS; TISSUE; RAT; PURIFICATION; LIPIDOMICS; LIPIDS; BRAIN; TIME;
D O I
10.1007/s00216-011-4924-4
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The mammalian tongue is one of the most important organs during food uptake because it is helpful for mastication and swallowing. In addition, taste receptors are present on the surface of the tongue. Lipids are the second most abundant biomolecules after water in the tongue. Lipids such as phosphatidylcholine (PC), lysophosphatidylcholine (LPC) and sphingomyelin (SM) are considered to play fundamental roles in the mediation of cell signaling. Imaging mass spectrometry (IMS) is powerful tool for determining and visualizing the distribution of lipids across sections of dissected tissue. In this study, we identified and visualized the PC, LPC, and SM species in a mouse tongue body section with matrix-assisted laser desorption/ionization (MALDI)-IMS. The ion image constructed from the peaks revealed that docosahexaenoic acid (DHA)-containing PC, LPC, linoleic acid-containing PC and SM (d18:1/16:0), and oleic acid-containing PC were mainly distributed in muscle, connective tissue, stratified epithelium, and the peripheral nerve, respectively. Furthermore, the distribution of SM (d18:1/16:0) corresponded to the distribution of nerve tissue relating to taste in the stratified epithelium. This study represents the first visualization of PC, LPC and SM localization in the mouse tongue body.
引用
收藏
页码:1913 / 1921
页数:9
相关论文
共 36 条
  • [1] PURIFICATION OF AN ENZYME WITH LYSOPHOSPHOLIPASE ACTIVITY FROM RAT INTESTINAL-MUCOSA BY HYDROPHOBIC CHROMATOGRAPHY
    ALLENMARK, S
    SJODAHL, E
    SJODAHL, R
    TAGESSON, C
    [J]. PREPARATIVE BIOCHEMISTRY, 1980, 10 (04): : 463 - 471
  • [2] Positional analysis of triglycerides and phospholipids rich in long-chain polyunsaturated fatty acids
    Amate, L
    Ramírez, M
    Gil, A
    [J]. LIPIDS, 1999, 34 (08) : 865 - 871
  • [3] Mass spectral imaging and profiling of neuropeptides at the organ and cellular domains
    Chen, Ruibing
    Li, Lingjun
    [J]. ANALYTICAL AND BIOANALYTICAL CHEMISTRY, 2010, 397 (08) : 3185 - 3193
  • [4] Time, life ... and mass spectrometry - New techniques to address biological questions
    Costello, CE
    [J]. BIOPHYSICAL CHEMISTRY, 1997, 68 (1-3) : 173 - 188
  • [5] FOLCH J, 1957, J BIOL CHEM, V226, P497
  • [6] MALDI Imaging Mass Spectrometry
    Franck, Julien
    Arafah, Karim
    Elayed, Mohamed
    Bonnel, David
    Vergara, Daniele
    Jacquet, Amelie
    Vinatier, Denis
    Wisztorski, Maxence
    Day, Robert
    Fournier, Isabelle
    Salzet, Michel
    [J]. MOLECULAR & CELLULAR PROTEOMICS, 2009, 8 (09) : 2023 - 2033
  • [7] An update of MALDI-TOF mass spectrometry in lipid research
    Fuchs, Beate
    Suess, Rosmarie
    Schiller, Juergen
    [J]. PROGRESS IN LIPID RESEARCH, 2010, 49 (04) : 450 - 475
  • [8] FUTO T, 1989, J NEUROL SCI, V129, P97
  • [9] Shotgun lipidomics: Electrospray ionization mass spectrometric analysis and quantitation of cellular lipidomes directly from crude extracts of biological samples
    Han, XL
    Gross, RW
    [J]. MASS SPECTROMETRY REVIEWS, 2005, 24 (03) : 367 - 412
  • [10] Principles of bioactive lipid signalling: lessons from sphingolipids
    Hannun, Yusuf A.
    Obeid, Lina M.
    [J]. NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2008, 9 (02) : 139 - 150