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Papers In Press, published online ahead of print September 1, 2009 J. Lipid Res., doi:10.1194/jlr.M900047-JLR200
Journal of Lipid Research, Vol. 50, 1776-1788, September 2009 Visualization of the cell-selective distribution of PUFA-containing phosphatidylcholines in mouse brain by imaging mass spectrometry[S]
* Department of Bioscience and Biotechnology, Tokyo Institute of Technology, 4259 Nagatsuta-cho, Midori-ku, Yokohama, Kanagawa 226-8501, Japan
1 To whom correspondence should be addressed. e-mail: setou{at}hama-med.ac.jp Previous studies have shown that MALDI-imaging mass spectrometry (IMS) can be used to visualize the distribution of various biomolecules, especially lipids, in the cells and tissues. In this study, we report the cell-selective distribution of PUFA-containing glycerophospholipids (GPLs) in the mouse brain. We established a practical experimental procedure for the IMS of GPLs. We demonstrated that optimization of the composition of the matrix solution and spectrum normalization to the total ion current (TIC) is critical. Using our procedure, we simultaneously differentiated and visualized the localizations of specific molecular species of GPLs in mouse brain sections. The results showed that PUFA-containing phosphatidylcholines (PCs) were distributed in a cell-selective manner: arachidonic acid- and docosahexaenoic acid-containing PCs were seen in the hippocampal neurons and cerebellar Purkinje cells, respectively. Furthermore, these characteristic localizations of PUFA-PCs were formed during neuronal maturation. The phenomenon of brain cell-selective production of specific PUFA-GPLs will help elucidate the potential physiological functions of PUFAs in specific brain regions.
Supplementary key words MALDI imaging MS LC ESI-MS/MS phospholipids development Abbreviations: AA, arachidonic acid; DHA, docosahexaenoic acid; DHB, dihydroxybenzoic acid; GPL, glycerol phospholipid; IMS, imaging mass spectrometry; ITO, indium-tin-oxide; PC, phosphatidylcholine; PCA, principle component analysis; PLA2, phospholipase A2; QIT, quadrupole ion trap; SIMS, secondary IMS; TIC, total ion current; TOF, time-of-flight
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