Improved ion detection sensitivity in mass spectrometry imaging using tapping-mode scanning probe electrospray ionization to visualize localized lipids in mouse testes

Mass spectrometry imaging (MSI) is a promising analytical method to visualize the distribution of lipids in biological tissues. To clarify the relationship between cellular distribution and lipid types in a tissue, it is crucial to achieve both an improvement in ion detection sensitivity and a reduction in the ionization area. We report methods for improving the efficiency of ion transfer to a mass spectrometer and miniaturizing the extraction area of a sample for tapping-mode scanning probe electrospray ionization (t-SPESI), atmospheric pressure sampling, and ionization methods. To verify the efficacy of the new t-SPESI measurement system, MSI was performed on mouse testes with a pixel size of 5 µm. Lipid images of the testes from wild-type (WT) and lysophospholipid acyltransferase 3 (LPLAT3) knockout mice revealed the characteristic distribution of docosahexaenoic acid-containing phospholipids (DHA-PLs). A comparison of the ion images obtained by MSI and optical images of the same tissues stained with hematoxylin and eosin suggested that the distribution of DHA-PLs was significantly altered by spermatogenesis in the WT mouse testes.

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Publication Details

Journal
Analytical and Bioanalytical Chemistry
Published
2024-11-21
DOI
https://doi.org/10.1007/s00216-024-05641-x
Citations
6
Primary Topic
Mass Spectrometry Techniques and Applications
Type
article
Field-Weighted Citation Impact
1.44

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article

Improved ion detection sensitivity in mass spectrometry imaging using tapping-mode scanning probe electrospray ionization to visualize localized lipids in mouse testes

Mengze Sun, Yoichi Otsuka, Makoto Yamada, Hideo Shindou et al.
6 citations
Analytical and Bioanalytical Chemistry
Mass Spectrometry Techniques and Applications
1.44
article

Improved ion detection sensitivity in mass spectrometry imaging using tapping-mode scanning probe electrospray ionization to visualize localized lipids in mouse testes

Mengze Sun, Yoichi Otsuka, Makoto Yamada, Hideo Shindou, Michisato Toyoda, Katsuyuki Nagata, Maki Okada, Tomomi Hashidate‐Yoshida, Motohito Goto
article en
6 citations

Abstract

Mass spectrometry imaging (MSI) is a promising analytical method to visualize the distribution of lipids in biological tissues. To clarify the relationship between cellular distribution and lipid types in a tissue, it is crucial to achieve both an improvement in ion detection sensitivity and a reduction in the ionization area. We report methods for improving the efficiency of ion transfer to a mass spectrometer and miniaturizing the extraction area of a sample for tapping-mode scanning probe electrospray ionization (t-SPESI), atmospheric pressure sampling, and ionization methods. To verify the efficacy of the new t-SPESI measurement system, MSI was performed on mouse testes with a pixel size of 5 µm. Lipid images of the testes from wild-type (WT) and lysophospholipid acyltransferase 3 (LPLAT3) knockout mice revealed the characteristic distribution of docosahexaenoic acid-containing phospholipids (DHA-PLs). A comparison of the ion images obtained by MSI and optical images of the same tissues stained with hematoxylin and eosin suggested that the distribution of DHA-PLs was significantly altered by spermatogenesis in the WT mouse testes.

Analytical and Bioanalytical ChemistryVol. 417(2)
Osaka University of Economics (JP), Central Institute for Experimental Animals (JP), National Center for Global Health and Medicine (JP), The University of Tokyo (JP), Shimadzu (Japan) (JP), The University of Osaka (JP)
Asahi Glass Foundation, Japan Agency for Medical Research and Development, National Center for Global Health and Medicine, Japan Health Research Promotion Bureau, Osaka University, Toyota Physical and Chemical Research Institute, Japan Society for the Promotion of Science, Precursory Research for Embryonic Science and Technology
Openalex Percentile: Top 19%
Mass Spectrometry Techniques and Applications
1.44
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