Evidence map›Paper›PMID 40369247›Full record

ArticleCommunications chemistry2025

Single-cell mass spectrometry imaging of lipids in HeLa cells via tapping-mode scanning probe electrospray ionization.

Yoichi Otsuka, Kazuya Kabayama, Ayane Miura, Masatomo Takahashi, Kosuke Hata, Yoshihiro Izumi, Takeshi Bamba, Koichi Fukase, Michisato Toyoda

Abstract read
In one paragraph

Article in Communications chemistry, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. New Analytical Technologies to Resolve, Interpret, and Understand Lipid Complexity.Annual review of analytical chemistry (Palo Alto, Calif.) · 2026
    Review
  5. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Yoichi OtsukaDepartment of Physics, Graduate School of Science, The University of Osaka, Toyonaka, Osaka, Japan. otsuka@phys.sci.osaka-u.ac.jp.ORCID http://orcid.org/0000-0003-2304-6637
Kazuya KabayamaDepartment of Chemistry, Graduate School of Science, The University of Osaka, Toyonaka, Osaka, Japan.ORCID http://orcid.org/0000-0002-7583-5454
Ayane MiuraDepartment of Chemistry, Graduate School of Science, The University of Osaka, Toyonaka, Osaka, Japan.
Masatomo TakahashiDivision of Metabolomics, Medical Research Center for High Depth Omics, Medical Institute of Bioregulation, Kyushu University, Fukuoka, Fukuoka, Japan.ORCID http://orcid.org/0000-0002-2493-2684
Kosuke HataDivision of Metabolomics, Medical Research Center for High Depth Omics, Medical Institute of Bioregulation, Kyushu University, Fukuoka, Fukuoka, Japan.ORCID http://orcid.org/0000-0002-2278-4796
Yoshihiro IzumiDivision of Metabolomics, Medical Research Center for High Depth Omics, Medical Institute of Bioregulation, Kyushu University, Fukuoka, Fukuoka, Japan.ORCID http://orcid.org/0000-0003-4608-4652
Takeshi BambaDivision of Metabolomics, Medical Research Center for High Depth Omics, Medical Institute of Bioregulation, Kyushu University, Fukuoka, Fukuoka, Japan.ORCID http://orcid.org/0000-0002-7442-2738
Koichi FukaseDepartment of Chemistry, Graduate School of Science, The University of Osaka, Toyonaka, Osaka, Japan.ORCID http://orcid.org/0000-0001-8844-0710
Michisato ToyodaDepartment of Physics, Graduate School of Science, The University of Osaka, Toyonaka, Osaka, Japan.ORCID http://orcid.org/0000-0001-5950-6039

Funding

Japan Agency for Medical Research and Development (AMED) JP23ama121055MEXT | Japan Society for the Promotion of Science (JSPS) JP23K17880MEXT | JST | Precursory Research for Embryonic Science and Technology (PRESTO) JPMJPR20E4
6 · The paper itself

Abstract

The development of analytical technology that allows investigation of the diversity of cells that form biological tissues based on molecular information is important to elucidate the heterogeneity of cells and pathological mechanisms. Here, we present a proof-of-concept demonstration of single-cell mass spectrometry imaging (SC-MSI) via tapping-mode scanning probe electrospray ionization (t-SPESI), which is an atmospheric-pressure sampling ionization technique. We developed a novel t-SPESI unit that can be used in combination with an inverted fluorescence microscope and basic technologies to extract components from microregions of cells and measure ions with high sensitivity. We performed multimodal (fluorescence, lipid ion, and topographic) imaging of two types of HeLa cells labeled with fluorescent dyes and chemically fixed and showed the potential for subcellular-scale analysis of both cell structure and chemical composition. Furthermore, we evaluated the lipid species by comparing the SC-MSI results with those of supercritical fluid chromatography tandem mass spectrometry. The technical advancement presented here is effective for distinguishing cell types based on the signal intensity of lipid ions in single cells and investigating differences in the subcellular localization of lipids in different types of cells.

Identifiers

PMID40369247
PMCPMC12078573

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.