- Confirmed: 这个参考离子已经通过手动审计得到确认和验证。
- Reliable: 这个参考离子可能在特定的解剖组织环境中高度保守。
- Unreliable: 这个参考离子具有较高的排名价值,但缺乏可重复性。
- Unavailable: 由于排名价值低且缺乏可重复性,这个参考离子不应用于注释。
Found 5 Reference Ions Near m/z 231.1133
NovoCell ID | m/z | Mass Window | Metabolite | Ranking | Anatomy Context |
---|---|---|---|---|---|
MSI_000046019 Reliable | 231.1205 | 231.1205 ~ 231.1205 MzDiff: none |
Dienestrol (BioDeep_00000006659) Formula: C18H18O2 (266.1307) |
7.06 (100%) | Mus musculus [UBERON:0002107] liver |
MSI_000054398 Reliable | 231.1178 | 231.1171 ~ 231.118 MzDiff: 3.6 ppm |
Dienestrol (BioDeep_00000006659) Formula: C18H18O2 (266.1307) |
2.56 (100%) | MALDI - CHCA [NOVOCELL:BACKGROUND] blank |
MSI_000033352 Unreliable | 231.1178 | 231.1178 ~ 231.1178 MzDiff: none |
Dienestrol (BioDeep_00000006659) Formula: C18H18O2 (266.1307) |
2.19 (100%) | Posidonia oceanica [PO:0005352] xylem |
MSI_000037456 Unreliable | 231.1185 | 231.1185 ~ 231.1185 MzDiff: none |
Dienestrol (BioDeep_00000006659) Formula: C18H18O2 (266.1307) |
1.71 (100%) | Posidonia oceanica [UBERON:0000329] hair root |
MSI_000056983 Unreliable | 231.1133 | 231.1133 ~ 231.1133 MzDiff: none |
Dienestrol (BioDeep_00000006659) Formula: C18H18O2 (266.1307) |
1.51 (100%) | Homo sapiens [UBERON:0007779] transudate |
Found 5 Sample Hits
Metabolite | Species | Sample | |
---|---|---|---|
Dienestrol Formula: C18H18O2 (266.1307) Adducts: [M+H-2H2O]+ (Ppm: 1.2) |
Posidonia oceanica (root) |
20190613_MS1_A19r-18Resolution: 17μm, 246x264
|
|
Dienestrol Formula: C18H18O2 (266.1307) Adducts: [M+H-2H2O]+ (Ppm: 7.3) |
Posidonia oceanica (root) |
20190828_MS1_A19r-22Resolution: 17μm, 292x279
|
|
Dienestrol Formula: C18H18O2 (266.1307) Adducts: [M+H-2H2O]+ (Ppm: 5.1) |
Posidonia oceanica (root) |
MS1_20180404_PO_1200Resolution: 17μm, 193x208
|
|
Dienestrol Formula: C18H18O2 (266.1307) Adducts: [M+H-2H2O]+ (Ppm: 15.2) |
Homo sapiens (esophagus) |
LNTO22_1_4Resolution: 17μm, 82x80
|
|
Dienestrol Formula: C18H18O2 (266.1307) Adducts: [M+H-2H2O]+ (Ppm: 15.9) |
Mus musculus (Liver) |
Salmonella_final_pos_recalResolution: 17μm, 691x430
A more complete and holistic view on host–microbe interactions is needed to understand the physiological and cellular barriers that affect the efficacy of drug treatments and allow the discovery and development of new therapeutics. Here, we developed a multimodal imaging approach combining histopathology with mass spectrometry imaging (MSI) and same section imaging mass cytometry (IMC) to study the effects of Salmonella Typhimurium infection in the liver of a mouse model using the S. Typhimurium strains SL3261 and SL1344. This approach enables correlation of tissue morphology and specific cell phenotypes with molecular images of tissue metabolism. IMC revealed a marked increase in immune cell markers and localization in immune aggregates in infected tissues. A correlative computational method (network analysis) was deployed to find metabolic features associated with infection and revealed metabolic clusters of acetyl carnitines, as well as phosphatidylcholine and phosphatidylethanolamine plasmalogen species, which could be associated with pro-inflammatory immune cell types. By developing an IMC marker for the detection of Salmonella LPS, we were further able to identify and characterize those cell types which contained S. Typhimurium.
[dataset] Nicole Strittmatter. Holistic Characterization of a Salmonella Typhimurium Infection Model Using Integrated Molecular Imaging, metabolights_dataset, V1; 2022. https://www.ebi.ac.uk/metabolights/MTBLS2671. |
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