Summary of Study ST002190

This data is available at the NIH Common Fund's National Metabolomics Data Repository (NMDR) website, the Metabolomics Workbench, https://www.metabolomicsworkbench.org, where it has been assigned Project ID PR001396. The data can be accessed directly via it's Project DOI: 10.21228/M88H8K This work is supported by NIH grant, U2C- DK119886.

See: https://www.metabolomicsworkbench.org/about/howtocite.php

This study contains a large results data set and is not available in the mwTab file. It is only available for download via FTP as data file(s) here.

Show all samples  
Download mwTab file (text)   |  Download mwTab file(JSON)   |  Download data files (Contains raw data)
Study IDST002190
Study TitleMass Spectrometry Imaging of Lipids In A Gut Epithelial Cell Model
Study TypeMass spectromery imaging of cells.
Study SummaryScope: The Caco2/HT29-MTX co-culture system is widely used as a cell model of the intestinal epithelium. Although the gut epithelium plays an important role in the uptake of free fatty acids and the resynthesis of triglycerides the lipid distribution profile of the co-culture system is not well understood. Desorption electrospray ionization (DESI) is a mass spectrometry (MS) technique which has been widely used to study the main classes of lipid molecules on different tissue surfaces. This has been used to map lipid species and their distribution in Caco2 and HT29-MTX co-culture system. Methods and results: Caco2 and HT29-MTX cells were seeded on coverslips either singly or as cocultures in ratios of 75:25 and 50:50. Cells were cultured for 21 days before MS imaging using a DESI source in both the positive and negative ionization modes. The identity of selected lipids was confirmed in negative and positive ionisation modes using tandem MS. Although many lipids were common to both cell lines, there were distinctive patterns in the lipidomes. Thus, the lipidome of Caco2 cells was more heterogeneous and rich in cholesterol esters and triglycerides whilst HT29-MTX cells has a distinctive lipidome relating to phosphatidylethanolamines, phosphatidylinositols and odd chain lipids, including C17 fatty acids. Conclusion: DESI-MSI has shown that Caco2 and HT29-MTX cells have distinctive lipidomes which are still evident when the cells are cocultured. It has potential to both allow further validation of these widely used cell models and provide insights into how dietary components may modify lipid metabolism in future.
Institute
Manchester Institute of Biotechnology, University of Manchester
Last NameMattar
First NameHadeer
AddressManchester Institute of Biotechnology, Princess Street, Manchester, UK, M1 7DN
Emailhmatar@bu.edu.sa
Phone0161 306 6000
Submit Date2022-05-11
Raw Data AvailableYes
Raw Data File Type(s)mzML
Analysis Type DetailMS(Dir. Inf.)
Release Date2022-07-06
Release Version1
Hadeer Mattar Hadeer Mattar
https://dx.doi.org/10.21228/M88H8K
ftp://www.metabolomicsworkbench.org/Studies/ application/zip

Select appropriate tab below to view additional metadata details:


Project:

Project ID:PR001396
Project DOI:doi: 10.21228/M88H8K
Project Title:Mass Spectrometry Imaging of Lipids In A Gut Epithelial Cell Model
Project Type:MS imaging of cells
Project Summary:Mass spectrometry imaging of lipids in a gut epithelial cell model
Institute:University of Manchester
Last Name:Mattar
First Name:Hadeer
Address:Manchester Institute of Biotechnology, Princess Street, Manchester, UK, M1 7DN
Email:hmatar@bu.edu.sa
Phone:0161 306 6000
  logo