Summary of Study ST002469

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 PR001595. The data can be accessed directly via it's Project DOI: 10.21228/M8J13B 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  |  Perform analysis on untargeted data  
Download mwTab file (text)   |  Download mwTab file(JSON)   |  Download data files (Contains raw data)
Study IDST002469
Study TitleMesenchymal stromal cell (MSC) Metabolite MS study
Study TypeUntargeted Metabolite Study
Study SummaryMetabolomics and lipidomics workflows were used to analyze Mesenchymal stromal cell (MSC) metabolites. Metabolite abundances were used to model MSC potency results in IDO and T-cell proliferation assays.
Institute
Georgia Institute of Technology
DepartmentChemistry and Biochemistry
LaboratoryFernandez Lab
Last NameVan Grouw
First NameAlexandria
Address311 Ferst Dr. NW Atlanta, GA 30332
Emailagrouw3@gatech.edu
Phone7072391412
Submit Date2023-02-07
Raw Data AvailableYes
Raw Data File Type(s)raw(Thermo)
Analysis Type DetailLC-MS
Release Date2023-02-26
Release Version1
Alexandria Van Grouw Alexandria Van Grouw
https://dx.doi.org/10.21228/M8J13B
ftp://www.metabolomicsworkbench.org/Studies/ application/zip

Select appropriate tab below to view additional metadata details:


Project:

Project ID:PR001595
Project DOI:doi: 10.21228/M8J13B
Project Title:Development of a Robust Consensus Modeling Approach for Identifying Cellular and Media Metabolites Predictive of Mesenchymal Stromal Cell Potency
Project Type:MS Untargeted Analysis
Project Summary:Mesenchymal stromal cells (MSCs) have shown promise in regenerative medicine applications due in part to their ability to modulate immune cells, such as T cells. However, MSCs demonstrate significant functional heterogeneity in terms of their immunomodulatory function because of differences in MSC donor/tissue source, as well as non-standardized manufacturing approaches. As MSC metabolism plays a critical role in their ability to expand to therapeutic numbers ex vivo, we comprehensively profiled intracellular and extracellular metabolites throughout the expansion process to identify predictors of MSC immunomodulatory function (T cell modulation and indoleamine-2,3-dehydrogenase (IDO) activity). Here, we profiled media metabolites in a non-destructive manner through daily sampling and nuclear magnetic resonance (NMR), as well as MSC intracellular metabolites at the end of expansion using mass spectrometry (MS). Using a robust consensus machine learning approach, we were able to identify panels of metabolites predictive of MSC immunomodulatory function for 10 independent MSC lines.
Institute:Georgia Institute of Technology
Department:Chemistry and Biochemistry
Laboratory:Fernandez Lab
Last Name:Van Grouw
First Name:Alexandria
Address:311 Ferst Dr. NW Atlanta, GA 30332
Email:agrouw3@gatech.edu
Phone:7072391412
Funding Source:NSF Center for Cell Manufacturing Technologies
  logo