Summary of Study ST004302

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 PR002718. The data can be accessed directly via it's Project DOI: 10.21228/M8B26Z 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 IDST004302
Study TitleMetabolomic analysis of wild-type and TauT-/- murine Mesenchymal Stromal Cells (MSCs)
Study Summary16 week old TauT+/+ and TauT-/- mice were sacrificed, stromal populations were isolated and magnetically enriched or flow sorted for MSCs (CD45-Ter119-). MSC cultures were washed with PBS and detached using TrypLE. Cells were washed with PBS containing 5 mM glucose and centrifuged at 3000g for 1 min, snap frozen, and processed for untargeted metabolomics.
Institute
University of Rochester Medical Center
Last NameSmith
First NameBradley
Address575 Elmwood Ave, Rochester, NY, 14620
Emailbradley_smith@urmc.rochester.edu
Phone585-275-1445
Submit Date2025-10-17
Raw Data AvailableYes
Raw Data File Type(s)mzML
Analysis Type DetailLC-MS
Release Date2025-11-12
Release Version1
Bradley Smith Bradley Smith
https://dx.doi.org/10.21228/M8B26Z
ftp://www.metabolomicsworkbench.org/Studies/ application/zip

Select appropriate tab below to view additional metadata details:


Project:

Project ID:PR002718
Project DOI:doi: 10.21228/M8B26Z
Project Title:Metabolomic analysis of wild-type and TauT-/- murine Mesenchymal Stromal Cells (MSCs)
Project Summary:Bone marrow mesenchymal stromal cells (BMSCs) are a type of multipotent stem cell found in the bone marrow stroma that can differentiate into various cell types, support the bone marrow's microenvironment, and regulate other stem cells. Their key functions include providing physical support to hematopoietic stem cells, secreting factors that control their homeostasis, and undergoing differentiation into bone, cartilage, and fat cells. BMSCs are also being explored for various cell therapies due to their ability to be expanded in vitro. To determine the role of taurine in regulating metabolism of bone marrow mesenchymal stromal cells (MSCs), we carried out untargeted metabolomic analysis of murine taurine transporter (TauT) wild-type and knockout MSCs. Briefly, 16 week old TauT+/+ and TauT-/- mice were sacrificed, stromal populations were isolated and magnetically enriched or flow sorted for MSCs. Next, untargeted metabolomic analysis was carried out to identify metabolic changes induced by inhibiting taurine uptake in MSCs. This analysis identified inositol metabolism as a downstream effector of taurine in MSCs.
Institute:University of Rochester Medical Center
Last Name:Smith
First Name:Bradley
Address:575 Elmwood Ave, Rochester, NY, 14620
Email:bradley_smith@urmc.rochester.edu
Phone:585-275-1445

Subject:

Subject ID:SU004455
Subject Type:Mammal
Subject Species:Mus musculus
Taxonomy ID:10090

Factors:

Subject type: Mammal; Subject species: Mus musculus (Factor headings shown in green)

mb_sample_id local_sample_id Sample source Genotype
SA505185KO_1a_7Mesenchymal Stromal Cells KO
SA505186KO_1b_8Mesenchymal Stromal Cells KO
SA505187KO_2a_3Mesenchymal Stromal Cells KO
SA505188KO_2b_4Mesenchymal Stromal Cells KO
SA505189KO_6a_10Mesenchymal Stromal Cells KO
SA505190WT_1a_1Mesenchymal Stromal Cells WT
SA505191WT_1b_2Mesenchymal Stromal Cells WT
SA505192WT_2a_5Mesenchymal Stromal Cells WT
SA505193WT_2b_6Mesenchymal Stromal Cells WT
SA505194WT_6a_9Mesenchymal Stromal Cells WT
Showing results 1 to 10 of 10

Collection:

Collection ID:CO004448
Collection Summary:16 week old TauT+/+ and TauT-/- mice were sacrificed, stromal populations were isolated and magnetically enriched or flow sorted for MSCs (CD45-Ter119-). MSC cultures were washed with PBS and detached using TrypLE. Cells were washed with PBS containing 5mM glucose and centrifuged at 3000g for 1 min, snap frozen, and processed for untargeted metabolomics.
Sample Type:Mesenchymal stromal cells

Treatment:

Treatment ID:TR004464
Treatment Summary:N/A

Sample Preparation:

Sampleprep ID:SP004461
Sampleprep Summary:Frozen cell pellets were resuspended at 1 million cells per 1 mL of 80% MeOH via vortexing, transferred to -80°C for 30 min and then regular ice for 30 minutes with vortexing every 10 minutes. Next, samples were centrifuged at 17,000x g for 10 minutes and 90% of supernatant was dried down in a vacuum evaporator (Thermo). Samples were reconstituted in 50% acetonitrile (A955, Fisher Scientific), at a volume equal to 10% of dried down volume, and transferred to glass vials for LC/MS analysis.

Chromatography:

Chromatography ID:CH005437
Instrument Name:Thermo Vanquish
Column Name:Waters XBridge XP BEH Amide (150 mm x 2.1 mm, 2.5 µm)
Column Temperature:25℃
Flow Gradient:0 minutes, 100% B; 2 minutes, 100% B; 3 minutes, 90% B; 5 minutes, 90% B; 6 minutes, 85% B; 7 minutes, 85% B; 8 minutes, 75% B; 9 minutes, 75% B; 10 minutes, 55% B; 12 minutes, 55% B; 13 minutes, 35%, 20 minutes, 35% B; 20.1 minutes, 35% B; 20.6 minutes, 100% B; 22.2 minutes, 100% B; 28 minutes, 100% B.
Flow Rate:150 μL/min for first 22.7 minutes, then 300 μL/min for 22.7 to 28 minutes
Solvent A:100% water; 10 mM ammonium acetate; 0.1% ammonium hydroxide; 0.1% medronic acid
Solvent B:90% acetonitrile/10% water; 10 mM ammonium acetate; 0.1% ammonium hydroxide; 0.1% medronic acid
Chromatography Type:HILIC
  
Chromatography ID:CH005438
Instrument Name:Thermo Vanquish
Column Name:Waters XBridge XP BEH Amide (150 mm x 2.1 mm, 2.5 µm)
Column Temperature:25℃
Flow Gradient:0 minutes, 100% B; 2 minutes, 100% B; 3 minutes, 90% B; 5 minutes, 90% B; 6 minutes, 85% B; 7 minutes, 85% B; 8 minutes, 75% B; 9 minutes, 75% B; 10 minutes, 55% B; 12 minutes, 55% B; 13 minutes, 35%, 20 minutes, 35% B; 20.1 minutes, 35% B; 20.6 minutes, 100% B; 22.2 minutes, 100% B; 28 minutes, 100% B.
Flow Rate:150 μL/min for first 22.7 minutes, then 300 μL/min for 22.7 to 28 minutes
Solvent A:100% water; 10 mM ammonium formate; 0.125% formic acid
Solvent B:90% acetonitrile/10% water; 10 mM ammonium formate; 0.125% formic acid
Chromatography Type:HILIC

Analysis:

Analysis ID:AN007158
Analysis Type:MS
Chromatography ID:CH005437
Has Mz:1
Has Rt:1
Rt Units:Minutes
Results File:ST004302_AN007158_Results.txt
Units:area
  
Analysis ID:AN007159
Analysis Type:MS
Chromatography ID:CH005438
Has Mz:1
Has Rt:1
Rt Units:Minutes
Results File:ST004302_AN007159_Results.txt
Units:area
  logo