Summary of Study ST001470

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 PR000993. The data can be accessed directly via it's Project DOI: 10.21228/M8BH7T This work is supported by NIH grant, U2C- DK119886.

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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.

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Study IDST001470
Study TitleMetabolomics of lung injury after allogeneic hematopoietic cell transplantation - Lung ICMS
Study Typepreliminary data
Study SummaryAllogeneic hematopoietic cell transplantation (allo-HCT) is a potentially curative treatment option for a variety of hematological malignancies. Interactions between the donor immune system and the patient tissue result in a disease, called GVHD. The pathophysiology of acute GVHD can be hypothesized in three sequential phases: cytokine storm and activation of the antigen-presenting cells (APC), donor T cell activation and effector cell phase. Idiopathic pneumonia syndrome (IPS) is one of the most deleterious complications after allogeneic HCT and is considered not only to be related to conditioning regimen toxicity but also represents an end organ damage caused by allo-reactive T cells, therefore making the lung susceptible to a two-pronged attack, one of which overlaps with GVHD causing other target organ injury. IPS results in mortality of up to 90% of patients. We will use a murine model of IPS and GVHD which is well established in our group, and in which disease evolves either across disparities in major histocompatibility complex (MCH) class I and II, minor histocompatibility antigens (miHags) or both. Metabolomics changes following syngeneic and allogeneic HCT at post-transplantation Days +7 (cytokine storm phase) and Days +42 (cellular effector phase) are compared to baseline wild-type (naive) controls. Prior to analysis, naïve - and experimental mice (N=3 from each group) were fed with semi-liquid diet supplemented with tracers (13C6-glucose ) over 24 hours. At the end of 7 days or 42 days, respectively, feces and aGVHD target organs (colon, liver and lung) were collected from all groups and further processed and / or analyzed. We expect to reveal metabolic pathways affected after allo-HCT which contribute to immune cell mediated lung injury (IPS) and will potentially identify different metabolic pathways in other GVHD target organs.
Institute
University of Kentucky
DepartmentMCC
Last NameHildebrandt
First NameGerhard
AddressCTW-453, 900 South Limestone street. UKY. Lexington, Kentucky-40536
Emailgerhard.hildebrandt@uky.edu
Phone800-333-8874
Submit Date2020-08-22
Raw Data AvailableYes
Raw Data File Type(s)raw(Thermo)
Analysis Type DetailLC-MS
Release Date2020-09-10
Release Version1
Gerhard Hildebrandt Gerhard Hildebrandt
https://dx.doi.org/10.21228/M8BH7T
ftp://www.metabolomicsworkbench.org/Studies/ application/zip

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Project:

Project ID:PR000993
Project DOI:doi: 10.21228/M8BH7T
Project Title:Metabolomics of lung injury after allogeneic hematopoietic cell transplantation
Institute:University of Kentucky
Department:Markey Cancer Center
Last Name:Hildebrandt
First Name:Gerhard
Address:Gerhard C. Hildebrandt, MD, Room no. CC401A, Ben Roach Building, Markey Cancer Center University of Kentucky, Lexington, 40536
Email:gerhard.hildebrandt@uky.edu
Phone:800-333-8874

Subject:

Subject ID:SU001544
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 Treatment Protocol
SA12450830_C1-20_Lung_allogenic_7days_170427_UKy_GCH_rep3-polar-ICMS_Aallogenic
SA12450922_C1-1_Lung_allogenic_42days_170427_UKy_GCH_rep1-polar-ICMS_Aallogenic
SA12451024_C2-0_Lung_allogenic_42days_170427_UKy_GCH_rep1-polar-ICMS_Aallogenic
SA12451129_C1-2_Lung_allogenic_7days_170427_UKy_GCH_rep2-polar-ICMS_Aallogenic
SA12451223_C1-2_Lung_allogenic_42days_170427_UKy_GCH_rep2-polar-ICMS_Aallogenic
SA12451328_C1-1_Lung_allogenic_7days_170427_UKy_GCH_rep1-polar-ICMS_Aallogenic
SA12451418_A2_Lung_naive_0days_170427_UKy_GCH_rep3-polar-ICMS_Anaive
SA12451517_A1_Lung_naive_0days_170427_UKy_GCH_rep2-polar-ICMS_Anaive
SA12451616_A0_Lung_naive_0days_170427_UKy_GCH_rep1-polar-ICMS_Anaive
SA12451726_B1-1_Lung_syngenic_7days_170427_UKy_GCH_rep2-polar-ICMS_Asyngenic
SA12451820_B1_Lung_syngenic_42days_170427_UKy_GCH_rep2-polar-ICMS_Asyngenic
SA12451927_B1-2_Lung_syngenic_7days_170427_UKy_GCH_rep3-polar-ICMS_Asyngenic
SA12452021_B2_Lung_syngenic_42days_170427_UKy_GCH_rep3-polar-ICMS_Asyngenic
SA12452119_B0_Lung_syngenic_42days_170427_UKy_GCH_rep1-polar-ICMS_Asyngenic
SA12452225_B1-0_Lung_syngenic_7days_170427_UKy_GCH_rep1-polar-ICMS_Asyngenic
Showing results 1 to 15 of 15

Collection:

Collection ID:CO001539
Collection Summary:Mouse is sacrificed and tissues are harvested.
Collection Protocol ID:mouse_tissue_collection
Sample Type:mouse

Treatment:

Treatment ID:TR001559
Treatment Summary:Mouse with allogenic bone marrow transplant. Fed with semi-liquid diet supplemented with fully labeled glucose for 24 hours before harvest. Mouse with no treatment. Fed with semi-liquid diet supplemented with fully labeled glucose for 24 hours before harvest. Mouse with syngenic bone marrow transplant. Fed with semi-liquid diet supplemented with fully labeled glucose for 24 hours before harvest.
Treatment Protocol ID:allogenic naive syngenic

Sample Preparation:

Sampleprep ID:SP001552
Sampleprep Summary:Protein extraction and quantification. Before going into the IC-FTMS the frozen sample is reconstituted in water. Tissue is frozen in liquid nitrogen to stop metabolic processes. Polar extraction from homogenate, lypholized, and frozen. Frozen tissue is ground in a SPEX grinder under liquid nitrogen to homogenize the sample.
Sampleprep Protocol ID:IC-FTMS_preparation; polar_extraction; tissue_quench; protein_extraction; frozen_tissue_grind
Sampleprep Protocol Filename:4B_Extract_Polar_Lipid_Prot_Fan_070417.pdf
4D_17Jun4_Fan_Prot_Quant.pdf

Combined analysis:

Analysis ID AN002446
Analysis type MS
Chromatography type Ion exchange
Chromatography system Thermo Dionex ICS-5000+
Column Dionex IonPac AS11-HC (250 x 2mm,4um)
MS Type ESI
MS instrument type IC-FTMS
MS instrument name Orbitrap Fusion
Ion Mode NEGATIVE
Units abundance & normalized peak area

Chromatography:

Chromatography ID:CH001791
Chromatography Summary:Targeted IC
Instrument Name:Thermo Dionex ICS-5000+
Column Name:Dionex IonPac AS11-HC (250 x 2mm,4um)
Chromatography Type:Ion exchange

MS:

MS ID:MS002269
Analysis ID:AN002446
Instrument Name:Orbitrap Fusion
Instrument Type:IC-FTMS
MS Type:ESI
MS Comments:ICMS Analytical Experiment with detection of compounds by comparison to standards. Thermo RAW files are loaded into TraceFinder and peaks are manually curated. The area under the chromatograms is then exported to an Excel file. The area is then corrected for natural abundance. The natural abundance corrected area is then used to calculate the concentration of each compound for each sample. This calculation is done using standards. The first sample ran on the ICMS is a standard that has known concentrations of certain compounds. Then a number of samples are ran (typically 3-4) followed by another standard. The equation to calculate the concentration is "intensity in sample"/("intensity in first standard" + (("intensity in second standard" - "intensity in first standard")/# of samples) * "known concentration in standard", where the "intensity" is the aforementioned natural abundance corrected area, and the unlabeled intensity from the standard is used for all isotopologues of the compound. The reconstitution volume is simply the volume that the polar part of the sample was reconstituted to before going into the ICMS. The injection volume is how much of the reconstitution volume was injected into the ICMS. The protein is how much protein was in the entire sample (not only the small portion that was aliquoted for the ICMS). The polar split ratio is the fraction of the polar part of the sample that was aliquoted for the ICMS. This is calculated by dividing the weight of the polar aliquot for ICMS by the total weight of the polar portion of the sample. The protein normalized concentration is calculated using the equation, concentration * (reconstitution volume / 1000 / polar split ratio / protein).
Ion Mode:NEGATIVE
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