Summary of Study ST001463

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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Study IDST001463
Study TitleMetabolomics of lung injury after allogeneic hematopoietic cell transplantation - Small Intenstines NMR 1D
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)fid
Analysis Type DetailNMR
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:SU001537
Subject Type:Mammal
Subject Species:Mus musculus
Taxonomy ID:10090
Species Group:Mammals

Factors:

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

mb_sample_id local_sample_id Treatment Protocol
SA12426815_C1-20_SI_allogenic_7days_170427_UKy_GCH_rep3-polar-NMR_Aallogenic
SA12426909_C2-0_SI_allogenic_42days_170427_UKy_GCH_rep1-polar-NMR_Aallogenic
SA12427007_C1-1_SI_allogenic_42days_170427_UKy_GCH_rep1-polar-NMR_Aallogenic
SA12427113_C1-1_SI_allogenic_7days_170427_UKy_GCH_rep1-polar-NMR_Aallogenic
SA12427208_C1-2_SI_allogenic_42days_170427_UKy_GCH_rep2-polar-NMR_Aallogenic
SA12427314_C1-2_SI_allogenic_7days_170427_UKy_GCH_rep2-polar-NMR_Aallogenic
SA12427401_A0_SI_naive_0days_170427_UKy_GCH_rep1-polar-NMR_Anaive
SA12427503_A2_SI_naive_0days_170427_UKy_GCH_rep3-polar-NMR_Anaive
SA12427602_A1_SI_naive_0days_170427_UKy_GCH_rep2-polar-NMR_Anaive
SA12427705_B1_SI_syngenic_42days_170427_UKy_GCH_rep2-polar-NMR_Asyngenic
SA12427812_B1-2_SI_syngenic_7days_170427_UKy_GCH_rep3-polar-NMR_Asyngenic
SA12427910_B1-0_SI_syngenic_7days_170427_UKy_GCH_rep1-polar-NMR_Asyngenic
SA12428011_B1-1_SI_syngenic_7days_170427_UKy_GCH_rep2-polar-NMR_Asyngenic
SA12428104_B0_SI_syngenic_42days_170427_UKy_GCH_rep1-polar-NMR_Asyngenic
SA12428206_B2_SI_syngenic_42days_170427_UKy_GCH_rep3-polar-NMR_Asyngenic
Showing results 1 to 15 of 15

Collection:

Collection ID:CO001532
Collection Summary:Mouse is sacrificed and tissues are harvested.
Collection Protocol ID:mouse_tissue_collection
Sample Type:Multiple tissues

Treatment:

Treatment ID:TR001552
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:SP001545
Sampleprep Summary:Polar extraction from homogenate, lypholized, and frozen. Frozen tissue is ground in a SPEX grinder under liquid nitrogen to homogenize the sample. Protein extraction and quantification. Tissue is frozen in liquid nitrogen to stop metabolic processes.
Sampleprep Protocol ID:polar_extraction; protein_extraction; frozen_tissue_grind; tissue_quench
Sampleprep Protocol Filename:4D_17Jun4_Fan_Prot_Quant.pdf
4B_Extract_Polar_Lipid_Prot_Fan_070417.pdf

Analysis:

Analysis ID:AN002438
Analysis Type:NMR
Num Factors:3
Num Metabolites:257
Units:normalized peak area

NMR:

NMR ID:NM000177
Analysis ID:AN002438
Instrument Name:Agilent 600
Instrument Type:FT-NMR
NMR Experiment Type:PRESAT (1H1D)
Standard Concentration:0.5 mM
Spectrometer Frequency:600 MHz
NMR Probe:cryogenic triple resonance HCN
NMR Solvent:D20
NMR Tube Size:1.7 mm
Shimming Method:gradient shimming
Pulse Sequence:PRESAT
Water Suppression:presaturation
Chemical Shift Ref Cpd:DSS
Temperature:15 celsius
Acquisition Time:2 s
Relaxation Delay:4 s
Baseline Correction Method:Bernstein Polynomial
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