Summary of Study ST001475
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.
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.
| Study ID | ST001475 |
| Study Title | Metabolomics of lung injury after allogeneic hematopoietic cell transplantation - Liver DI-FTMS |
| Study Type | preliminary data |
| Study Summary | Allogeneic 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 |
| Department | MCC |
| Last Name | Hildebrandt |
| First Name | Gerhard |
| Address | CTW-453, 900 South Limestone street. UKY. Lexington, Kentucky-40536 |
| gerhard.hildebrandt@uky.edu | |
| Phone | 800-333-8874 |
| Submit Date | 2020-08-21 |
| Raw Data Available | Yes |
| Raw Data File Type(s) | raw(Thermo) |
| Analysis Type Detail | MS(Dir. Inf.) |
| Release Date | 2020-09-10 |
| Release Version | 1 |
Select appropriate tab below to view additional metadata details:
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: | SU001549 |
| 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 |
|---|---|---|
| SA124583 | 07_C1-1_Liver_allogenic_42days_170427_UKy_GCH_rep1-lipid | allogenic |
| SA124584 | 13_C1-1_Liver_allogenic_7days_170427_UKy_GCH_rep1-lipid | allogenic |
| SA124585 | 15_C1-20_Liver_allogenic_7days_170427_UKy_GCH_rep3-lipid | allogenic |
| SA124586 | 09_C2-0_Liver_allogenic_42days_170427_UKy_GCH_rep1-lipid | allogenic |
| SA124587 | 08_C1-2_Liver_allogenic_42days_170427_UKy_GCH_rep2-lipid | allogenic |
| SA124588 | 14_C1-2_Liver_allogenic_7days_170427_UKy_GCH_rep2-lipid | allogenic |
| SA124589 | 03_A2_Liver_naive_0days_170427_UKy_GCH_rep3-lipid | naive |
| SA124590 | 02_A1_Liver_naive_0days_170427_UKy_GCH_rep2-lipid | naive |
| SA124591 | 01_A0_Liver_naive_0days_170427_UKy_GCH_rep1-lipid | naive |
| SA124592 | 05_B1_Liver_syngenic_42days_170427_UKy_GCH_rep2-lipid | syngenic |
| SA124593 | 10_B1-0_Liver_syngenic_7days_170427_UKy_GCH_rep1-lipid | syngenic |
| SA124594 | 04_B0_Liver_syngenic_42days_170427_UKy_GCH_rep1-lipid | syngenic |
| SA124595 | 12_B1-2_Liver_syngenic_7days_170427_UKy_GCH_rep3-lipid | syngenic |
| SA124596 | 11_B1-1_Liver_syngenic_7days_170427_UKy_GCH_rep2-lipid | syngenic |
| SA124597 | 06_B2_Liver_syngenic_42days_170427_UKy_GCH_rep3-lipid | syngenic |
| Showing results 1 to 15 of 15 |
Collection:
| Collection ID: | CO001544 |
| Collection Summary: | Mouse is sacrificed and tissues are harvested. |
| Collection Protocol ID: | mouse_tissue_collection |
| Sample Type: | Multiple tissues |
Treatment:
| Treatment ID: | TR001564 |
| 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: | SP001557 |
| Sampleprep Summary: | Protein extraction and quantification. Lipid extraction from homogenate. Tissue is frozen in liquid nitrogen to stop metabolic processes. Frozen tissue is ground in a SPEX grinder under liquid nitrogen to homogenize the sample. |
| Sampleprep Protocol ID: | tissue_quench; frozen_tissue_grind; lipid_extraction; protein_extraction |
| Sampleprep Protocol Filename: | 4B_Extract_Polar_Lipid_Prot_Fan_070417.pdf 4D_17Jun4_Fan_Prot_Quant.pdf |
Combined analysis:
| Analysis ID | AN002451 |
|---|---|
| Analysis type | MS |
| Chromatography type | None (Direct infusion) |
| Chromatography system | None |
| Column | None |
| MS Type | ESI |
| MS instrument type | Orbitrap |
| MS instrument name | Thermo Q Exactive Orbitrap |
| Ion Mode | POSITIVE |
| Units | peak_height |
Chromatography:
| Chromatography ID: | CH001796 |
| Chromatography Summary: | None |
| Instrument Name: | None |
| Column Name: | None |
| Chromatography Type: | None (Direct infusion) |
MS:
| MS ID: | MS002274 |
| Analysis ID: | AN002451 |
| Instrument Name: | Thermo Q Exactive Orbitrap |
| Instrument Type: | Orbitrap |
| MS Type: | ESI |
| MS Comments: | Xcalibur software. LipidSearch for data processing. |
| Ion Mode: | POSITIVE |
