Summary of Study ST001206
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 PR000811. The data can be accessed directly via it's Project DOI: 10.21228/M8VD62 This work is supported by NIH grant, U2C- DK119886.
See: https://www.metabolomicsworkbench.org/about/howtocite.php
Study ID | ST001206 |
Study Title | Effects of cold exposure on serum lipidomic in mice |
Study Summary | We aimed to identify lipids released during cold exposure from adipose tissue, with a role in adaptive thermogenesis. |
Institute | Joslin Diabetes Center |
Department | Integrative Physiology and Metabolism |
Laboratory | Yu-Hua Tseng lab |
Last Name | Leiria |
First Name | Luiz |
Address | One Joslin Place, Boston-MA, USA, 02215 |
luiz.leiria@joslin.harvard.edu | |
Phone | 1 6173091967 |
Submit Date | 2019-06-26 |
Study Comments | Joslin Diabetes Center affiliate of Harvard Medical School |
Raw Data Available | Yes |
Raw Data File Type(s) | wiff |
Analysis Type Detail | LC-MS |
Release Date | 2019-07-17 |
Release Version | 1 |
Select appropriate tab below to view additional metadata details:
Project:
Project ID: | PR000811 |
Project DOI: | doi: 10.21228/M8VD62 |
Project Title: | 12-LOX metabolites in cold adaptation |
Project Summary: | The goal of this project is to understand the role of the enzyme 12-lipoxygenase in the adaptive thermogenesis. We found this enzyme is activated by cold stimulation, then producing lipid metabolites in adipose tissue and releasing them into the circulation to regulate fuel utilisation and thermogenic pathways required for the cold adaptation. |
Institute: | Joslin Diabetes Center |
Department: | Integrative Physiology and Metabolism |
Laboratory: | Yu-Hua Tseng lab |
Last Name: | Leiria |
First Name: | Luiz |
Address: | One Joslin Place, Boston, MA-USA, 02215 |
Email: | luiz.leiri@joslin.harvard.edu |
Phone: | 1 6173091967 |
Subject:
Subject ID: | SU001273 |
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 | Temperature | Time of exposure |
---|---|---|---|
SA084770 | Control 1 | 22C | 1 hour |
SA084771 | Control 2 | 22C | 1 hour |
SA084772 | Control 5 | 22C | 1 hour |
SA084773 | Control 6 | 22C | 1 hour |
SA084774 | Control 4 | 22C | 1 hour |
SA084775 | Control 3 | 22C | 1 hour |
SA084776 | Thermoneutral 2 female | 30C | 7 days |
SA084777 | Thermoneutral 1 female | 30C | 7 days |
SA084778 | Thermoneutral 3 female | 30C | 7 days |
SA084779 | Thermoneutral 6 female | 30C | 7 days |
SA084780 | Thermoneutral 5 male | 30C | 7 days |
SA084781 | Thermoneutral 5 female | 30C | 7 days |
SA084782 | Thermoneutral 4 female | 30C | 7 days |
SA084783 | Thermoneutral 6 male | 30C | 7 days |
SA084784 | Thermoneutral 4 male | 30C | 7 days |
SA084785 | Thermoneutral 1 male | 30C | 7 days |
SA084786 | Thermoneutral 2 male | 30C | 7 days |
SA084787 | Thermoneutral 3 male | 30C | 7 days |
SA084788 | 1-hr cold 1 | 5C | 1 hour |
SA084789 | 1-hr cold 2 | 5C | 1 hour |
SA084790 | 1-hr cold 3 | 5C | 1 hour |
SA084791 | 1-hr cold 4 | 5C | 1 hour |
SA084792 | 1-hr cold 5 | 5C | 1 hour |
SA084793 | Cold 3 female | 5C | 7 days |
SA084794 | Cold 4 female | 5C | 7 days |
SA084795 | Cold 5 female | 5C | 7 days |
SA084796 | Cold 2 female | 5C | 7 days |
SA084797 | Cold 2 male | 5C | 7 days |
SA084798 | Cold 1 male | 5C | 7 days |
SA084799 | Cold 3 male | 5C | 7 days |
SA084800 | Cold 4 male | 5C | 7 days |
SA084801 | Cold 5 male | 5C | 7 days |
SA084802 | Cold 1 female | 5C | 7 days |
Showing results 1 to 33 of 33 |
Collection:
Collection ID: | CO001267 |
Collection Summary: | Mice were anaesthethized with isoflurane, the blood collected through cardiac puncture, and left under room temperature for 30 minutes. After that, the blood was centrifuged for 3 minutes at 14,000 rpm. Then, serum was transferred for a clean 1.5ml microbe and frost. |
Sample Type: | Blood (serum) |
Storage Conditions: | -20℃ |
Treatment:
Treatment ID: | TR001288 |
Treatment Summary: | We divided the C57BL6/J mice in 6 groups: females housed in 30C degree for 1 week and females housed in 5C degree for 1 week; Males housed in 30C degree for 1 week and females housed in 5C degree for 1 week; males housed in 22C for 1 hour and males housed in 5C for 1 hour. |
Sample Preparation:
Sampleprep ID: | SP001281 |
Sampleprep Summary: | Aliquots of 100 µL serum or were taken. A mixture of deuterium-labeled internal standards was added to each aliquot, followed by 3x volume of sample of cold methanol (MeOH). Samples were vortexed for 5 minutes and stored at −20 °C overnight. Cold samples were centrifuged at 14,000g for 10 minutes, and the supernatant was then transferred to a new tube and 3 mL of acidified H2O (pH 3.5) was added to each sample prior to C18 SPE. The methyl formate fractions were collected, dried under nitrogen, and reconstituted in 50 µL MeOH:H2O (1:1, by vol). Samples were transferred to 0.5 mL tubes and centrifuged at 20,000g at 4 °C for 10 minutes. (35ul) of supernatant was transferred to LC–MS/MS vials for analysis using the BERG LC–MS/MS mediator lipidomics platform. |
Combined analysis:
Analysis ID | AN002008 |
---|---|
Analysis type | MS |
Chromatography type | Reversed phase |
Chromatography system | Ekspert MicroLC 200 system |
Column | Phenomenex Synergi Fusion-RP capillary C18 (150 × 0.5 mm,4um) |
MS Type | ESI |
MS instrument type | Triple TOF |
MS instrument name | ABI Sciex 5600+ TripleTOF |
Ion Mode | NEGATIVE |
Units | Peak Area |
Chromatography:
Chromatography ID: | CH001452 |
Instrument Name: | Ekspert MicroLC 200 system |
Column Name: | Phenomenex Synergi Fusion-RP capillary C18 (150 × 0.5 mm,4um) |
Chromatography Type: | Reversed phase |
MS:
MS ID: | MS001861 |
Analysis ID: | AN002008 |
Instrument Name: | ABI Sciex 5600+ TripleTOF |
Instrument Type: | Triple TOF |
MS Type: | ESI |
MS Comments: | MS spectra were acquired in high-resolution mode (>30,000) using a 100-ms accumulation time per spectrum. Full-scan MS/MS was acquired in high sensitivity mode, with an accumulation time optimized per cycle. Collision energy was set using rolling collision energy with a spread of 15V. The identity of a component was confirmed using PeakView® software (SCIEX), and quantification was performed using MultiQuant™ software (SCIEX). |
Ion Mode: | NEGATIVE |