Summary of Study ST003359
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 PR002085. The data can be accessed directly via it's Project DOI: 10.21228/M83R6P 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 | ST003359 |
| Study Title | Secretion of phosphatidylcholine from Huh7 cells treated with oleate-d9 or elaidate-d17 |
| Study Summary | We analyzed PC in the fresh and spent media of Huh7 cells treated with BSA-oleate-d9 or BSA-elaidate-d17 to determine their incorporation into secreted phospholipids. We aimed to determine if SM secretory flux in response to fatty acid treatments correlated to PC secretory flux. |
| Institute | Salk Institute for Biological Studies |
| Last Name | Gengatharan |
| First Name | Jivani |
| Address | 10010 N Torrey Pines Rd, La Jolla, CA, 92037, USA |
| jivani14@gmail.com | |
| Phone | (858) 453-4100 |
| Submit Date | 2024-07-30 |
| Raw Data Available | Yes |
| Raw Data File Type(s) | d |
| Analysis Type Detail | LC-MS |
| Release Date | 2024-08-09 |
| Release Version | 1 |
Select appropriate tab below to view additional metadata details:
Project:
| Project ID: | PR002085 |
| Project DOI: | doi: 10.21228/M83R6P |
| Project Title: | Altered sphingolipid biosynthetic flux and lipoprotein trafficking contribute to trans fat-induced atherosclerosis |
| Project Summary: | The goal of the project is to determine the role of sphingolipid metabolism in atherosclerosis induced by dietary trans fat. We analyzed lipid metabolites in Huh7 cells following various fatty acid treatments, with specific focus on cis and trans unsaturated fatty acids. Additionally, we analyzed lipid metabolites in plasma and liver of Ldlr-/- mice fed high-fat diets enriched in cis or trans fatty acids in the presence or absence of myriocin, a pharmacological inhibitor of Serine palmitoyltransferase (SPT), the initial rate-limiting enzyme of sphingolipid biosynthesis. |
| Institute: | Salk Institute for Biological Studies |
| Last Name: | Gengatharan |
| First Name: | Jivani |
| Address: | 10010 N Torrey Pines Rd, La Jolla, CA, 92037, USA |
| Email: | jivani14@gmail.com |
| Phone: | (858) 453-4100 |
Subject:
| Subject ID: | SU003480 |
| Subject Type: | Cultured cells |
| Subject Species: | Homo sapiens |
| Taxonomy ID: | 9606 |
| Cell Strain Details: | Huh7 |
Factors:
Subject type: Cultured cells; Subject species: Homo sapiens (Factor headings shown in green)
| mb_sample_id | local_sample_id | Sample source | Condition |
|---|---|---|---|
| SA365838 | Huh7freshmedia_C30Lip1_elaidicd17_1 | Huh7 media | BSA-elaidate-d17 fresh media |
| SA365839 | Huh7freshmedia_C30Lip1_elaidicd17_2 | Huh7 media | BSA-elaidate-d17 fresh media |
| SA365840 | Huh7freshmedia_C30Lip1_elaidicd17_3 | Huh7 media | BSA-elaidate-d17 fresh media |
| SA365841 | Huh7spentmedia_C30Lip1_elaidicd17_1 | Huh7 media | BSA-elaidate-d17 spent media |
| SA365842 | Huh7spentmedia_C30Lip1_elaidicd17_2 | Huh7 media | BSA-elaidate-d17 spent media |
| SA365843 | Huh7spentmedia_C30Lip1_elaidicd17_3 | Huh7 media | BSA-elaidate-d17 spent media |
| SA365844 | Huh7freshmedia_C30Lip1_oleicd9_1 | Huh7 media | BSA-oleate-d9 fresh media |
| SA365845 | Huh7freshmedia_C30Lip1_oleicd9_2 | Huh7 media | BSA-oleate-d9 fresh media |
| SA365846 | Huh7freshmedia_C30Lip1_oleicd9_3 | Huh7 media | BSA-oleate-d9 fresh media |
| SA365847 | Huh7spentmedia_C30Lip1_oleicd9_1 | Huh7 media | BSA-oleate-d9 spent media |
| SA365848 | Huh7spentmedia_C30Lip1_oleicd9_2 | Huh7 media | BSA-oleate-d9 spent media |
| SA365849 | Huh7spentmedia_C30Lip1_oleicd9_3 | Huh7 media | BSA-oleate-d9 spent media |
| Showing results 1 to 12 of 12 |
Collection:
| Collection ID: | CO003473 |
| Collection Summary: | 0.75 ml of fresh media or 1.5 ml of spent media was evaporated under vacuum at 4°C and resuspended into 0.1 mL of H2O. |
| Sample Type: | Cultured cells |
Treatment:
| Treatment ID: | TR003489 |
| Treatment Summary: | Huh7 cells were treated with (1) 100 µM BSA-oleate-d9 or (2) 100 µM BSA-elaidate-d17 for 48 hours in delipidated media. |
Sample Preparation:
| Sampleprep ID: | SP003487 |
| Sampleprep Summary: | Media was spiked with 1 µg of each of the following internal standards: 15:0-18:1(d7) phosphatidylcholine (Avanti Polar Lipids, Cat #791637), 15:0-18:1(d7) phosphatidylethanolamine (Avanti Polar Lipids, Cat #791638), 18:1(d7) lysophosphatidylcholine (Avanti Polar Lipids, Cat#791643), 18:1(d7) lysophosphatidylethanolamine (Avanti Polar Lipids, Cat #791644), 15:0-18:1(d7) diacylglycerol (Avanti Polar Lipids, Cat #791647), 15:0-18:1(d7)-15:0 triacylglycerol (Avanti Polar Lipids, Cat #791648). 0.5 mL methanol, 0.5 mL H2O, and 1 mL chloroform were added directly. Samples were vortexed for 5 min and centrifuged for 5 min at 4 ˚C at 15,000g. The organic phase was collected and 2 μL of formic acid was added to the remaining polar phase which was re-extracted with 1 mL of chloroform. Combined organic phases were dried under nitrogen. After dried extracts were resuspended in 60 µl 65:30:5 ACN: IPA:H2O, 5 µL of sample was injected. |
Combined analysis:
| Analysis ID | AN005501 |
|---|---|
| Analysis type | MS |
| Chromatography type | Reversed phase |
| Chromatography system | Agilent 1260 Infinity II |
| Column | Thermo Accucore C30 (150 x 2.1mm,2.6µm) |
| MS Type | ESI |
| MS instrument type | Triple quadrupole |
| MS instrument name | Agilent 6460 QQQ |
| Ion Mode | POSITIVE |
| Units | Peak area |
Chromatography:
| Chromatography ID: | CH004183 |
| Instrument Name: | Agilent 1260 Infinity II |
| Column Name: | Thermo Accucore C30 (150 x 2.1mm,2.6µm) |
| Column Temperature: | 40°C |
| Flow Gradient: | 0 min, 30% B; 3 min, 30% B; 8 min, 43% B; 9 min, 50% B; 18 min, 90% B; 26 min, 99% B; 30 min, 99%B; 36 min, 30% B |
| Flow Rate: | 0 min, 0.1 mL/min; 8 min, 0.2 mL/min |
| Solvent A: | 60% acetonitrile/40% water; 0.1% formic acid; 10 mM ammonium formate |
| Solvent B: | 90% isopropanol/10% acetonitrile; 0.1% formic acid; 10 mM ammonium formate |
| Chromatography Type: | Reversed phase |
MS:
| MS ID: | MS005227 |
| Analysis ID: | AN005501 |
| Instrument Name: | Agilent 6460 QQQ |
| Instrument Type: | Triple quadrupole |
| MS Type: | ESI |
| MS Comments: | Lipid species were analyzed by multiple reaction monitoring of the transition from precursor to product ions at associated optimized collision energies, and fragmentor voltages using Agilent Masshunter. The m/z values of the precursor and product ions are provided in the metabolite metadata section. |
| Ion Mode: | POSITIVE |
