Summary of Study ST000924

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 PR000640. The data can be accessed directly via it's Project DOI: 10.21228/M8Z40Z This work is supported by NIH grant, U2C- DK119886.

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Study IDST000924
Study TitleMuRF1-Related Metabolic Alterations in HL-1 Cardiomyocyte Induced by Cyclic Stretch
Study TypeCardiomyocyte cell culture
Study SummaryWe collected cell media and performed GC-MS non-targeted metabolomics to identify the role of MuRF1 in the dynamic metabolic changes in cardiomyocytes.
Institute
University of North Carolina at Chapel Hill
DepartmentPathology & Laboratory Medicine
LaboratoryWillis
Last NameWillis
First NameMonte
Address111 Mason Farm Road
Emailmonte_willis@med.unc.edu
Phone9849995431
Submit Date2017-10-30
Num Groups6
Total Subjects32
Raw Data AvailableYes
Raw Data File Type(s)d
Analysis Type DetailLC-MS
Release Date2018-12-11
Release Version1
Monte Willis Monte Willis
https://dx.doi.org/10.21228/M8Z40Z
ftp://www.metabolomicsworkbench.org/Studies/ application/zip

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Treatment:

Treatment ID:TR000976
Treatment Summary:Cell culture, adenovirus transduction, and MuRF1 knock-down. The cardiomyocyte-derived HL-1 cell line was maintained as previously described [11-13]. Briefly, cells were split and cultured to ~90% confluency in 6-well BioFlex culture plates (Flexcell International Corporation, Hillsborough, NC) coated with 0.02% gelatin (wt/vol) and 0.5% fibronectin (vol/vol) for ∼30 min and grown in complete Claycomb media containing 10% serum (Cat. #51800C, Sigma-Aldrich; St. Louis, MO), as previously described [13]. Media was changed to serum-free Dulbecco’s modified Eagle’s medium (DMEM) supplemented 1% penicillin-streptomycin. HL-1 cells were transduced with 30 MOI adenovirus expressing shRNA MuRF1 (Ad.shRNA MuRF1) or shRNA scramble (Ad.shRNA Scr) control (custom made by Vector Biolabs, Philadelphia, PA) to transiently knock down MuRF1, as previously described [13].
Treatment:Ad.shRNA MuRF1 (or Ad.shRNA Scramble) treatment
Treatment Compound:Adenovirus
Treatment Route:Media
Treatment Dose:30 MOI
Treatment Dosevolume:<10 ul
Treatment Doseduration:48 hours
Treatment Vehicle:DMEM
Cell Media:DMEM / No serum
Cell Envir Cond:Stretch
Cell Pct Confluence:~60%
Cell Media Lastchanged:At start of stretch period.
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