Summary of project PR001305

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 PR001305. The data can be accessed directly via it's Project DOI: 10.21228/M81H6N This work is supported by NIH grant, U2C- DK119886.

See: https://www.metabolomicsworkbench.org/about/howtocite.php

Project ID: PR001305
Project DOI:doi: 10.21228/M81H6N
Project Title:Glutamine Flux analysis in Macrophages
Project Type:MS quantitive analysis
Project Summary:To determine the effect of Sirt3 K223R on glutaminolysis, we traced glutamine metabolic influx in macrophages. The data demonstrated that Sirt3 K223R did not alter glutamine uptake and glutamate production in BMDMs after IL-4 treatment . However, 5C(M+5) labeled-αKG showed a higher ratio in IL-4-treated Sirt3 KR macrophages than that in IL-4-treated Sirt3 WT macrophages, suggesting that SENP1-Sirt3 axis mainly involves the conversion of glutamate to αKG of glutaminolysis in macrophage M2 polarization.
Institute:Shanghai Jiao Tong University affiliated Renji Hospital
Department:Department of Urology
Laboratory:Cheng Jinke's Lab
Last Name:Zhou
First Name:Wei
Address:N0.280 South Chongqing Road
Email:joesphchou@alumni.sjtu.edu.cn
Phone:+8615216716293
Funding Source:National Natural Science Foundation of China
Project Comments:In summary, we reveal that SENP1-Sirt3 signaling plays a crucial role in promoting αKG production and M2 polarization.
Publications:Cell Reports
Contributors:Wei Zhou

Summary of all studies in project PR001305

Study IDStudy TitleSpeciesInstituteAnalysis
(* : Contains Untargted data)
Release
Date
VersionSamplesDownload
(* : Contains raw data)
ST002061 Glutamine flux in macrophages treated with stable-isotope labeled analog 4 mM (U-13C5) glutamine Mus musculus Shanghai Jiao Tong University affiliated Renji Hospital MS 2022-02-07 1 16 Uploaded data (251.3M)*
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