PXD044020 is an
original dataset announced via ProteomeXchange.
Dataset Summary
Title | Uncoupling Metabolic Health from Thermogenesis via BCAA Flux in Brown Fat |
Description | Brown adipose tissue (BAT) is best known for thermogenesis. Whereas numerous studies in rodents found tight associations between the metabolic benefits of BAT and enhanced whole-body energy expenditure, emerging evidence in humans suggests that BAT is protective against Type 2 diabetes independent of body-weight. The underlying mechanism for this dissociation remained unclear. Here, we report that impaired mitochondrial flux of branched-chain amino acids (BCAA) in BAT, by deleting mitochondrial BCAA carrier (MBC, encoded by Slc25a44), was sufficient to cause systemic insulin resistance without affecting whole-body energy expenditure or body-weight. We found that brown adipocytes catabolized BCAAs in the mitochondria as essential nitrogen donors for the biosynthesis of glutamate, N-acetylated amino acids, and one of the products, glutathione. BAT-selective impairment in mitochondrial BCAA flux led to elevated oxidative stress and insulin resistance in the liver, accompanied by reduced levels of BCAA-nitrogen derived metabolites in the circulation. In turn, supplementation of glutathione restored insulin sensitivity of BAT-specific MBC knockout mice. Notably, a high-fat diet rapidly impaired BCAA catabolism and the synthesis of BCAA-nitrogen derived metabolites in the BAT, while cold-induced BAT activity is coupled with an active synthesis of these metabolites. Together, the present work uncovers a mechanism through which brown fat controls metabolic health independent of thermogenesis via BCAA-derived nitrogen carriers acting on the liver. |
HostingRepository | PRIDE |
AnnounceDate | 2024-02-15 |
AnnouncementXML | Submission_2024-02-15_10:14:40.166.xml |
DigitalObjectIdentifier | |
ReviewLevel | Peer-reviewed dataset |
DatasetOrigin | Original dataset |
RepositorySupport | Unsupported dataset by repository |
PrimarySubmitter | Anthony Verkerke |
SpeciesList | scientific name: Mus musculus (Mouse); NCBI TaxID: 10090; |
ModificationList | biotinylated residue |
Instrument | Orbitrap Eclipse |
Dataset History
Revision | Datetime | Status | ChangeLog Entry |
0 | 2023-07-24 01:58:55 | ID requested | |
⏵ 1 | 2024-02-15 10:14:40 | announced | |
2 | 2024-10-22 06:30:05 | announced | 2024-10-22: Updated project metadata. |
Publication List
Dataset with its publication pending |
Keyword List
submitter keyword: Brown adipose tissue (BAT), branched-chain amino acids (BCAA) |
Contact List
Shingo Kajimura |
contact affiliation | Howard Hughes Medical Institute Beth Israel Deaconess Medical Center Harvard Medical School |
contact email | skajimur@bidmc.harvard.edu |
lab head | |
Anthony Verkerke |
contact affiliation | Beth Israel Deaconess Medical Center |
contact email | averkerk@bidmc.harvard.edu |
dataset submitter | |
Full Dataset Link List
Dataset FTP location
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PRIDE project URI |
Repository Record List
[ + ]
[ - ]
- PRIDE
- PXD044020
- Label: PRIDE project
- Name: Uncoupling Metabolic Health from Thermogenesis via BCAA Flux in Brown Fat