LRG1 is an adipokine that promotes insulin sensitivity and suppresses inflammation.


Journal

eLife
ISSN: 2050-084X
Titre abrégé: Elife
Pays: England
ID NLM: 101579614

Informations de publication

Date de publication:
08 11 2022
Historique:
received: 02 07 2022
accepted: 06 11 2022
pubmed: 9 11 2022
medline: 23 11 2022
entrez: 8 11 2022
Statut: epublish

Résumé

While dysregulation of adipocyte endocrine function plays a central role in obesity and its complications, the vast majority of adipokines remain uncharacterized. We employed bio-orthogonal non-canonical amino acid tagging (BONCAT) and mass spectrometry to comprehensively characterize the secretome of murine visceral and subcutaneous white and interscapular brown adip ocytes. Over 600 proteins were identified, the majority of which showed cell type-specific enrichment. We here describe a metabolic role for leucine-rich α-2 glycoprotein 1 (LRG1) as an obesity-regulated adipokine secreted by mature adipocytes. LRG1 overexpression significantly improved glucose homeostasis in diet-induced and genetically obese mice. This was associated with markedly reduced white adipose tissue macrophage accumulation and systemic inflammation. Mechanistically, we found LRG1 binds cytochrome

Identifiants

pubmed: 36346018
doi: 10.7554/eLife.81559
pii: 81559
pmc: PMC9674348
doi:
pii:

Substances chimiques

Adipokines 0
Insulin 0
LRG1 protein, mouse 0
Glycoproteins 0

Banques de données

GEO
['GSE208219', 'GSE36026', 'GSE1133']

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : NIDDK NIH HHS
ID : RC2 DK129961
Pays : United States

Informations de copyright

© 2022, Choi et al.

Déclaration de conflit d'intérêts

CC, WB, SZ, CM, AP, MK, ZL, SS, FM, AC, TC, HM, PC No competing interests declared

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Auteurs

Chan Hee J Choi (CHJ)

Weill Cornell/Rockefeller/Sloan Kettering Tri-Institutional MD-PhD Program, New York, United States.
Laboratory of Molecular Metabolism, Rockefeller University, New York, United States.

William Barr (W)

Laboratory of Molecular Metabolism, Rockefeller University, New York, United States.

Samir Zaman (S)

Laboratory of Molecular Metabolism, Rockefeller University, New York, United States.

Corey Model (C)

Laboratory of Molecular Metabolism, Rockefeller University, New York, United States.

Annsea Park (A)

Department of Immunobiology, Yale University, New Haven, United States.

Mascha Koenen (M)

Laboratory of Molecular Metabolism, Rockefeller University, New York, United States.

Zeran Lin (Z)

Laboratory of Molecular Metabolism, Rockefeller University, New York, United States.

Sarah K Szwed (SK)

Weill Cornell/Rockefeller/Sloan Kettering Tri-Institutional MD-PhD Program, New York, United States.
Laboratory of Molecular Metabolism, Rockefeller University, New York, United States.

Francois Marchildon (F)

Laboratory of Molecular Metabolism, Rockefeller University, New York, United States.

Audrey Crane (A)

Laboratory of Molecular Metabolism, Rockefeller University, New York, United States.

Thomas S Carroll (TS)

Bioinformatics Resouce Center, Rockefeller University, New York, United States.

Henrik Molina (H)

Proteomics Resource Center, Rockefeller University, New York, United States.

Paul Cohen (P)

Laboratory of Molecular Metabolism, Rockefeller University, New York, United States.

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Classifications MeSH