Adipocyte-specific tribbles pseudokinase 1 regulates plasma adiponectin and plasma lipids in mice.


Journal

Molecular metabolism
ISSN: 2212-8778
Titre abrégé: Mol Metab
Pays: Germany
ID NLM: 101605730

Informations de publication

Date de publication:
02 2022
Historique:
received: 13 08 2021
revised: 16 11 2021
accepted: 30 11 2021
pubmed: 11 12 2021
medline: 5 4 2022
entrez: 10 12 2021
Statut: ppublish

Résumé

Multiple genome-wide association studies (GWAS) have identified SNPs in the 8q24 locus near TRIB1 that are significantly associated with plasma lipids and other markers of cardiometabolic health, and prior studies have revealed the roles of hepatic and myeloid Trib1 in plasma lipid regulation and atherosclerosis. The same 8q24 SNPs are additionally associated with plasma adiponectin levels in humans, implicating TRIB1 in adipocyte biology. Here, we hypothesize that TRIB1 in adipose tissue regulates plasma adiponectin, lipids, and metabolic health. We investigate the metabolic phenotype of adipocyte-specific Trib1 knockout mice (Trib1_ASKO) fed on chow and high-fat diet (HFD). Through secretomics of adipose tissue explants and RNA-seq of adipocytes and livers from these mice, we further investigate the mechanism of TRIB1 in adipose tissue. Trib1_ASKO mice have an improved metabolic phenotype with increased plasma adiponectin levels, improved glucose tolerance, and decreased plasma lipids. Trib1_ASKO adipocytes have increased adiponectin production and secretion independent of the known TRIB1 function of regulating proteasomal degradation. RNA-seq analysis of adipocytes and livers from Trib1_ASKO mice indicates that alterations in adipocyte function underlie the observed plasma lipid changes. Adipose tissue explant secretomics further reveals that Trib1_ASKO adipose tissue has decreased ANGPTL4 production, and we demonstrate an accompanying increase in the lipoprotein lipase (LPL) activity that likely underlies the triglyceride phenotype. This study shows that adipocyte Trib1 regulates multiple aspects of metabolic health, confirming previously observed genetic associations in humans and shedding light on the further mechanisms by which TRIB1 regulates plasma lipids and metabolic health.

Identifiants

pubmed: 34890852
pii: S2212-8778(21)00270-2
doi: 10.1016/j.molmet.2021.101412
pmc: PMC8749272
pii:
doi:

Substances chimiques

Adiponectin 0
Intracellular Signaling Peptides and Proteins 0
Trib1 protein, mouse 0
Triglycerides 0
Protein Serine-Threonine Kinases EC 2.7.11.1

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

Pagination

101412

Subventions

Organisme : NHLBI NIH HHS
ID : F30 HL146076
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL141745
Pays : United States
Organisme : NIDDK NIH HHS
ID : T32 DK007328
Pays : United States

Informations de copyright

Copyright © 2021 The Authors. Published by Elsevier GmbH.. All rights reserved.

Auteurs

Elizabeth E Ha (EE)

Cardiometabolic Genomics Program, Division of Cardiology, Department of Medicine, Columbia University, New York, NY, USA.

Gabriella I Quartuccia (GI)

Cardiometabolic Genomics Program, Division of Cardiology, Department of Medicine, Columbia University, New York, NY, USA.

Ruifeng Ling (R)

Cardiometabolic Genomics Program, Division of Cardiology, Department of Medicine, Columbia University, New York, NY, USA.

Chenyi Xue (C)

Cardiometabolic Genomics Program, Division of Cardiology, Department of Medicine, Columbia University, New York, NY, USA.

Rhoda A Karikari (RA)

Institute for Diabetes and Cancer, Helmholtz Centre, Munich, Germany.

Antonio Hernandez-Ono (A)

Department of Medicine, Vagelos College of Physicians and Surgeons, Columbia University, New York, NY, USA.

Krista Y Hu (KY)

Cardiometabolic Genomics Program, Division of Cardiology, Department of Medicine, Columbia University, New York, NY, USA.

Caio V Matias (CV)

Cardiometabolic Genomics Program, Division of Cardiology, Department of Medicine, Columbia University, New York, NY, USA.

Rami Imam (R)

Cardiometabolic Genomics Program, Division of Cardiology, Department of Medicine, Columbia University, New York, NY, USA.

Jian Cui (J)

Cardiometabolic Genomics Program, Division of Cardiology, Department of Medicine, Columbia University, New York, NY, USA.

Natalia S Pellegata (NS)

Institute for Diabetes and Cancer, Helmholtz Centre, Munich, Germany.

Stephan Herzig (S)

Institute for Diabetes and Cancer, Helmholtz Centre, Munich, Germany.

Anastasia Georgiadi (A)

Institute for Diabetes and Cancer, Helmholtz Centre, Munich, Germany.

Rajesh K Soni (RK)

Proteomics and Macromolecular Crystallography Shared Resource, Herbert Irving Comprehensive Cancer Center, Columbia University, New York, NY, USA.

Robert C Bauer (RC)

Cardiometabolic Genomics Program, Division of Cardiology, Department of Medicine, Columbia University, New York, NY, USA. Electronic address: rcb36@columbia.edu.

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Classifications MeSH