Thermoneutral housing shapes hepatic inflammation and damage in mouse models of non-alcoholic fatty liver disease.


Journal

Frontiers in immunology
ISSN: 1664-3224
Titre abrégé: Front Immunol
Pays: Switzerland
ID NLM: 101560960

Informations de publication

Date de publication:
2023
Historique:
received: 15 11 2022
accepted: 27 01 2023
entrez: 6 3 2023
pubmed: 7 3 2023
medline: 8 3 2023
Statut: epublish

Résumé

Inflammation is a common unifying factor in experimental models of non-alcoholic fatty liver disease (NAFLD) progression. Recent evidence suggests that housing temperature-driven alterations in hepatic inflammation correlate with exacerbated hepatic steatosis, development of hepatic fibrosis, and hepatocellular damage in a model of high fat diet-driven NAFLD. However, the congruency of these findings across other, frequently employed, experimental mouse models of NAFLD has not been studied. Here, we examine the impact of housing temperature on steatosis, hepatocellular damage, hepatic inflammation, and fibrosis in NASH diet, methionine and choline deficient diet, and western diet + carbon tetrachloride experimental models of NAFLD in C57BL/6 mice. We show that differences relevant to NAFLD pathology uncovered by thermoneutral housing include: (i) augmented NASH diet-driven hepatic immune cell accrual, exacerbated serum alanine transaminase levels and increased liver tissue damage as determined by NAFLD activity score; (ii) augmented methionine choline deficient diet-driven hepatic immune cell accrual and increased liver tissue damage as indicated by amplified hepatocellular ballooning, lobular inflammation, fibrosis and overall NAFLD activity score; and (iii) dampened western diet + carbon tetrachloride driven hepatic immune cell accrual and serum alanine aminotransferase levels but similar NAFLD activity score. Collectively, our findings demonstrate that thermoneutral housing has broad but divergent effects on hepatic immune cell inflammation and hepatocellular damage across existing experimental NAFLD models in mice. These insights may serve as a foundation for future mechanistic interrogations focused on immune cell function in shaping NAFLD progression.

Identifiants

pubmed: 36875069
doi: 10.3389/fimmu.2023.1095132
pmc: PMC9982161
doi:

Substances chimiques

Carbon Tetrachloride CL2T97X0V0
Methionine AE28F7PNPL
Alanine Transaminase EC 2.6.1.2
Choline N91BDP6H0X

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

1095132

Subventions

Organisme : NIDDK NIH HHS
ID : R01 DK099222
Pays : United States
Organisme : NIAID NIH HHS
ID : F31 AI169757
Pays : United States
Organisme : NIDDK NIH HHS
ID : P30 DK078392
Pays : United States

Informations de copyright

Copyright © 2023 Oates, Sawada, Giles, Alarcon, Damen, Szabo, Stankiewicz, Moreno-Fernandez and Divanovic.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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Auteurs

Jarren R Oates (JR)

Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH, United States.
Division of Immunobiology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, United States.
Immunology Graduate Program, Cincinnati Children's Hospital Medical Center and the University of Cincinnati College of Medicine, Cincinnati, OH, United States.

Keisuke Sawada (K)

Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH, United States.
Division of Immunobiology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, United States.
Immunology Graduate Program, Cincinnati Children's Hospital Medical Center and the University of Cincinnati College of Medicine, Cincinnati, OH, United States.
Medical Scientist Training Program, University of Cincinnati College of Medicine, Cincinnati, OH, United States.

Daniel A Giles (DA)

Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH, United States.
Division of Immunobiology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, United States.
Immunology Graduate Program, Cincinnati Children's Hospital Medical Center and the University of Cincinnati College of Medicine, Cincinnati, OH, United States.

Pablo C Alarcon (PC)

Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH, United States.
Division of Immunobiology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, United States.
Immunology Graduate Program, Cincinnati Children's Hospital Medical Center and the University of Cincinnati College of Medicine, Cincinnati, OH, United States.
Medical Scientist Training Program, University of Cincinnati College of Medicine, Cincinnati, OH, United States.

Michelle S M A Damen (MSMA)

Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH, United States.
Division of Immunobiology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, United States.

Sara Szabo (S)

Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH, United States.
Division of Pathology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, United States.

Traci E Stankiewicz (TE)

Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH, United States.
Division of Immunobiology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, United States.

Maria E Moreno-Fernandez (ME)

Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH, United States.
Division of Immunobiology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, United States.

Senad Divanovic (S)

Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH, United States.
Division of Immunobiology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, United States.
Immunology Graduate Program, Cincinnati Children's Hospital Medical Center and the University of Cincinnati College of Medicine, Cincinnati, OH, United States.
Medical Scientist Training Program, University of Cincinnati College of Medicine, Cincinnati, OH, United States.
Center for Inflammation and Tolerance, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, United States.

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