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Thyroid hormones are required for thermogenesis of beige adipocytes induced by Zfp423 inactivation

Lisa Roth, Anne Hoffmann, Tobias Hagemann, Leonie Wagner, Christian Strehlau, Bilal Sheikh, Lorenz Donndorf, Adhideb Ghosh, Falko Noé, Christian Wolfrum, Knut Krohn, Juliane Weiner, John T. Heiker, Nora Klöting, Michael Stumvoll, Anke Tönjes, Matthias Blüher, Jens Mittag, Kerstin Krause*

*Korrespondierende/r Autor/-in für diese Arbeit

Abstract

The significance of thyroid hormones (THs) in beige adipocyte thermogenesis remains incompletely understood. We previously reported that THs directly regulate the expression of zinc-finger protein 423 (ZFP423), an anti-thermogenic factor, in adipose tissue. This study investigates the interaction between THs and adrenergic signaling in regulating thermogenic capacity and activation of beige adipocytes formed in response to Zfp423 deletion. We demonstrate that THs are indispensable for uncoupling protein 1 (UCP1)-dependent thermogenesis, leading to increased energy expenditure in mice with adipocyte-specific Zfp423 knockout. Targeted activation of the thyroid receptor isoform TRβ, which plays a central role in the inguinal depot, is sufficient to enhance energy expenditure in hypothyroid Zfp423iAKO mice. Mechanistically, THs and ZFP423 pathways cooperate to regulate early B cell factor 2 (EBF2)-mediated activation of the Ucp1 gene. RNA sequencing (RNA-seq) analysis of human adipose tissue samples supports the relevance of this regulatory network for human adipose tissue plasticity.

OriginalspracheEnglisch
Aufsatznummer114987
ZeitschriftCell Reports
Jahrgang43
Ausgabenummer12
ISSN2639-1856
DOIs
PublikationsstatusVeröffentlicht - 24.12.2024

UN SDGs

Dieser Output leistet einen Beitrag zu folgendem(n) Ziel(en) für nachhaltige Entwicklung

  1. SDG 3 – Gesundheit und Wohlergehen
    SDG 3 – Gesundheit und Wohlergehen

Strategische Forschungsbereiche und Zentren

  • Forschungsschwerpunkt: Gehirn, Hormone, Verhalten - Center for Brain, Behavior and Metabolism (CBBM)

DFG-Fachsystematik

  • 2.22-17 Endokrinologie, Diabetologie, Metabolismus

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