Key result
Thyroid hormones are indispensable for UCP1-dependent thermogenesis and increased energy expenditure in beige adipocytes induced by Zfp423 inactivation.
Why the study?
The significance of thyroid hormones in beige adipocyte thermogenesis remains incompletely understood.
Thyroid hormones are crucial for activating beige adipocyte thermogenesis induced by Zfp423 inactivation, providing insight into regulatory mechanisms for systemic energy metabolism.
Thyroid hormone requirement for beige activation warrants caution in metabolic interventions; leaves open human translation and cardiometabolic trials.
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.
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Roth et al. (2024) studied Obesity (n=1,202). Thyroid hormone signaling and Zfp423 inactivation vs. Control / Euthyroid status was evaluated on UCP1-dependent thermogenesis and energy expenditure. Thyroid hormones are indispensable for UCP1-dependent thermogenesis and increased energy expenditure in beige adipocytes induced by Zfp423 inactivation.
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