Turning off the furnace: the intracellular brake systems for brown fat thermogenesis

Projektinformationen

BATOFF

ID Finanzhilfevereinbarung: 101078516

DOI

10.3030/101078516

EK-Unterschriftsdatum 28 Juli 2023

Startdatum 1 Januar 2024

Enddatum 31 Dezember 2028

Finanziert unter

• European Research Council (ERC)

Gesamtkosten

€ 1 499 526,25

EU-Beitrag

€ 1 499 526,00

Koordiniert durch

UNIVERSITATSKLINIKUM BONN
Germany

Periodic Reporting for period 1 - BATOFF (Turning off the furnace: the intracellular brake systems for brown fat thermogenesis)

Berichtszeitraum: 2024-01-01 bis 2026-06-30

Zusammenfassung vom Kontext und den Gesamtzielen des Projekts

Free-ranging animals are continuously exposed to fluctuating ambient temperatures, making rapid and precise adjustment of thermogenesis essential for maintaining core body temperature homeostasis and ensuring survival. Brown adipose tissue (BAT) has evolved as a specialized thermogenic organ, in which rapid activation and deactivation of heat production is critical for effective thermal regulation in response to environmental changes.

Importantly, thermogenesis is inherently associated with a high energetic cost, and BAT therefore functions as a metabolically expensive, energy-dissipating tissue. From an evolutionary perspective, it is likely that mechanisms limiting unnecessary BAT activation have been strongly favored by natural selection in order to preserve metabolic efficiency and energy thriftiness. Such a constrained regulatory strategy would ensure that thermogenesis is engaged only when strictly required.

However, this fundamental concept, as well as the molecular mechanisms that impose constraints on BAT activity, remain poorly understood and largely unexplored. Elucidating these endogenous regulatory brakes represents a critical knowledge gap in the field. Addressing this gap will not only advance our understanding of thermogenic control but also open new avenues to unlock and harness the full energy-dissipating potential of BAT for therapeutic applications in metabolic disease.

Arbeit, die ab Beginn des Projekts bis zum Ende des durch den Bericht erfassten Berichtszeitraums geleistet wurde, und die wichtigsten bis dahin erzielten Ergebnisse

The BATOFF project aims to uncover the fundamental principles governing the negative regulation of brown adipose tissue (BAT) thermogenesis by identifying intrinsic molecular “brake” systems that limit its energy-dissipating capacity and ensure precise control of heat production. In the past two years, we have conducted extensive work across all three aims (AIM1-3) of the project.

For AIM1, we have investigated the molecular regulation and functional significance of compartmentalized cAMP signaling mediated by phase separation processes in brown adipocyte thermogenesis, thereby providing mechanistic insight into how localized signaling controls thermogenic activation.

For AIM2, we have completed the in vitro experiments and successfully established genetically modified mouse models, including adipocyte-specific conditional knockouts and whole-body knockout models, enabling the extension of our studies into physiologically relevant in vivo systems.

For AIM3, we have performed both loss- and gain-of-function analyses of key purine nucleotide metabolic pathways to investigate their roles in constraining UCP1 activity. In parallel, we have developed a UCP1 functional analysis system that enables ectopic expression of mutant UCP1 in UCP1-deficient adipocytes, allowing systematic screening of variants to define structure–function relationships and their impact on thermogenic activity.

Building on these three synergistic mechanisms—a phase separation–mediated process, a lipolysis-driven feedforward circuit with embedded negative feedback, and a purinergic nucleotide–dependent inhibitory pathway—this work defines a coordinated regulatory framework that constrains BAT activity.

Fortschritte, die über den aktuellen Stand der Technik hinausgehen und voraussichtliche potenzielle Auswirkungen (einschließlich der bis dato erzielten sozioökonomischen Auswirkungen und weiter gefassten gesellschaftlichen Auswirkungen des Projekts)

The work performed within the BATOFF project has advanced the field beyond the current state of the art by uncovering previously unrecognized mechanisms that constrain brown adipose tissue (BAT) thermogenesis. First, we provide new mechanistic insight into how spatial organization of cAMP signaling through phase separation processes regulates thermogenic activation in brown adipocytes, revealing a higher-order layer of signal compartmentalization not captured by classical linear signaling models.

Second, we have established a new conceptual framework for BAT regulation by identifying interconnected regulatory “brake” systems that integrate signaling dynamics, lipid metabolism, and nucleotide-dependent inhibitory pathways. This systems-level view moves beyond single-pathway control and instead defines thermogenesis as the outcome of tightly coordinated positive and negative regulatory circuits.

Third, we have generated and validated novel in vitro and in vivo model systems, including genetically modified mouse models and a dedicated UCP1 functional screening platform. These tools enable direct functional interrogation of thermogenic regulators and mutant UCP1 variants in a physiologically relevant context, providing a scalable framework for structure–function analysis.

Collectively, these advances challenge the prevailing view of BAT as a predominantly activation-driven thermogenic system and instead establish the concept that thermogenesis is actively constrained by multiple endogenous molecular brake mechanisms. This work therefore opens new conceptual and methodological avenues to therapeutically modulate BAT activity in metabolic disease.