Adipocyte Myoglobin Is a Determinant of Energy Expenditure and a Potential Target to Limit Obesity
Year: 2026
Type: article
Abstract: Nutritional overflow and a positive energy balance are hallmarks of metabolic diseases including obesity and type 2 diabetes. Brown and beige adipocytes maintain systemic metabolic homeostasis by clearing and oxidizing energy-rich nutrients during thermogenic activation. Myoglobin (MB) is classically regarded as a muscle-associated oxygen-binding protein; however it is also expressed in brown and beige adipocytes, where it contributes to intracellular lipid handling and oxidative metabolism. Here, we report that loss of MB exclusively in adipose tissue (AT) lowers whole-body energy expenditure, impairs thermoregulation, and increases susceptibility to diet-induced obesity. AT-specific MB knockout (ATMBKO) mice exhibit elevated circulating triglycerides (TG) and fatty acids, indicating defective lipid clearance and utilization. Omics analyses reveal coordinated downregulation of oxidative phosphorylation, fatty acid metabolism, and myogenic programs. Conversely, restoration of MB in MB knockout (MBKO) mice improves metabolism in vivo. MB expression determines the capacity for mitochondrial fatty acid oxidation in brown adipocytes, whereas MB overexpression in primary human white adipocytes enhances thermogenic activity, confirming functional relevance of MB in human AT. Together, these findings establish MB as a key determinant of thermogenic lipid metabolism and energy expenditure in vivo and increasing adipocyte MB expression could increase energy expenditure and complement obesity treatment strategies.
Source: Advanced Science
DOI: 10.1002/advs.76191
Authors: Christian Strehlau, Helen Broghammer, Claudia Gebhardt, Anne Hoffmann, Tobias Hagemann, Şeyma Midilli, Rachel S. Zimmer, Kristin Schubert, Vasiliki Karagiannakou, Anastasia Georgiadi, Mario Ost, Martin Krüger, Lisa Roth, Kerstin Krause, Nora Klöting, Maria Keller, Martin Wabitsch, Rima Nuwayhid, Roland H. Stimson, Michael Stumvoll, Matthias Blüher, Juliane Weiner, John T. Heiker
Institutions: Helmholtz Munich, University Hospital Leipzig, Leipzig University, Helmholtz Centre for Environmental Research, Brandenburg University of Technology Cottbus-Senftenberg, German Center for Diabetes Research, Universität Ulm, The Queen's Medical Research Institute, University of Edinburgh
Language: English
Subfield: Physiology
Field: Medicine
Domain: Health Sciences
Open Access status: gold
Estimated APC paid: $6,730
Awards: G1455670351, SFB 1052: Mechanismen der Adipositas, G2270087404, Dissecting thermogenesis by brown adipose tissue and skeletal muscle in lean and obese subjects, G3000194542, G3368550808, Entschlüsselung der molekularen Mechanismen von Metabolismusdisruptiven Chemikalien auf die Interaktion von Adipozyten und Makrophagen, G4746016509, TRR 333: Braunes und beiges Fett Organinteraktionen, Signalwege und Energiehaushalt (BATenergy), G8719454026, MDLEICS – Leipziger Clinician Scientist Programm zu Zivilisationserkrankungen
OpenAlex ID: W7165954849
