bioRxiv · 10.1101/2025.09.25.678284
Adipose tissue cell states linked to progression and clinical subtypes of MASLD in human obesity
Abstract
Adipose tissue dysfunction is a key determinant of inter-individual variability in obesity-associated comorbidities, yet the underlying tissue-level mechanisms linking adipose remodeling to progression of metabolic dysfunction-associated steatotic liver disease (MASLD) remain poorly defined. We applied single-nucleus RNA sequencing to abdominal subcutaneous adipose tissue (SAT) from individuals with severe obesity, stratified by histologically defined MASLD stage, and integrated these data with bulk RNA-seq from [~]200 individuals. MASLD was associated with adipocyte hypertrophy and near-depletion of an ADH1BHI adipocyte subset linked to improved lipid buffering and systemic metabolic health. Conversely, lipid-associated macrophages (LAMs) expanded in MASLD, coordinating lipid-handling and inflammatory programs in the myeloid compartment. In advanced metabolic dysfunction-associated steatohepatitis (MASH), we identified a senescence-associated PLAUHI progenitor subpopulation with pro-inflammatory signaling potential. Whereas LAMs were broadly enriched in MASLD subtypes, PLAUHI progenitors specifically marked a cardiometabolic MASLD endotype, characterized by type 2 diabetes and cardiovascular disease. These findings highlight cellular remodeling of adipose tissue as a potential driver of MASLD heterogeneity and progression.
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Madsen, J. D., Dam, T. V., Nambiar, J., Liang, C., Peltonen, A. R., Wernberg, C. W., Rydbirk, R., Oussoren, L. M. K., Jakobsen, K. S., Klinggaard, E. G., Hansen, D., Maniyadath, B., Jonasson, E., Caterino, T. D., Krag, A., Ravnskjaer, K., Mandrup, S., Lauridsen, M. E. M., Loft, A., Schmidt, S. F.. 2025-09-29. Adipose tissue cell states linked to progression and clinical subtypes of MASLD in human obesity. https://doi.org/10.1101/2025.09.25.678284
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