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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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BibTeXRIS

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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