Cytoarchitectural multi-depot profiling reveals immune-metabolic crosstalk in human colon-associated adipose tissue

While it is well established that the cellular composition of white adipose tissue (WAT) varies between depots, the functional relevance of this heterogeneity remains unclear. By combining spatial and single-nucleus RNA sequencing, we provide a comprehensive map of subcutaneous and visceral (omental, mesenteric, mesocolic, and epiploic) WAT in both men and women. Our analyses reveal shared features, such as the spatial organization of adipogenesis, alongside depot-specific characteristics, including distinct cell-type enrichments and unique cell-cell communication routes. Epiploic WAT stands out by harboring high proportions of serum amyloid A expressing fat cells (encoded by SAA1/SAA2) and several leukocyte populations. Through mechanistic studies, we demonstrate that adipocyte SAA1/SAA2 expression is induced by inflammatory signals, including lipopolysaccharide, and that SAA1 activates immune responses in adipose-resident myeloid cells. Collectively, our findings suggest that visceral WAT exhibits distinct cytoarchitectural properties, with those located near the colon adapting by developing specialized adipocytes and immune cell populations.

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Publication Details

Journal
Cell Metabolism
Published
2026-01-13
DOI
https://doi.org/10.1016/j.cmet.2025.12.008
Citations
2
Primary Topic
Adipokines, Inflammation, and Metabolic Diseases
Type
article
Field-Weighted Citation Impact
63.04
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article

Cytoarchitectural multi-depot profiling reveals immune-metabolic crosstalk in human colon-associated adipose tissue

William Gourash, Lucas Massier, Joanna Kalucka, Jutta Jalkanen et al.
2 citations
Cell Metabolism
Adipokines, Inflammation, and Metabolic Diseases
63.04
article

Cytoarchitectural multi-depot profiling reveals immune-metabolic crosstalk in human colon-associated adipose tissue

William Gourash, Lucas Massier, Joanna Kalucka, Jutta Jalkanen, Benedek Pesti, Marcus Buggert, Nayanika Bhalla, Niklas Mejhert, Merve Elmastas, Jesper Bäckdahl, Patrik L. Ståhl, Arne Dietrich, Mikael Rydén, Jiawei Zhong, Margo P. Emont, Zinger Yang Loureiro, Pamela A. Nono Nankam, Sophie Weinbrenner, Anders Thorell, Anita Courcoulas, Matthias Blüher, Jiaxin Luo, Scott Frendo-Cumbo, Evan D. Rosen, Peter Kovacs
article en
2 citations

Abstract

While it is well established that the cellular composition of white adipose tissue (WAT) varies between depots, the functional relevance of this heterogeneity remains unclear. By combining spatial and single-nucleus RNA sequencing, we provide a comprehensive map of subcutaneous and visceral (omental, mesenteric, mesocolic, and epiploic) WAT in both men and women. Our analyses reveal shared features, such as the spatial organization of adipogenesis, alongside depot-specific characteristics, including distinct cell-type enrichments and unique cell-cell communication routes. Epiploic WAT stands out by harboring high proportions of serum amyloid A expressing fat cells (encoded by SAA1/SAA2) and several leukocyte populations. Through mechanistic studies, we demonstrate that adipocyte SAA1/SAA2 expression is induced by inflammatory signals, including lipopolysaccharide, and that SAA1 activates immune responses in adipose-resident myeloid cells. Collectively, our findings suggest that visceral WAT exhibits distinct cytoarchitectural properties, with those located near the colon adapting by developing specialized adipocytes and immune cell populations.

Cell MetabolismVol. 38(2)
Beth Israel Deaconess Medical Center (US), Karolinska University Hospital (SE), Helmholtz Centre for Environmental Research (DE), Aarhus University (DK), Science for Life Laboratory (SE), Karolinska Institutet (SE), University of Chicago (US), Glanrhyd Hospital (GB), Integrated Cardio Metabolic Centre (SE), University Hospital Leipzig (DE), University of Pittsburgh Medical Center (US), KTH Royal Institute of Technology (SE), Leipzig University (DE)
Openalex Percentile: Top 0%
Adipokines, Inflammation, and Metabolic Diseases
63.04
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