Mechanobiology of Adipose Tissue Remodeling

Adipose tissue is a highly plastic organ whose remodeling dynamics are central to whole-body metabolic health. Expansion of white adipose tissue occurs through either hyperplasia, which preserves tissue function, or hypertrophy, which causes local hypoxia, inflammation, and pathological extracellular matrix (ECM) accumulation. Under hypertrophic conditions, the ECM stiffens and transitions from a supportive scaffold to a fibrotic barrier that limits expansion and perpetuates metabolic dysfunction. Understanding how mechanical cues regulate adipose tissue remodeling is, therefore, essential for identifying new therapeutic strategies. Two mechanosensitive cell populations, adipose stem cells (ASC) and mature adipocytes, are central to this process. ASC interpret ECM stiffness and compositional changes, which determine lineage outcomes. Soft and flexible matrices favor adipogenesis, whereas stiff matrices drive fibroblast-like activation and matrix deposition. Adipocytes, though differentiated, retain mechanosensitive signaling capabilities that shape their function. Under chronic mechanical stresses, cytoskeletal remodeling pathways lead to changes in gene expression and partial dedifferentiation toward a fibroblast-like phenotype. Reciprocal signaling between ASC and adipocytes amplifies these processes, establishing feedback loops that reinforce either healthy or pathological remodeling. Cell and tissue engineering approaches are essential for dissecting these processes, with hydrogel substrates, 3D scaffolds, compression assays, and atomic force microscopy offering physiologically relevant platforms to model progenitors and adipose tissue cellular mechanics. Emerging tools, including nanotopography and mechanical stimulation devices, have the capacity to further clarify how mechanical signals influence adipose remodeling. By positioning ASC and adipocytes as active regulators of ECM mechanics, we underscore the importance of mechanotransduction pathways in adipose tissue health and point to bioengineering strategies that may help discover ways to restore tissue flexibility and improve metabolic outcomes.

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Publication Details

Journal
Tissue Engineering Part A
Published
2025-12-19
DOI
https://doi.org/10.1177/19373341251405218
Citations
1
Primary Topic
Adipokines, Inflammation, and Metabolic Diseases
Type
article
Field-Weighted Citation Impact
1.35
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article

Mechanobiology of Adipose Tissue Remodeling

Scott P. Connelly, Matthew D. Layne, Cheyanne L. Frosti
1 citations
Tissue Engineering Part A
Adipokines, Inflammation, and Metabolic Diseases
1.35
article

Mechanobiology of Adipose Tissue Remodeling

Scott P. Connelly, Matthew D. Layne, Cheyanne L. Frosti
article en
1 citations

Abstract

Adipose tissue is a highly plastic organ whose remodeling dynamics are central to whole-body metabolic health. Expansion of white adipose tissue occurs through either hyperplasia, which preserves tissue function, or hypertrophy, which causes local hypoxia, inflammation, and pathological extracellular matrix (ECM) accumulation. Under hypertrophic conditions, the ECM stiffens and transitions from a supportive scaffold to a fibrotic barrier that limits expansion and perpetuates metabolic dysfunction. Understanding how mechanical cues regulate adipose tissue remodeling is, therefore, essential for identifying new therapeutic strategies. Two mechanosensitive cell populations, adipose stem cells (ASC) and mature adipocytes, are central to this process. ASC interpret ECM stiffness and compositional changes, which determine lineage outcomes. Soft and flexible matrices favor adipogenesis, whereas stiff matrices drive fibroblast-like activation and matrix deposition. Adipocytes, though differentiated, retain mechanosensitive signaling capabilities that shape their function. Under chronic mechanical stresses, cytoskeletal remodeling pathways lead to changes in gene expression and partial dedifferentiation toward a fibroblast-like phenotype. Reciprocal signaling between ASC and adipocytes amplifies these processes, establishing feedback loops that reinforce either healthy or pathological remodeling. Cell and tissue engineering approaches are essential for dissecting these processes, with hydrogel substrates, 3D scaffolds, compression assays, and atomic force microscopy offering physiologically relevant platforms to model progenitors and adipose tissue cellular mechanics. Emerging tools, including nanotopography and mechanical stimulation devices, have the capacity to further clarify how mechanical signals influence adipose remodeling. By positioning ASC and adipocytes as active regulators of ECM mechanics, we underscore the importance of mechanotransduction pathways in adipose tissue health and point to bioengineering strategies that may help discover ways to restore tissue flexibility and improve metabolic outcomes.

Tissue Engineering Part A
Boston University (US)
Openalex Percentile: Top 13%
Adipokines, Inflammation, and Metabolic Diseases
1.35
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