Key result
Human cell culture models better recapitulate obesity-related dysfunction than animal models when studying adipogenesis.
Why the study?
The rising prevalence of obesity and its metabolic consequences have intensified focus on adipose tissue biology, adipocyte proliferation, and adipogenesis to better understand adipocyte dysfunction and metabolic complications.
This review provides practical guidance on selecting appropriate in vitro cell models for studying adipogenesis and obesity-related metabolic complications.
May guide in vitro model selection for obesity research; leaves open clinical translation pending prospective validation.
The prevalence of obesity and its metabolic consequences have prompted researchers to pay more attention to adipose tissue biology, the mechanisms driving adipocyte proliferation, and the process of adipogenesis. The development of diverse in vitro cell models and molecular biology techniques has made it possible to investigate adipocyte commitment and differentiation, which are complex processes underlying adipose tissue function. These approaches enable a better understanding of adipocyte dysfunction and adipogenesis associated with obesity and its metabolic complications. To mimic white, beige, and brown adipocytes, researchers have established different cell models from animals and humans with adipogenic capacity. In this review, we have compiled and updated information on animal and human cell culture models used to study in vitro adipogenesis, including their main characteristics, protocols, and applications. We provide practical guidance on model selection for specific obesity-related questions such as insulin resistance, inflammation, browning, and depot-specific dysfunction. Additionally, we discuss co-cultures and three-dimensional culture systems, highlighting their value in creating a more physiological environment and elucidating the interactions between adipocytes and neighboring cells • Murine cell models ensure reproducibility but show species-specific differences to human models, which better recapitulate obesity-related metabolic dysfunction. • Human cell lines and primary adipose stem and progenitor cells (ASPCs) capture depot- and donor-specific adipose traits. • 3D and co-culture adipose models better reproduce tissue complexity and intercellular crosstalk.
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Núñez-Sánchez et al. (2026) conducted a review in Obesity and metabolic consequences. In vitro cell models (animal and human) was evaluated. Animal and human cell culture models, including 3D and co-culture systems, provide valuable tools for studying adipogenesis, with human models better recapitulating obesity-related dysfunction.
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