Why the study?
Impaired white adipose tissue remodeling occurs in obesity and aging, but the underlying mechanisms of adipogenesis defects and their therapeutic potential require clarification to address obesity- and age-related disorders.
This review highlights the mechanisms of white adipose tissue maladaptation in obesity and aging, suggesting adipocyte-targeted therapies for related disorders.
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Adipogenesis defects may underlie impaired WAT expansion in hypertrophic obesity; leaves open causal mechanisms and targets in humans.
The adipose organ adapts and responds to internal and environmental stimuli by remodeling both its cellular and extracellular components. Under conditions of energy surplus, the subcutaneous white adipose tissue (WAT) is capable of expanding through the enlargement of existing adipocytes (hypertrophy), followed by de novo adipogenesis (hyperplasia), which is impaired in hypertrophic obesity. However, an impaired hyperplastic response may result from various defects in adipogenesis, leading to different WAT features and metabolic consequences, as discussed here by reviewing the results of the studies in animal models with either overexpression or knockdown of the main molecular regulators of the two steps of the adipogenesis process. Moreover, impaired WAT remodeling with aging has been associated with various age-related conditions and reduced lifespan expectancy. Here, we delve into the latest advancements in comprehending the molecular and cellular processes underlying age-related changes in WAT function, their involvement in common aging pathologies, and their potential as therapeutic targets to influence both the health of elderly people and longevity. Overall, this review aims to encourage research on the mechanisms of WAT maladaptation common to conditions of both excessive and insufficient fat tissue. The goal is to devise adipocyte-targeted therapies that are effective against both obesity- and age-related disorders.
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Iacobini et al. (2024) studied this question.
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