Quercetin rejuvenates aged adipose progenitor cells by attenuating inflammatory pathways.
Abstract
The mass of inguinal white adipose tissue (iWAT) decreases with age, and its dysfunction contributes to systemic effects, including chronic inflammation, ectopic lipid deposition, and insulin resistance. However, the molecular and functional characteristics of aged adipose progenitor cells (APCs), as well as effective strategies to rejuvenate their adipogenic potential, remain poorly understood. In this study, we found that aged mice exhibited a reduced frequency of APCs, increased inflammatory activity, and impaired adipogenic differentiation capacity. Strikingly, while quercetin exerted concentration-dependent effects on the vitality and function of APCs, only moderate doses specifically restored the adipogenic differentiation of aged APCs. Mechanistically, this rejuvenating effect was primarily mediated through the suppression of pro-inflammatory pathways. Together, our findings provide novel mechanistic insights into APCs aging in iWAT and identify quercetin as a promising rejuvenative agent for the treatment of adipose tissue dysfunction and related metabolic disorders in aging.
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Research summary
Quercetin restores the adipogenic differentiation capacity of aged adipose progenitor cells by suppressing inflammatory pathways. This study addresses the aging process at a cellular level, focusing on rejuvenating progenitor cells, which is directly relevant to understanding and potentially mitigating age-related dysfunctions.
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