Caloric restriction reprograms adipose tissues in rhesus monkeys
Abstract
Caloric restriction (CR) is a dietary intervention that delays the onset of age-related diseases and enhances survival in diverse organisms, and although changes in adipose tissues have been implicated in the beneficial effects of CR the molecular details are unknown. Here we show shared and depot-specific adaptations to life-long CR in subcutaneous and visceral adipose depots taken from advanced age male rhesus monkeys. Differential gene expression and pathway analysis identified key differences between the depots in metabolic, immune, and inflammatory pathways. In response to CR, RNA processing and proteostasis-related pathways were enriched in both depots but changes in metabolic, growth, and inflammatory pathways were depot-specific. Commonalities and differences that distinguish adipose depots are shared among monkeys and humans and the response to CR is highly conserved. These data reveal depot-specificity in adipose tissue adaptation that likely reflects differences in function and contribution to age-related disease vulnerability.
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Research summary
Caloric restriction induces depot-specific adaptations in adipose tissues that may influence age-related disease vulnerability. This research explores mechanisms underlying caloric restriction, which is directly related to longevity and aging by investigating how it affects adipose tissue, a key player in metabolic health and age-related diseases.
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