Macrophage-derived itaconate acts as a paracrine signal to repress adipose tissue thermogenesis by antagonizing the uptake of the pro-thermogenic metabolite succinate into brown adipose tissue.
Thermogenic brown and beige adipose tissues are important in maintaining metabolic health because of their distinct ability to catabolize stored fat and circulating glucose in futile cycles1,2. Macrophages, present in brown adipose tissue, have been reported to both positively and negatively regulate thermogenic adipocyte function through mechanisms that are incompletely understood3–14. Here we show that the macrophage-derived metabolite, itaconate, acts as a paracrine signal to repress adipose tissue thermogenesis in mice. Mechanistically, itaconate inhibits thermogenesis by antagonizing uptake of the pro-thermogenic metabolite, succinate, into brown adipose tissue. These findings reveal an unexpected mechanism for local control of thermogenesis in vivo that relies on paracrine itaconate signalling and demonstrate that the important signalling roles of itaconate extend beyond immunological processes to the regulation of energy balance. Tang et al. reveal that macrophage-derived itaconate acts as a paracrine inhibitor of adipose tissue thermogenesis by blocking succinate uptake into brown adipose tissue.
“This study we show that macrophage-derived itaconate acts as a paracrine signal that suppresses brown adipose tissue thermogenesis by competing with the pro-thermogenic metabolite succinate for uptake through the MCT1 transporter. By limiting succinate uptake into brown adipocytes, macrophages directly restrain mitochondrial respiration and heat production. Revealing an intriguing form of metabolic communication between immune cells and adipose tissue!”
Tang et al. (Tue,) conducted a letter in Adipose tissue thermogenesis. Itaconate vs. Vehicle or control mice was evaluated on Thermogenesis (energy expenditure and body temperature). Macrophage-derived itaconate acts as a paracrine signal to repress adipose tissue thermogenesis by antagonizing the uptake of the pro-thermogenic metabolite succinate into brown adipose tissue.
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