| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 2041439 | Cell Reports | 2015 | 11 Pages |
•Uptake of CoQ by brown adipocytes requires CD36•BAT lacking CD36 has a deficiency in CoQ levels•Cd36−/− BAT mitochondria display bioenergetic consequences due to CoQ deficiency•CD36 is required for nonshivering thermogenesis and normal BAT morphology
SummaryBrown adipose tissue (BAT) possesses the inherent ability to dissipate metabolic energy as heat through uncoupled mitochondrial respiration. An essential component of the mitochondrial electron transport chain is coenzyme Q (CoQ). While cells synthesize CoQ mostly endogenously, exogenous supplementation with CoQ has been successful as a therapy for patients with CoQ deficiency. However, which tissues depend on exogenous CoQ uptake as well as the mechanism by which CoQ is taken up by cells and the role of this process in BAT function are not well understood. Here, we report that the scavenger receptor CD36 drives the uptake of CoQ by BAT and is required for normal BAT function. BAT from mice lacking CD36 displays CoQ deficiency, impaired CoQ uptake, hypertrophy, altered lipid metabolism, mitochondrial dysfunction, and defective nonshivering thermogenesis. Together, these data reveal an important new role for the systemic transport of CoQ to BAT and its function in thermogenesis.
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