| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 2792528 | Cell Metabolism | 2016 | 13 Pages |
•FGF21 reduces VLDL secretion by regulating fatty acid uptake into adipose tissues•The FGF21 triglyceride-lowering effect is facilitated by CD36 and lipoprotein lipase•FGF21 increases lipoprotein disposal into adipose tissues of lean mice•In obesity, FGF21-induced lipid disposal shifts from white to brown adipose tissue
SummaryFGF21 decreases plasma triglycerides (TGs) in rodents and humans; however, the underlying mechanism or mechanisms are unclear. In the present study, we examined the role of FGF21 in production and disposal of TG-rich lipoproteins (TRLs) in mice. Treatment with pharmacological doses of FGF21 acutely reduced plasma non-esterified fatty acids (NEFAs), liver TG content, and VLDL-TG secretion. In addition, metabolic turnover studies revealed that FGF21 facilitated the catabolism of TRL in white adipose tissue (WAT) and brown adipose tissue (BAT). FGF21-dependent TRL processing was strongly attenuated in CD36-deficient mice and transgenic mice lacking lipoprotein lipase in adipose tissues. Insulin resistance in diet-induced obese and ob/ob mice shifted FGF21 responses from WAT toward energy-combusting BAT. In conclusion, FGF21 lowers plasma TGs through a dual mechanism: first, by reducing NEFA plasma levels and consequently hepatic VLDL lipidation and, second, by increasing CD36 and LPL-dependent TRL disposal in WAT and BAT.
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