| Popis: |
/ SUMMARYProstaglandins play fundamental roles in adipose tissue function. While prostaglandin F2α inhibits adipogenesis, prostaglandin E2 promotes adipose beiging. PGF2α and PGE2 are both inactivated through uptake by the plasma membrane transporter (PGT). We hypothesized that inhibiting PGT would increase PGF2α and PGE2 levels, thereby reducing white fat expansion and inducing beiging. Consistent with this hypothesis, inhibiting PGT in mice on high fat diet via genetic knockout or pharmacological blockade reduced body fat stores and induced thermogenesis at thermoneutrality. Inguinal white adipose tissue (iWAT) of these mice exhibited robust UCP1-independent thermogenesis characterized by mitochondrial expansion, coupling of O2 consumption to ATP synthesis, and induction of the creatine pathway. Enhanced coupled respiration persisted in PGT-KO iWAT adipocytes in a creatine shuttle-dependent manner. Thus, inhibiting PGT increases mitochondrial biogenesis and coupled respiration—each supported by the creatine pathway in a system lacking UCP1 expression—revealing PGT as a promising drug target against obesity. |
