Department of Biochemistry and Molecular Biology, University of Southern Denmark, Odense, Denmark.
Mol Cell Biol. 2010 Aug;30(16):4077-91. doi: 10.1128/MCB.01806-08. Epub 2010 Jun 7.
The nuclear receptor peroxisome proliferator-activated receptor gamma (PPAR gamma) is essential for adipogenesis. Although several fatty acids and their derivatives are known to bind and activate PPAR gamma, the nature of the endogenous ligand(s) promoting the early stages of adipocyte differentiation has remained enigmatic. Previously, we showed that lipoxygenase (LOX) activity is involved in activation of PPAR gamma during the early stages of adipocyte differentiation. Of the seven known murine LOXs, only the unconventional LOX epidermis-type lipoxygenase 3 (eLOX3) is expressed in 3T3-L1 preadipocytes. Here, we show that forced expression of eLOX3 or addition of eLOX3 products stimulated adipogenesis under conditions that normally require an exogenous PPAR gamma ligand for differentiation. Hepoxilins, a group of oxidized arachidonic acid derivatives produced by eLOX3, bound to and activated PPAR gamma. Production of hepoxilins was increased transiently during the initial stages of adipogenesis. Furthermore, small interfering RNA-mediated or retroviral short hairpin RNA-mediated knockdown of eLOX3 expression abolished differentiation of 3T3-L1 preadipocytes. Finally, we demonstrate that xanthine oxidoreductase (XOR) and eLOX3 synergistically enhanced PPAR gamma-mediated transactivation. Collectively, our results indicate that hepoxilins produced by the concerted action of XOR and eLOX3 may function as PPAR gamma activators capable of promoting the early PPAR gamma-dependent steps in the conversion of preadipocytes into adipocytes.
过氧化物酶体增殖物激活受体 γ(PPAR γ)是脂肪生成所必需的核受体。虽然已知几种脂肪酸及其衍生物可以结合并激活 PPAR γ,但促进脂肪细胞分化早期阶段的内源性配体的性质仍然是个谜。以前,我们表明脂氧合酶(LOX)活性参与脂肪细胞分化早期阶段的 PPAR γ激活。在已知的七种鼠 LOX 中,只有非常规 LOX 表皮型脂氧合酶 3(eLOX3)在 3T3-L1 前脂肪细胞中表达。在这里,我们表明,在通常需要外源性 PPAR γ配体进行分化的条件下,强制表达 eLOX3 或添加 eLOX3 产物可刺激脂肪生成。环氧合酶,一组由 eLOX3 产生的氧化花生四烯酸衍生物,与 PPAR γ结合并激活它。在脂肪生成的初始阶段,环氧合酶的产生短暂增加。此外,eLOX3 表达的小干扰 RNA 介导或逆转录病毒短发夹 RNA 介导的敲低消除了 3T3-L1 前脂肪细胞的分化。最后,我们证明黄嘌呤氧化还原酶(XOR)和 eLOX3 协同增强了 PPAR γ 介导的转录激活。总之,我们的结果表明,XOR 和 eLOX3 的协同作用产生的环氧合酶可能作为 PPAR γ 激活剂,能够促进前脂肪细胞向脂肪细胞转化过程中早期依赖 PPAR γ 的步骤。