Laboratory of Physiological Chemistry, Institute of Medicinal Chemistry, Hoshi University, Shinagawa, Tokyo 142-8501, Japan.
Biochem Biophys Res Commun. 2013 Mar 29;433(1):102-7. doi: 10.1016/j.bbrc.2013.02.057. Epub 2013 Feb 26.
Retinoic acid (RA) signaling is mediated by specific nuclear hormone receptors. Here we examined the effects of 9-cis-RA on adipogenesis in mouse preadipocyte 3T3-L1 cells. 9-cis-RA inhibits the lipid accumulation of adipogenetically induced 3T3-L1 cells. The complex of retinoid X receptor α (RXRα) with peroxisome proliferator-activated receptor γ (PPARγ) is a major transcription factor in the process of adipogenesis, and the levels of these molecules were decreased by 9-cis-RA treatment. A RXR pan-antagonist suppressed 9-cis-RA's inhibitory effects on adipogenesis, but not on the intracellular levels of both RXRα and PPARγ. These results suggest that 9-cis-RA could inhibit adipogenesis by activating RXR, and decrease both RXR and PPARγs levels in a RXR activation-independent manner.
视黄酸(RA)信号转导是由特定的核激素受体介导的。在这里,我们研究了 9-顺式-视黄酸(9-cis-RA)对小鼠前体脂肪细胞 3T3-L1 细胞脂肪生成的影响。9-cis-RA 抑制诱导脂肪生成的 3T3-L1 细胞的脂质积累。视黄酸 X 受体 α(RXRα)与过氧化物酶体增殖物激活受体 γ(PPARγ)的复合物是脂肪生成过程中的主要转录因子,而这些分子的水平在 9-cis-RA 处理后降低。RXR 泛拮抗剂抑制了 9-cis-RA 对脂肪生成的抑制作用,但不抑制 RXRα 和 PPARγ 的细胞内水平。这些结果表明,9-cis-RA 可以通过激活 RXR 抑制脂肪生成,并以 RXR 激活不依赖的方式降低 RXR 和 PPARγs 的水平。