Moriyama Ryutaro, Yamazaki Tsubasa, Kato Takako, Kato Yukio
Laboratory of Environmental Physiology, Department of Life Science, School of Science and Engineering, Kinki University, Osaka 577-8502, Japan.
J Reprod Dev. 2016 Apr 22;62(2):195-9. doi: 10.1262/jrd.2015-138. Epub 2016 Feb 5.
Here, we assessed the effects of long-chain fatty acids (LCFAs) and the LCFA receptor agonist GW9508 on the transcription of the gonadotropin subunit genes Cga, Lhb and Fshb because LCFA receptor GPR120 was observed in mouse gonadotropes in our recent study. A transcription assay using LβT2 cells demonstrated that LCFAs, oleic acid, α-linolenic acid, docosahexaenoic acid and palmitate, repressed the expression of Cga, Lhb, and Fshb at concentrations between 50 and 100 µM. On the other hand, treatment with 10 µM unsaturated LCFAs, oleic acid, α-linolenic acid and docosahexaenoic acid, repressed only Fshb expression, while the same dose of a saturated LCFA, palmitate, had no effect on the expression of gonadotropin subunit genes. Furthermore, GW9508 did not affect promoter activity. Next, we examined deletion mutants of the upstream region of Fshb and found that the upstream regulatory region (-2824 to -2343 bp) of Fshb was responsible for the notable repression by 10 µM unsaturated LCFAs. Our results suggest that the upstream region of Fshb is susceptible to unsaturated LCFAs. In addition, unsaturated LCFAs play a role in repressing Fshb expression through the distal -2824 to -2343 bp region, which might be independent of the LCFA receptor GPR120 pathway.
在此,我们评估了长链脂肪酸(LCFAs)和LCFA受体激动剂GW9508对促性腺激素亚基基因Cga、Lhb和Fshb转录的影响,因为我们最近的研究在小鼠促性腺激素细胞中观察到了LCFA受体GPR120。使用LβT2细胞进行的转录分析表明,LCFAs、油酸、α-亚麻酸、二十二碳六烯酸和棕榈酸在50至100μM的浓度下可抑制Cga、Lhb和Fshb的表达。另一方面,用10μM不饱和LCFAs、油酸、α-亚麻酸和二十二碳六烯酸处理仅抑制Fshb的表达,而相同剂量的饱和LCFA棕榈酸对促性腺激素亚基基因的表达没有影响。此外,GW9508不影响启动子活性。接下来,我们检查了Fshb上游区域的缺失突变体,并发现Fshb上游调控区域(-2824至-2343 bp)是10μM不饱和LCFAs显著抑制作用的原因。我们的结果表明,Fshb的上游区域对不饱和LCFAs敏感。此外,不饱和LCFAs通过远端-2824至-2343 bp区域在抑制Fshb表达中发挥作用,这可能独立于LCFA受体GPR120途径。