Guo Zhixin, Wang Yanfeng, Feng Xue, Bao Chaogetu, He Qiburi, Bao Lili, Hao Huifang, Wang Zhigang
College of Life Science, Inner Mongolia University, Hohhot 010021, China.
College of Basic Medical Science, Inner Mongolia Medical University, Hohhot 010110, China.
Asian-Australas J Anim Sci. 2016 Nov;29(11):1646-1652. doi: 10.5713/ajas.15.0660. Epub 2016 Jan 18.
Mammalian target of rapamycin complex 1 (mTORC1) is a central regulator of cell growth and metabolism and is sufficient to induce specific metabolic processes, including lipid biosynthesis. Elongation of very-long-chain fatty acids 1 () is a ubiquitously expressed gene and the product of which was thought to be associated with elongation of carbon (C) chain in fatty acids. In the present study, we examined the effects of rapamycin, a specific inhibitor of mTORC1, on ELOVL1 expression and docosahexaenoic acid (DHA, C22:6 n-3) synthesis in bovine mammary epithelial cells (BMECs). We found that rapamycin decreased the relative abundance of mRNA, ELOVL1 expression and the level of DHA in a time-dependent manner. These data indicate that ELOVL1 expression and DHA synthesis are regulated by mTORC1 in BMECs.
雷帕霉素靶蛋白复合物1(mTORC1)是细胞生长和代谢的核心调节因子,足以诱导包括脂质生物合成在内的特定代谢过程。超长链脂肪酸延伸蛋白1(ELOVL1)是一个广泛表达的基因,其产物被认为与脂肪酸中碳(C)链的延伸有关。在本研究中,我们检测了mTORC1的特异性抑制剂雷帕霉素对牛乳腺上皮细胞(BMECs)中ELOVL1表达及二十二碳六烯酸(DHA,C22:6 n-3)合成的影响。我们发现雷帕霉素能以时间依赖性方式降低ELOVL1 mRNA的相对丰度、ELOVL1表达及DHA水平。这些数据表明,在BMECs中,ELOVL1表达和DHA合成受mTORC1调控。