Meng Yingying, Yuan Cong, Zhang Jing, Zhang Fenglin, Fu Qin, Zhu Xiaotong, Shu Gang, Wang Lina, Gao Ping, Xi Qianyun, Sun Jiajie, Zhang Yongliang, Jiang Qingyan, Wang Songbo
Guangdong Provincial Key Laboratory of Animal Nutrition Control, College of Animal Science, South China Agricultural University, Guangzhou 510642, PR China; National Engineering Research Center for Breeding Swine Industry, South China Agricultural University, Guangzhou 510642, PR China.
Guangdong Provincial Key Laboratory of Animal Nutrition Control, College of Animal Science, South China Agricultural University, Guangzhou 510642, PR China; National Engineering Research Center for Breeding Swine Industry, South China Agricultural University, Guangzhou 510642, PR China.
Biochem Biophys Res Commun. 2017 Sep 9;491(1):192-197. doi: 10.1016/j.bbrc.2017.07.075. Epub 2017 Jul 13.
It has been demonstrated that dietary high fat diet negatively affects the pubertal mammary gland development. The aim of the present study was to investigate the effects of stearic acid (SA), an 18-carbon chain saturated fatty acid, on mammary gland development in pubertal mice and to explore the underlying mechanism. Our results demonstrated that dietary supplementation of 2% SA suppressed mammary duct development, with significant reduction of terminal end bud (TEB) number and ductal branch. In accord, the expression of proliferative marker Cyclin D1 was markedly decreased by dietary SA. Furthermore, dietary SA led to increase of G protein-coupled receptor 120 (GPR120) expression and inhibition of PI3K/Akt signaling pathway in mammary gland of pubertal mice. In good agreement with the in vivo findings, the in vitro results showed that 40 μM SA significantly suppressed proliferation of mouse mammary epithelial cell HC11 by regulating mRNA and/or protein expression of proliferative markers such as Cyclin D1/3, p21, and PCNA. Meanwhile, SA activated GPR120 and inhibited PI3K/Akt signaling pathway in a GPR120-dependent manner. In addition, SA-induced inhibition of PI3K/Akt signaling pathway, suppression of HC11 proliferation, and alteration of proliferative markers expression were abolished by knockdown of GPR120 with siRNA. Collectively, these findings showed that SA suppressed mammary gland development of pubertal mice, which was coincident with the SA-inhibited HC11 proliferation, and was associated with inhibition of PI3K/Akt signaling pathway through activation of GPR120. These data provided new insights into the regulation of mammary gland development by dietary fatty acids.
已证明饮食中的高脂肪饮食会对青春期乳腺发育产生负面影响。本研究的目的是调查硬脂酸(SA)(一种18碳链饱和脂肪酸)对青春期小鼠乳腺发育的影响,并探索其潜在机制。我们的结果表明,饮食中补充2%的SA会抑制乳腺导管发育,终末芽(TEB)数量和导管分支显著减少。与此一致,饮食中的SA使增殖标志物细胞周期蛋白D1的表达明显降低。此外,饮食中的SA导致青春期小鼠乳腺中G蛋白偶联受体120(GPR120)表达增加,并抑制PI3K/Akt信号通路。与体内研究结果高度一致,体外研究结果表明,40μM的SA通过调节细胞周期蛋白D1/3、p21和增殖细胞核抗原(PCNA)等增殖标志物的mRNA和/或蛋白质表达,显著抑制小鼠乳腺上皮细胞HC11的增殖。同时,SA以GPR120依赖的方式激活GPR120并抑制PI3K/Akt信号通路。此外,用小干扰RNA(siRNA)敲低GPR120可消除SA诱导的PI3K/Akt信号通路抑制、HC11增殖抑制以及增殖标志物表达的改变。总的来说,这些发现表明SA抑制青春期小鼠的乳腺发育,这与SA抑制HC11增殖一致,并且与通过激活GPR120抑制PI3K/Akt信号通路有关。这些数据为饮食脂肪酸对乳腺发育的调节提供了新的见解。