Ge Yusong, Li Feng, He Yuan, Cao Yu, Guo Wenjin, Hu Guiqiu, Liu Juxiong, Fu Shoupeng
Department of Theoretic Veterinary Medicine, College of Veterinary Medicine, Jilin University, Changchun, Jilin, China.
J Anim Physiol Anim Nutr (Berl). 2022 Nov;106(6):1383-1395. doi: 10.1111/jpn.13730. Epub 2022 May 26.
Amino acids have been shown to affect the development of mammary gland (MG). However, it is unclear whether L-arginine promotes the development of pubertal MG. Therefore, our study aims to explore the effect of L-arginine on the development of MG in pubertal mice. To investigate its internal mechanism of action, we will use mouse mammary epithelial cells (mMECs) line. Whole-mount staining showed that L-arginine can promote the extension of MG duct. In vitro, 0.4 mM L-arginine could activate the G protein-coupled receptor family C, group 6, subtype A (GPRC6A)/phosphoinositide 3-kinase (PI3K)/protein kinase B (AKT)/mammalian target of rapamycin (mTOR) signalling pathway and increase the phosphorylation of eukaryotic initiation factor 4E binding protein 1 (4EBP1) to promote the synthesis of cell cycle regulatory protein D1 (Cyclin D1), leading to the dissociation of the retinoblastoma tumour suppressor protein (Rb)-E2F1 transcription factor (E2F1) complex in mMECs and releasing E2F1 to promote cell proliferation. Furthermore, GPRC6A was knocked down or inhibition of the PI3K/AKT/mTOR signalling pathway with corresponding inhibitors completely abolished the arginine-induced promotion of mMECs proliferation. In vivo, it was further confirmed that 0.1% L-arginine can activate the PI3K/AKT/mTOR signalling pathway in the MG of pubertal mice. These results were able to indicate that L-arginine stimulates the development of MG in pubertal mice through the GPRC6A/PI3K/AKT/mTOR signalling pathway.
氨基酸已被证明会影响乳腺(MG)的发育。然而,尚不清楚L-精氨酸是否能促进青春期乳腺的发育。因此,我们的研究旨在探讨L-精氨酸对青春期小鼠乳腺发育的影响。为了研究其内在作用机制,我们将使用小鼠乳腺上皮细胞(mMECs)系。整装染色显示L-精氨酸可促进乳腺导管的延伸。在体外,0.4 mM L-精氨酸可激活G蛋白偶联受体家族C第6组成员A(GPRC6A)/磷脂酰肌醇3-激酶(PI3K)/蛋白激酶B(AKT)/雷帕霉素哺乳动物靶蛋白(mTOR)信号通路,并增加真核起始因子4E结合蛋白1(4EBP1)的磷酸化,以促进细胞周期调节蛋白D1(Cyclin D1)的合成,导致视网膜母细胞瘤肿瘤抑制蛋白(Rb)-E2F1转录因子(E2F1)复合物在mMECs中解离并释放E2F1以促进细胞增殖。此外,敲低GPRC6A或用相应抑制剂抑制PI3K/AKT/mTOR信号通路可完全消除精氨酸诱导的mMECs增殖促进作用。在体内,进一步证实0.1% L-精氨酸可激活青春期小鼠乳腺中的PI3K/AKT/mTOR信号通路。这些结果表明,L-精氨酸通过GPRC6A/PI3K/AKT/mTOR信号通路刺激青春期小鼠乳腺的发育。