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L-精氨酸通过激活GPRC6A/PI3K/AKT/mTOR信号通路刺激青春期小鼠乳腺上皮细胞的增殖和乳腺发育。

L-arginine stimulates the proliferation of mouse mammary epithelial cells and the development of mammary gland in pubertal mice by activating the GPRC6A/PI3K/AKT/mTOR signalling pathway.

作者信息

Ge Yusong, Li Feng, He Yuan, Cao Yu, Guo Wenjin, Hu Guiqiu, Liu Juxiong, Fu Shoupeng

机构信息

Department of Theoretic Veterinary Medicine, College of Veterinary Medicine, Jilin University, Changchun, Jilin, China.

出版信息

J Anim Physiol Anim Nutr (Berl). 2022 Nov;106(6):1383-1395. doi: 10.1111/jpn.13730. Epub 2022 May 26.

Abstract

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.

摘要

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。

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