首页> 美国卫生研究院文献>Molecules and Cells >Arginine Supplementation Recovered the IFN-γ-Mediated Decrease in Milk Protein and Fat Synthesis by Inhibiting the GCN2/eIF2α Pathway Which Induces Autophagy in Primary Bovine Mammary Epithelial Cells
【2h】

Arginine Supplementation Recovered the IFN-γ-Mediated Decrease in Milk Protein and Fat Synthesis by Inhibiting the GCN2/eIF2α Pathway Which Induces Autophagy in Primary Bovine Mammary Epithelial Cells

机译:补充精氨酸可通过抑制GCN2 /eIF2α途径(其诱导牛原代乳腺上皮细胞自噬)来恢复牛奶蛋白和脂肪合成中IFN-γ介导的减少。

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。
获取外文期刊封面目录资料

摘要

During the lactation cycle of the bovine mammary gland, autophagy is induced in bovine mammary epithelial cells (BMECs) as a cellular homeostasis and survival mechanism. Interferon gamma (IFN-γ) is an important antiproliferative and apoptogenic factor that has been shown to induce autophagy in multiple cell lines in vitro. However, it remains unclear whether IFN-γ can induce autophagy and whether autophagy affects milk synthesis in BMECs. To understand whether IFN-γ affects milk synthesis, we isolated and purified primary BMECs and investigated the effect of IFN-γ on milk synthesis in primary BMECs in vitro. The results showed that IFN-γ significantly inhibits milk synthesis and that autophagy was clearly induced in primary BMECs in vitro within 24 h. Interestingly, autophagy was observed following IFN-γ treatment, and the inhibition of autophagy can improve milk protein and milk fat synthesis. Conversely, upregulation of autophagy decreased milk synthesis. Furthermore, mechanistic analysis confirmed that IFN-γ mediated autophagy by depleting arginine and inhibiting the general control nonderepressible-2 kinase (GCN2)/eukaryotic initiation factor 2α (eIF2α) signaling pathway in BMECs. Then, it was found that arginine supplementation could attenuate IFN-γ-induced autophagy and recover milk synthesis to some extent. These findings may not only provide a novel measure for preventing the IFN-γ-induced decrease in milk quality but also a useful therapeutic approach for IFN-γ-associated breast diseases in other animals and humans.
机译:在牛乳腺的泌乳周期中,自噬在牛乳腺上皮细胞(BMEC)中被诱导为细胞稳态和存活机制。干扰素γ(IFN-γ)是重要的抗增殖和凋亡因子,已显示在体​​外能诱导多种细胞系自噬。但是,尚不清楚IFN-γ是否可以诱导自噬,以及自噬是否影响BMEC中的牛奶合成。为了了解IFN-γ是否影响牛奶的合成,我们分离和纯化了初级BMEC,并研究了IFN-γ对体外BMEC中牛奶合成的影响。结果表明,IFN-γ显着抑制乳汁的合成,并且在24小时内在体外BMEC中明显诱导了自噬。有趣的是,在IFN-γ处理后观察到自噬,并且抑制自噬可以改善乳蛋白和乳脂合成。相反,自噬的上调会降低牛奶的合成。此外,机制分析证实,IFN-γ通过消耗精氨酸并抑制BMEC中的一般控制非抑制性2激酶(GCN2)/真核起始因子2α(eIF2α)信号通路而介导的自噬。然后,发现精氨酸补充可以减弱IFN-γ诱导的自噬并在一定程度上恢复牛奶的合成。这些发现不仅可以提供预防IFN-γ引起的牛奶质量下降的新方法,而且可以为其他动物和人类中与IFN-γ相关的乳腺疾病提供有用的治疗方法。

著录项

相似文献

  • 外文文献
  • 中文文献
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号