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首页> 外文期刊>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
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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(在原代牛乳腺上皮细胞中诱导自噬)恢复牛奶蛋白和脂肪合成中IFN-γ介导的减少。

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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,在牛乳腺上皮细胞(BMEC)中自噬被诱导为细胞稳态和存活机制。干扰素γ(IFN-γ)是一种重要的抗增殖和凋亡因子,已被证明可在多种细胞系中诱导自噬。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,我们分离纯化了原代BMECs,并研究了IFN-γ对原代BMECs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 h内体外明显诱导了原代BMEC的自噬。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,机理分析证实,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措施,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。

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