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hvps34, an ancient player, enters a growing game: mTOR Complex1/S6K1 signaling.

机译:hvps34,一个古老的玩家,正在进入一个不断发展的游戏:mTOR Complex1 / S6K1信号。

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摘要

Recent studies have shown that the nutrient input to the mTOR Complex1/S6K1 signaling pathway is mediated by class 3 PI3K or hVps34, the oldest member of the PI3K family. Moreover, studies to date would suggest that during the evolution of multicellular organisms this ancient branch of the pathway was merged with the growth-factor-hormone-controlled class 1 PI3K pathway at the level of mTOR Complex1 to control the development and growth of the organism. However, hVps34 also plays a role in the regulation of macroautophagy - the mechanism by which cells generate nutrients, such as amino acids, through the degradation of intracellular complexes, including mitochondria and ribosomes. These functions of hVps34 initially appear contradictory, since increased mTOR Complex1 activation is triggered by increased amino acid levels, while autophagy is triggered when cells are faced with amino acid deprivation.
机译:最近的研究表明,mTOR Complex1 / S6K1信号途径的营养输入是由PI3K家族中最老的3类PI3K或hVps34介导的。此外,迄今为止的研究表明,在多细胞生物的进化过程中,该途径的这一古老分支在mTOR Complex1的水平与生长因子激素控制的1类PI3K途径融合,以控制该生物的生长。但是,hVps34在调控巨噬细胞自噬中也发挥着作用-这种机制是细胞通过降解包括线粒体和核糖体在内的细胞内复合物而产生营养物质(例如氨基酸)的机制。 hVps34的这些功能最初似乎是矛盾的,因为增加的氨基酸水平会触发增加的mTOR Complex1激活,而当细胞面临氨基酸剥夺时会触发自噬。

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