mTOR复合物之间的信号串扰

Jianling Xie, C. Proud
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引用次数: 52

摘要

mTOR是一种蛋白激酶,它整合了多种环境和细胞内刺激,积极调节细胞的许多合成代谢过程,包括蛋白质合成。它存在于两个高度保守的多蛋白复合物mTORC1和2mtorc2中。这些复合物磷酸化不同的下游靶点,并在不同的细胞功能中发挥作用。它们还对mTOR抑制剂雷帕霉素表现出独特的敏感性。然而,尽管它们的生化和功能不同,最近的研究表明,这些复合物的调节是紧密相连的。例如,mTORC1和2都有一些共同的上游信号分子,如PI3K和结节硬化复合体TSC,这些分子控制着它们的激活。对mTOR复合物的刺激也可能触发正反馈和负反馈机制,然后反过来进一步增强或抑制它们的激活。在这里,我们总结了一些最近发现的与mTORC1和mtor2之间串扰有关的特征。然后,我们讨论了异常mTOR复合物串扰机制如何影响人类疾病和耐药性的发展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Signaling crosstalk between the mTOR complexes
mTOR is a protein kinase which integrates a variety of environmental and intracellular stimuli to positively regulate many anabolic processes of the cell, including protein synthesis. It exists within two highly conserved multi-protein complexes known as mTORC1 and 2 mTORC2. Each of these complexes phosphorylates different downstream targets, and play roles in different cellular functions. They also show distinctive sensitivity to the mTOR inhibitor rapamycin. Nevertheless, despite their biochemical and functional differences, recent studies have suggested that the regulation of these complexes is tightly linked to each other. For instance, both mTORC1 and 2 share some common upstream signaling molecules, such as PI3K and tuberous sclerosis complex TSC, which control their activation. Stimulation of the mTOR complexes may also trigger both positive and negative feedback mechanisms, which then in turn either further enhance or suppress their activation. Here, we summarize some recently discovered features relating to the crosstalk between mTORC1 and 2. We then discuss how aberrant mTOR complex crosstalk mechanisms may have an impact on the development of human diseases and drug resistance.
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