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振荡性自噬诱导是由更新的AMPK-ULK1调节通路实现的。

Oscillatory autophagy induction is enabled by an updated AMPK-ULK1 regulatory wiring.

作者信息

Kapuy Orsolya, Holczer Marianna, Csabai Luca, Korcsmáros Tamás

机构信息

Department of Molecular Biology, Institute of Biochemistry and Molecular Biology, Semmelweis University, Budapest, Hungary.

Department of Genetics, ELTE Eötvös Loránd University, Budapest, Hungary.

出版信息

PLoS One. 2024 Dec 26;19(12):e0313302. doi: 10.1371/journal.pone.0313302. eCollection 2024.

Abstract

Autophagy-dependent survival relies on a crucial oscillatory response during cellular stress. Although oscillatory behaviour is typically associated with processes like the cell cycle or circadian rhythm, emerging experimental and theoretical evidence suggests that such periodic dynamics may explain conflicting experimental results in autophagy research. In this study, we demonstrate that oscillatory behaviour in the regulation of the non-selective, stress-induced macroautophagy arises from a series of interlinked negative and positive feedback loops within the mTORC1-AMPK-ULK1 regulatory triangle. While many of these interactions have been known for decades, recent discoveries have revealed how mTORC1, AMPK, and ULK1 are truly interconnected. Although these new findings initially appeared contradictory to established models, additional experiments and our systems biology analysis clarify the updated regulatory structure. Through computational modelling of the autophagy oscillatory response, we show how this regulatory network governs autophagy induction. Our results not only reconcile previous conflicting experimental observations but also offer insights for refining autophagy regulation and advancing understanding of its mechanisms of action.

摘要

自噬依赖性存活依赖于细胞应激期间关键的振荡反应。尽管振荡行为通常与细胞周期或昼夜节律等过程相关,但新出现的实验和理论证据表明,这种周期性动态可能解释自噬研究中相互矛盾的实验结果。在本研究中,我们证明非选择性、应激诱导的巨自噬调节中的振荡行为源于mTORC1-AMPK-ULK1调节三角内一系列相互关联的负反馈和正反馈回路。虽然其中许多相互作用已为人所知数十年,但最近的发现揭示了mTORC1、AMPK和ULK1是如何真正相互连接的。尽管这些新发现最初似乎与既定模型相矛盾,但额外的实验和我们的系统生物学分析阐明了更新后的调节结构。通过对自噬振荡反应的计算建模,我们展示了这个调节网络如何控制自噬诱导。我们的结果不仅调和了先前相互矛盾的实验观察结果,还为完善自噬调节和推进对其作用机制的理解提供了见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b237/11671020/f3ff7977e3ed/pone.0313302.g001.jpg

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