Fine-tuning of AMPK–ULK1–mTORC1 regulatory triangle is crucial for autophagy oscillation

安普克 ULK1 mTORC1型 自噬 细胞生物学 激活剂(遗传学) 蛋白激酶A 激酶 化学 生物 信号转导 生物化学 PI3K/AKT/mTOR通路 受体 细胞凋亡
作者
Marianna Holczer,Bence Hajdú,Tamás Lőrincz,András Szarka,Gábor Bánhegyi,Orsolya Kapuy
出处
期刊:Scientific Reports [Springer Nature]
卷期号:10 (1) 被引量:45
标识
DOI:10.1038/s41598-020-75030-8
摘要

Abstract Autophagy is an intracellular digestive process, which has a crucial role in maintaining cellular homeostasis by self-eating the unnecessary and/or damaged components of the cell at various stress events. ULK1, one of the key elements of autophagy activator complex, together with the two sensors of nutrient and energy conditions, called mTORC1 and AMPK kinases, guarantee the precise function of cell response mechanism. We claim that the feedback loops of AMPK–mTORC1–ULK1 regulatory triangle determine an accurate dynamical characteristic of autophagic process upon cellular stress. By using both molecular and theoretical biological techniques, here we reveal that a delayed negative feedback loop between active AMPK and ULK1 is essential to manage a proper cellular answer after prolonged starvation or rapamycin addition. AMPK kinase quickly gets induced followed by AMPK-P-dependent ULK1 activation, whereas active ULK1 has a rapid negative effect on AMPK-P resulting in a delayed inhibition of ULK1. The AMPK-P → ULK1 ˧ AMPK-P negative feedback loop results in a periodic repeat of their activation and inactivation and an oscillatory activation of autophagy, as well. We demonstrate that the periodic induction of self-cannibalism is necessary for the proper dynamical behaviour of the control network when mTORC1 is inhibited with respect to various stress events. By computational simulations we also suggest various scenario to introduce “delay” on AMPK-P-dependent ULK1 activation (i.e. extra regulatory element in the wiring diagram or multi-phosphorylation of ULK1).

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
刚刚
香蕉觅云应助魏京京采纳,获得10
1秒前
Owen应助董晓萱采纳,获得10
1秒前
SciGPT应助奋斗的初阳采纳,获得10
1秒前
海关监管环境完成签到,获得积分20
1秒前
所所应助老迟到的可乐采纳,获得10
1秒前
awaw发布了新的文献求助10
1秒前
fxx发布了新的文献求助10
1秒前
charint应助热心的雁桃采纳,获得20
2秒前
2秒前
感动的煜城完成签到,获得积分10
2秒前
挚友发布了新的文献求助10
2秒前
zhangzhen完成签到,获得积分10
2秒前
2秒前
4512完成签到,获得积分10
2秒前
2秒前
2秒前
小草莓完成签到,获得积分20
3秒前
lee完成签到,获得积分10
3秒前
回答完成签到,获得积分20
3秒前
wangshibing发布了新的文献求助10
3秒前
4秒前
科研通AI6.3应助勇yi采纳,获得10
4秒前
qiuling发布了新的文献求助200
5秒前
5秒前
研友_VZG7GZ应助砍柴少年采纳,获得10
5秒前
热心市民小红花应助shulan采纳,获得30
5秒前
科研通AI6.3应助苏su采纳,获得10
5秒前
Hello应助清脆的水蜜桃采纳,获得10
5秒前
公冶灵安完成签到,获得积分10
5秒前
善学以致用应助靓靓靓采纳,获得10
6秒前
诺曼发布了新的文献求助10
6秒前
举个栗子完成签到,获得积分20
6秒前
lin发布了新的文献求助10
6秒前
豪豪完成签到,获得积分10
6秒前
上官若男应助wan采纳,获得10
6秒前
cssfsa发布了新的文献求助10
6秒前
7秒前
7秒前
感动的海露完成签到 ,获得积分10
7秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Kinesiophobia : a new view of chronic pain behavior 5000
Molecular Biology of Cancer: Mechanisms, Targets, and Therapeutics 3000
First commercial application of ELCRES™ HTV150A film in Nichicon capacitors for AC-DC inverters: SABIC at PCIM Europe 1000
Handbook of pharmaceutical excipients, Ninth edition 800
Signals, Systems, and Signal Processing 610
Digital and Social Media Marketing 600
热门求助领域 (近24小时)
化学 医学 生物 材料科学 工程类 有机化学 内科学 生物化学 物理 计算机科学 纳米技术 遗传学 基因 复合材料 化学工程 物理化学 病理 催化作用 免疫学 量子力学
热门帖子
关注 科研通微信公众号,转发送积分 5992205
求助须知:如何正确求助?哪些是违规求助? 7441952
关于积分的说明 16065006
捐赠科研通 5134084
什么是DOI,文献DOI怎么找? 2753763
邀请新用户注册赠送积分活动 1726606
关于科研通互助平台的介绍 1628468