CaMKIIβ Ca2+ptures ER signals to initiate autophagosome biogenesis

IF 16.6 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY Molecular Cell Pub Date : 2025-02-06 DOI:10.1016/j.molcel.2025.01.011
Leonardo Luís Artico, Ana Paula Arruda
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引用次数: 0

Abstract

Cytosolic Ca2+ transients are critical signals for autophagy regulation; however, how they translate into functional autophagic events remains unclear. In this issue of Molecular Cell, Zheng et al.1 identify CaMKIIβ as a key player decoding Ca2+ transients at the ER surface to initiate autophagosome formation through the FIP200 complex.
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CaMKIIβ Ca2+诱导 ER 信号启动自噬体生物生成
胞质Ca2+瞬态是自噬调节的关键信号;然而,它们如何转化为功能性自噬事件仍不清楚。在这一期的Molecular Cell中,Zheng等人1发现CaMKIIβ是解码内质网表面Ca2+瞬态的关键参与者,通过FIP200复合体启动自噬体的形成。
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来源期刊
Molecular Cell
Molecular Cell 生物-生化与分子生物学
CiteScore
26.00
自引率
3.80%
发文量
389
审稿时长
1 months
期刊介绍: Molecular Cell is a companion to Cell, the leading journal of biology and the highest-impact journal in the world. Launched in December 1997 and published monthly. Molecular Cell is dedicated to publishing cutting-edge research in molecular biology, focusing on fundamental cellular processes. The journal encompasses a wide range of topics, including DNA replication, recombination, and repair; Chromatin biology and genome organization; Transcription; RNA processing and decay; Non-coding RNA function; Translation; Protein folding, modification, and quality control; Signal transduction pathways; Cell cycle and checkpoints; Cell death; Autophagy; Metabolism.
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