破坏 AMBRA1 和 DLC1 之间的相互作用可防止细胞凋亡,同时增强自噬和有丝分裂。

IF 1.8 4区 生物学 Q3 BIOLOGY
Biology Open Pub Date : 2024-12-15 Epub Date: 2024-11-26 DOI:10.1242/bio.060380
Kate Hawkins, Meg Watt, Sébastien Gillotin, Maya Hanspal, Martin Helley, Jill Richardson, Nicola Corbett, Janet Brownlees
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引用次数: 0

摘要

AMBRA1 在自噬、有丝分裂、细胞周期调控、神经发生和细胞凋亡中发挥着关键作用。这些过程的失调是各种神经退行性疾病的特征,因此 AMBRA1 是一个潜在的治疗靶点。AMBRA1 固有无序区的灵活性使其能够发生构象变化,从而发挥其作为各种不同复合物的适配蛋白的功能。了解这些多重蛋白-蛋白相互作用的相关性将使我们能够获得有关哪些蛋白可以作为药理靶点的信息。为了比较潜在的 AMBRA1 激活策略,我们设计并验证了几种以前描述过的突变构建物,并鉴定了它们对 SHSY5Y 细胞的增殖、凋亡、自噬和有丝分裂的影响。AMBRA1TAT是AMBRA1的一种突变形式,它不能与微管上的DLC1相互作用。过量表达这种突变体可保护细胞免受凋亡,并诱导 SHSY5Y 细胞的自噬/半自噬,此外还能增强小鼠 NSCs 从静止到增殖的转换。未来的研究应侧重于设计能抑制AMBRA1/DLC1之间蛋白-蛋白相互作用的化合物,从而有可能将其用作治疗神经退行性变的药物策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Disrupting the interaction between AMBRA1 and DLC1 prevents apoptosis while enhancing autophagy and mitophagy.

AMBRA1 has critical roles in autophagy, mitophagy, cell cycle regulation, neurogenesis and apoptosis. Dysregulation of these processes are hallmarks of various neurodegenerative diseases and therefore AMBRA1 represents a potential therapeutic target. The flexibility of its intrinsically disordered regions allows AMBRA1 to undergo conformational changes and thus to perform its function as an adaptor protein for various different complexes. Understanding the relevance of these multiple protein-protein interactions will allow us to gain information about which to target pharmacologically. To compare potential AMBRA1 activation strategies, we have designed and validated several previously described mutant constructs in addition to characterising their effects on proliferation, apoptosis, autophagy and mitophagy in SHSY5Y cells. AMBRA1TAT, which is a mutant form of AMBRA1 that cannot interact with DLC1 at the microtubules, produced the most promising results. Overexpression of this mutant protected cells against apoptosis and induced autophagy/mitophagy in SHSY5Y cells in addition to enhancing the switch from quiescence to proliferation in mouse neural stem cells. Future studies should focus on designing compounds that inhibit the protein-protein interaction between AMBRA1/DLC1 and thus have potential to be used as a drug strategy for neurodegeneration.

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来源期刊
Biology Open
Biology Open BIOLOGY-
CiteScore
3.90
自引率
0.00%
发文量
162
审稿时长
8 weeks
期刊介绍: Biology Open (BiO) is an online Open Access journal that publishes peer-reviewed original research across all aspects of the biological sciences. BiO aims to provide rapid publication for scientifically sound observations and valid conclusions, without a requirement for perceived impact.
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