The mammalian actin elongation factor ENAH/MENA contributes to autophagosome formation via its actin regulatory function.

Autophagy Pub Date : 2024-08-01 Epub Date: 2024-06-11 DOI:10.1080/15548627.2024.2347105
Yueheng Li, Yafei Zhang, Menghui Wang, Junhui Su, Xinjue Dong, Yuqi Yang, Hongshan Wang, QingQuan Li
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Abstract

Macroautophagy/autophagy is a catabolic process crucial for degrading cytosolic components and damaged organelles to maintain cellular homeostasis, enabling cells to survive in extreme extracellular environments. ENAH/MENA, a member of the Ena/VASP protein family, functions as a highly efficient actin elongation factor. In this study, our objective was to explore the role of ENAH in the autophagy process. Initially, we demonstrated that depleting ENAH in cancer cells inhibits autophagosome formation. Subsequently, we observed ENAH's colocalization with MAP1LC3/LC3 during tumor cell starvation, dependent on actin cytoskeleton polymerization and the interaction between ENAH and BECN1 (beclin 1). Additionally, mammalian ATG9A formed a ring-like structure around ENAH-LC3 puncta during starvation, relying on actin cytoskeleton polymerization. Furthermore, ENAH's EVH1 and EVH2 domains were found to be indispensable for its colocalization with LC3 and BECN1, while the PRD domain played a crucial role in the formation of the ATG9A ring. Finally, our study revealed ENAH-led actin comet tails in autophagosome trafficking. In conclusion, our findings provide initial insights into the regulatory role of the mammalian actin elongation factor ENAH in autophagy.Abbreviations: 3-MA 3-methyladenine; ABPs actin-binding proteins; ATG autophagy related; ATG9A autophagy related 9A; Baf A1 bafilomycin A1; CM complete medium; CytERM endoplasmic reticulum signal-anchor membrane protein; Cyto D cytochalasin D; EBSS Earl's balanced salt solution; ENAH/MENA ENAH actin regulator; EVH1 Ena/VASP homology 1 domain; EVH2 Ena/VASP homology 2 domain; GAPDH glyceraldehyde-3-phosphate dehydrogenase; Lat B latrunculin B; LC3-I unlipidated form of LC3; LC3-II phosphatidylethanolamine-conjugated form of LC3; MAP1LC3/LC3 microtubule associated protein 1 light chain 3; mEGFP monomeric enhanced green fluorescent protein; mTagBFP2 monomeric Tag blue fluorescent protein 2; OSER organized smooth endoplasmic reticulum; PRD proline-rich domain; PtdIns3K class III phosphatidylinositol 3-kinase; WM wortmannin.

哺乳动物肌动蛋白伸长因子ENAH/MENA通过其肌动蛋白调节功能促进自噬体的形成。
大自噬/自噬是一种分解代谢过程,对降解细胞膜成分和受损细胞器以维持细胞稳态至关重要,可使细胞在极端的细胞外环境中存活。ENAH/MENA是ENA/VASP蛋白家族的成员,是一种高效的肌动蛋白伸长因子。在本研究中,我们的目标是探索ENAH在自噬过程中的作用。最初,我们证明了在癌细胞中消耗ENAH会抑制自噬体的形成。随后,我们观察到ENAH在肿瘤细胞饥饿过程中与MAP1LC3/LC3共定位,这依赖于肌动蛋白细胞骨架聚合以及ENAH与BECN1(beclin 1)之间的相互作用。此外,哺乳动物的 ATG9A 在饥饿过程中依靠肌动蛋白细胞骨架聚合在ENAH-LC3 点周围形成环状结构。此外,研究还发现ENAH的EVH1和EVH2结构域对于其与LC3和BECN1的共定位是不可或缺的,而PRD结构域则在ATG9A环的形成中起着关键作用。最后,我们的研究揭示了ENAH引导的肌动蛋白彗尾在自噬体迁移中的作用。总之,我们的研究结果为哺乳动物肌动蛋白伸长因子ENAH在自噬中的调控作用提供了初步见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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