Movement of the endoplasmic reticulum is driven by multiple classes of vesicles marked by Rab-GTPases.

IF 3.1 3区 生物学 Q3 CELL BIOLOGY
Molecular Biology of the Cell Pub Date : 2025-01-01 Epub Date: 2024-12-04 DOI:10.1091/mbc.E24-04-0197
Allison Langley, Sarah Abeling-Wang, Erinn Wagner, John Salogiannis
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引用次数: 0

Abstract

Peripheral endoplasmic reticulum (ER) tubules move along microtubules to interact with various organelles through membrane contact sites. Traditionally, ER moves by either sliding along stable microtubules via molecular motors or attaching to the plus ends of dynamic microtubules through tip attachment complexes (TAC). A recently discovered third process, hitchhiking, involves motile vesicles pulling ER tubules along microtubules. Previous research showed that ER hitchhikes on Rab5- and Rab7-marked endosomes, but it is uncertain whether other Rab-vesicles can do the same. In U2OS cells, we screened Rabs for their ability to cotransport with ER tubules and found that ER hitchhikes on post-Golgi vesicles marked by Rab6 (isoforms a and b). Rab6-ER hitchhiking occurs independently of ER-endolysosome contacts and TAC-mediated ER movement. Depleting Rab6 and the motility of Rab6-vesicles reduces overall ER movement. Conversely, relocating these vesicles to the cell periphery causes peripheral ER accumulation, indicating that Rab6-vesicle motility is crucial for a subset of ER movements. Proximal post-Golgi vesicles marked by TGN46 are involved in Rab6-ER hitchhiking, while late Golgi vesicles (Rabs 8/10/11/13/14) are not essential for ER movement. Our further analysis finds that ER to Golgi vesicles marked by Rab1 are also capable of driving a subset of ER movements. Taken together, our findings suggest that ER hitchhiking on Rab-vesicles is a significant mode of ER movement.

内质网的运动是由多类以Rab-GTPases为标志的囊泡驱动的。
外周内质网(ER)小管沿着微管移动,通过膜接触点(MCS)与各种细胞器相互作用。传统上,内质网通过分子马达沿着稳定的微管滑动或通过尖端附着复合物(TAC)附着在动态微管的正端来移动。最近发现的第三种过程,搭便车,涉及到移动的囊泡沿着微管牵引内质网小管。先前的研究表明,ER在Rab5-和rab7标记的核内体上搭便车,但不确定其他Rab5-囊泡是否也能做到这一点。在U2OS细胞中,我们筛选了Rab6与ER小管共同运输的能力,发现ER在以Rab6为标记的高尔基囊泡上搭便车(a和b亚型)。Rab6-ER搭便车的发生独立于ER内溶酶体接触和tac介导的ER运动。Rab6的消耗和Rab6囊泡的运动减少了内质网的整体运动。相反,将这些囊泡迁移到细胞外周会导致外周内质网积聚,这表明rab6囊泡的运动对内质网运动的一个子集至关重要。以TGN46标记的近端高尔基后囊泡参与Rab6-ER的搭便车,而晚期高尔基囊泡(Rabs 8/10/11/13/14)对ER的移动并不重要。我们进一步的分析发现,Rab1标记的ER到高尔基囊泡也能够驱动ER的一部分运动。综上所述,我们的研究结果表明,ER搭乘rab -囊泡是ER运动的一种重要模式。[媒体:见文本][媒体:见文本][媒体:见文本][媒体:见文本][媒体:见文本][媒体:见文本][媒体:见文本][媒体:见文本][媒体:见文本]。
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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来源期刊
Molecular Biology of the Cell
Molecular Biology of the Cell 生物-细胞生物学
CiteScore
6.00
自引率
6.10%
发文量
402
审稿时长
2 months
期刊介绍: MBoC publishes research articles that present conceptual advances of broad interest and significance within all areas of cell, molecular, and developmental biology. We welcome manuscripts that describe advances with applications across topics including but not limited to: cell growth and division; nuclear and cytoskeletal processes; membrane trafficking and autophagy; organelle biology; quantitative cell biology; physical cell biology and mechanobiology; cell signaling; stem cell biology and development; cancer biology; cellular immunology and microbial pathogenesis; cellular neurobiology; prokaryotic cell biology; and cell biology of disease.
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