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内质网的移动由以Rab-GTP酶为标记的多种囊泡驱动。

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

作者信息

Langley Allison, Abeling-Wang Sarah, Wagner Erinn, Salogiannis John

机构信息

Cellular, Molecular, and Biomedical Sciences Graduate Program, University of Vermont, Burlington, VT 05405.

Department of Molecular Physiology and Biophysics, Larner College of Medicine at the University of Vermont, Burlington, VT 05405.

出版信息

Mol Biol Cell. 2025 Jan 1;36(1):ar9. doi: 10.1091/mbc.E24-04-0197. Epub 2024 Dec 4.

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.

摘要

外周内质网(ER)小管沿着微管移动,通过膜接触位点与各种细胞器相互作用。传统上,内质网的移动方式要么是通过分子马达沿着稳定的微管滑动,要么是通过末端附着复合物(TAC)附着在动态微管的正端。最近发现的第三种方式——搭便车,涉及到运动性囊泡沿着微管拉动内质网小管。先前的研究表明,内质网搭Rab5和Rab7标记的内体的便车,但尚不确定其他Rab囊泡是否也能如此。在U2OS细胞中,我们筛选了Rabs与内质网小管共运输的能力,发现内质网搭Rab6(异构体a和b)标记的高尔基体后囊泡的便车。Rab6介导的内质网搭便车独立于内质网-内溶酶体接触和TAC介导的内质网移动。耗尽Rab6以及Rab6囊泡的运动性会降低内质网的整体移动。相反,将这些囊泡重新定位到细胞周边会导致外周内质网积累,这表明Rab6囊泡的运动性对于内质网的一部分移动至关重要。由TGN46标记的近端高尔基体后囊泡参与Rab6介导的内质网搭便车,而晚期高尔基体囊泡(Rabs 8/10/11/13/14)对于内质网移动并非必不可少。我们的进一步分析发现,由Rab1标记的内质网到高尔基体囊泡也能够驱动内质网的一部分移动。综上所述,我们的研究结果表明,内质网搭Rab囊泡的便车是内质网移动的一种重要方式。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b5c0/11742117/2602f180e00a/mbc-36-ar9-g001.jpg

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