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

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.

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Publication Details

Journal
Molecular Biology of the Cell
Published
2024-12-04
DOI
https://doi.org/10.1091/mbc.e24-04-0197
Citations
2
Primary Topic
Cellular transport and secretion
Type
article
Field-Weighted Citation Impact
0.65

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article

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

John Salogiannis, Allison Langley, Sarah Abeling-Wang, Erinn Wagner
2 citations
Molecular Biology of the Cell
Cellular transport and secretion
0.65
article

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

John Salogiannis, Allison Langley, Sarah Abeling-Wang, Erinn Wagner
article en
2 citations

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.

Molecular Biology of the CellVol. 36(1)
University of Vermont (US)
National Institutes of Health, National Institute of General Medical Sciences
Openalex Percentile: Top 31%
Cellular transport and secretion
0.65
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Movement of the endoplasmic reticulum is driven by multiple classes of vesicles marked by Rab-GTPases — John Salogiannis, Allison Langley, et al. · Molecular Biology of the Cell (2024) | TGRS Research Map | TGRS