Evidence map›Paper›PMID 33554435›Full record

ArticleEMBO reports2021

Mobile late endosomes modulate peripheral endoplasmic reticulum network architecture.

Menno Spits, Iris T Heesterbeek, Lennard M Voortman, Jimmy J Akkermans, Ruud H Wijdeven, Birol Cabukusta, Jacques Neefjes

Open access · greenAbstract read
In one paragraph

Article in EMBO reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 1 pooled it
5.1field-weighted citation impact, top 3% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

20 citing papers in PubMed, 1 synthesis or guideline pooled it, 54 citations in OpenAlex.

  1. Stay in touch with the endoplasmic reticulum.Science China. Life sciences · 2024
    Pooled it
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  20. Membrane Contact Sites in Proteostasis and ER Stress Response.Contact (Thousand Oaks (Ventura County, Calif.))
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 1 institution in 1 country.

Menno SpitsDivision of Cell and Chemical Biology, Oncode Institute, Leiden University Medical Centre, Leiden, The Netherlands.
Iris T HeesterbeekDivision of Cell and Chemical Biology, Oncode Institute, Leiden University Medical Centre, Leiden, The Netherlands.
Lennard M VoortmanDivision of Cell and Chemical Biology, Oncode Institute, Leiden University Medical Centre, Leiden, The Netherlands.
Jimmy J AkkermansDivision of Cell and Chemical Biology, Oncode Institute, Leiden University Medical Centre, Leiden, The Netherlands.
Ruud H WijdevenDivision of Cell and Chemical Biology, Oncode Institute, Leiden University Medical Centre, Leiden, The Netherlands.
Birol CabukustaDivision of Cell and Chemical Biology, Oncode Institute, Leiden University Medical Centre, Leiden, The Netherlands.ORCID 0000-0002-1187-3048
Jacques NeefjesDivision of Cell and Chemical Biology, Oncode Institute, Leiden University Medical Centre, Leiden, The Netherlands.ORCID 0000-0001-6763-2211
Leiden University · NL

Funding

European Research Council ERC-2015-AdG
6 · The paper itself

Abstract

The endoplasmic reticulum (ER) is the largest organelle contacting virtually every other organelle for information exchange and control of processes such as transport, fusion, and fission. Here, we studied the role of the other organelles on ER network architecture in the cell periphery. We show that the co-migration of the ER with other organelles, called ER hitchhiking facilitated by late endosomes and lysosomes is a major mechanism controlling ER network architecture. When hitchhiking occurs, emerging ER structures may fuse with the existing ER tubules to alter the local ER architecture. This couples late endosomal/lysosomal positioning and mobility to ER network architecture. Conditions restricting late endosomal movement-including cell starvation-or the depletion of tether proteins that link the ER to late endosomes reduce ER dynamics and limit the complexity of the peripheral ER network architecture. This indicates that among many factors, the ER is controlled by late endosomal movement resulting in an alteration of the ER network architecture.

Indexed as

Endoplasmic ReticulumEndosomesBiological TransportLysosomesendoplasmic reticulumlate endosomesmembrane contact sitesorganelle hitchhikingstarvation

Identifiers

PMID33554435
PMCPMC7926257
OpenAlexW3128170839

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.