Evidence map›Paper›PMID 35377783›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2022

A role for endoplasmic reticulum dynamics in the cellular distribution of microtubules.

Maria S Tikhomirova, Avihay Kadosh, Aksel J Saukko-Paavola, Tom Shemesh, Robin W Klemm

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed, 1 pooled it
4.7field-weighted citation impact, top 4% 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

21 citing papers in PubMed, 1 synthesis or guideline pooled it, 44 citations in OpenAlex.

  1. Stay in touch with the endoplasmic reticulum.Science China. Life sciences · 2024
    Pooled it
  2. Article
  3. Review
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. The endoplasmic reticulum as an active liquid network.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Luminal transport through intact endoplasmic reticulum limits the magnitude of localized CaProceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  17. Article
  18. Article
  19. Article
  20. 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

5 authors at 3 institutions in 3 countries.

Maria S TikhomirovaDepartment of Molecular Life Sciences, University of Zurich, CH-8057 Zurich, Switzerland.
Avihay KadoshFaculty of Biology, Technion-Israel Institute of Technology, Haifa 32000, Israel.
Aksel J Saukko-PaavolaDepartment of Physiology Anatomy and Genetics, University of Oxford, Oxford OX1 3PT, United Kingdom.ORCID 0000-0001-9996-6611
Tom ShemeshFaculty of Biology, Technion-Israel Institute of Technology, Haifa 32000, Israel.
Robin W KlemmDepartment of Molecular Life Sciences, University of Zurich, CH-8057 Zurich, Switzerland.ORCID 0000-0003-2313-8240
Technion – Israel Institute of Technology · ILUniversity of Zurich · CHUniversity of Oxford · GB

Funding

Biotechnology and Biological Sciences Research Council BB/T008784/1
6 · The paper itself

Abstract

The dynamic distribution of the microtubule (MT) cytoskeleton is crucial for the shape, motility, and internal organization of eukaryotic cells. However, the basic principles that control the subcellular position of MTs in mammalian interphase cells remain largely unknown. Here we show by a combination of microscopy and computational modeling that the dynamics of the endoplasmic reticulum (ER) plays an important role in distributing MTs in the cell. Specifically, our physics-based model of the ER–MT system reveals that spatial inhomogeneity in the density of ER tubule junctions results in an overall contractile force that acts on MTs and influences their distribution. At steady state, cells rapidly compensate for local variability of ER junction density by dynamic formation, release, and movement of ER junctions across the ER. Perturbation of ER junction tethering and fusion by depleting the ER fusogens called atlastins disrupts the dynamics of junction equilibration, rendering the ER–MT system unstable and causing the formation of MT bundles. Our study points to a mechanical role of ER dynamics in cellular organization and suggests a mechanism by which cells might dynamically regulate MT distribution in, e.g., motile cells or in the formation and maintenance of neuronal axons.

Indexed as

Endoplasmic ReticulumMicrotubulesAxonsCytoskeletonNeuronscellular organizationendoplasmic reticulummicrotubule bundlesmicrotubules

Identifiers

PMID35377783
PMCPMC9169640
OpenAlexW4224023355

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.