Evidence map›Paper›PMID 28468979›Full record

ArticleMolecular biology of the cell2017

Increased lateral microtubule contact at the cell cortex is sufficient to drive mammalian spindle elongation.

Joshua Guild, Miriam B Ginzberg, Christina L Hueschen, Timothy J Mitchison, Sophie Dumont

Abstract read
In one paragraph

Article in Molecular biology of the cell, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
–field-weighted citation impact
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

26 citing papers in PubMed.

  1. Article
  2. Cell confinement initiates a delayed but heritable loss of chromosomes.bioRxiv : the preprint server for biology · 2026
    Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Mechanisms underlying spindle assembly and robustness.Nature reviews. Molecular cell biology · 2023
    Review
  10. Article
  11. Article
  12. Coupling of microtubule bundles isolates them from local disruptions to set the structural stability of the anaphase spindle.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  13. Article
  14. Article
  15. Anaphase B: Long-standing models meet new concepts.Seminars in cell & developmental biology · 2021
    Review
  16. Chemical tools for dissecting cell division.Nature chemical biology · 2021
    Review
  17. Cellular Pushing Forces during Mitosis Drive Mitotic Elongation in Collagen Gels.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2021
    Article
  18. Article
  19. Article
  20. Article
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.

Joshua GuildDepartment of Cell and Tissue Biology, University of California, San Francisco, San Francisco, CA 94131.
Miriam B GinzbergDepartment of Systems Biology, Harvard Medical School, Boston, MA 02115.
Christina L HueschenDepartment of Cell and Tissue Biology, University of California, San Francisco, San Francisco, CA 94131.
Timothy J MitchisonDepartment of Systems Biology, Harvard Medical School, Boston, MA 02115.
Sophie DumontDepartment of Cell and Tissue Biology, University of California, San Francisco, San Francisco, CA 94131 sophie.dumont@ucsf.edu.

Funding

MICROTUBULE DYNAMICS AND MITOTIC MECHANISMR01GM039565 · NIGMS · UNIVERSITY OF CALIFORNIA SAN FRANCISCO · PI MITCHISON, TIMOTHY J · 1988 to 2018
$6.2M
Rewiring cellular architecture to probe mechanical signal processing at kinetochoresDP2GM119177 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI DUMONT, SOPHIE · 2015 to 2015
$2.4M
Molecular Basis and Role of Indirect Chromosome Segregation in Hyperploid Cancer CellsF31CA200277 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI HUESCHEN, CHRISTINA LYNN · 2015 to 2017
$106k
NCI NIH HHS F31 CA200277NIGMS NIH HHS DP2 GM119177NIGMS NIH HHS R01 GM039565
6 · The paper itself

Abstract

The spindle is a dynamic structure that changes its architecture and size in response to biochemical and physical cues. For example, a simple physical change, cell confinement, can trigger centrosome separation and increase spindle steady-state length at metaphase. How this occurs is not understood, and is the question we pose here. We find that metaphase and anaphase spindles elongate at the same rate when confined, suggesting that similar elongation forces can be generated independent of biochemical and spindle structural differences. Furthermore, this elongation does not require bipolar spindle architecture or dynamic microtubules. Rather, confinement increases numbers of astral microtubules laterally contacting the cortex, shifting contact geometry from "end-on" to "side-on." Astral microtubules engage cortically anchored motors along their length, as demonstrated by outward sliding and buckling after ablation-mediated release from the centrosome. We show that dynein is required for confinement-induced spindle elongation, and both chemical and physical centrosome removal demonstrate that astral microtubules are required for such spindle elongation and its maintenance. Together the data suggest that promoting lateral cortex-microtubule contacts increases dynein-mediated force generation and is sufficient to drive spindle elongation. More broadly, changes in microtubule-to-cortex contact geometry could offer a mechanism for translating changes in cell shape into dramatic intracellular remodeling.

Indexed as

AnaphaseAnimalsCaenorhabditis elegansCell Culture TechniquesCell CycleCell ShapeCentrosomeDyneinsKinesinsMammalsMetaphaseMicrotubule-Associated ProteinsMicrotubulesSpindle ApparatusDyneinsKinesinsMicrotubule-Associated Proteins

Identifiers

PMID28468979
PMCPMC5541847

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.