Evidence map›Paper›PMID 24411232›Full record

ArticleBiophysical journal2014

Actomyosin pulls to advance the nucleus in a migrating tissue cell.

Jun Wu, Ian A Kent, Nandini Shekhar, T J Chancellor, Agnes Mendonca, Richard B Dickinson, Tanmay P Lele

Abstract read
In one paragraph

Article in Biophysical journal, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing 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

42 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Article
  5. The Nuclear Lamina.Cold Spring Harbor perspectives in biology · 2022
    Review
  6. Review
  7. Wound healing of the corneal epithelium: a review.Asian biomedicine : research, reviews and news · 2021
    Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Mechanical Regulation of Nuclear Translocation in Migratory Neurons.Frontiers in cell and developmental biology · 2020
    Review
  15. Article
  16. Cell migration through three-dimensional confining pores: speed accelerations by deformation and recoil of the nucleus.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2019
    Article
  17. Emerging regulators of vascular smooth muscle cell migration.Journal of muscle research and cell motility · 2019
    Review
  18. Article
  19. Review
  20. Nuclear positioning in migrating fibroblasts.Seminars in cell & developmental biology · 2018
    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.

Jun WuDepartment of Chemical Engineering, University of Florida, Gainesville, Florida.
Ian A KentDepartment of Chemical Engineering, University of Florida, Gainesville, Florida.
Nandini ShekharDepartment of Chemical Engineering, University of Florida, Gainesville, Florida.
T J ChancellorDepartment of Chemical Engineering, University of Florida, Gainesville, Florida.
Agnes MendoncaDepartment of Chemical Engineering, University of Florida, Gainesville, Florida.
Richard B DickinsonDepartment of Chemical Engineering, University of Florida, Gainesville, Florida.
Tanmay P LeleDepartment of Chemical Engineering, University of Florida, Gainesville, Florida. Electronic address: tlele@che.ufl.edu.

Funding

SUBSTRATE RIGIDITY AND GENE EXPRESSION: Role of Nuclear TensionR01EB014869 · NIBIB · UNIVERSITY OF FLORIDA · PI LELE, TANMAY P. · 2012 to 2019
$3.4M
Cytoskeletal force generation on the nucleusR01GM102486 · NIGMS · UNIVERSITY OF FLORIDA · PI LELE, TANMAY P. · 2012 to 2015
$1.2M
NIBIB NIH HHS 5R01EB014869-02NIBIB NIH HHS R01 EB014869NIGMS NIH HHS R01 GM102486NIGMS NIH HHS R01GM102486-01
6 · The paper itself

Abstract

The cytoskeletal forces involved in translocating the nucleus in a migrating tissue cell remain unresolved. Previous studies have variously implicated actomyosin-generated pushing or pulling forces on the nucleus, as well as pulling by nucleus-bound microtubule motors. We found that the nucleus in an isolated migrating cell can move forward without any trailing-edge detachment. When a new lamellipodium was triggered with photoactivation of Rac1, the nucleus moved toward the new lamellipodium. This forward motion required both nuclear-cytoskeletal linkages and myosin activity. Apical or basal actomyosin bundles were found not to translate with the nucleus. Although microtubules dampen fluctuations in nuclear position, they are not required for forward translocation of the nucleus during cell migration. Trailing-edge detachment and pulling with a microneedle produced motion and deformation of the nucleus suggestive of a mechanical coupling between the nucleus and the trailing edge. Significantly, decoupling the nucleus from the cytoskeleton with KASH overexpression greatly decreased the frequency of trailing-edge detachment. Collectively, these results explain how the nucleus is moved in a crawling fibroblast and raise the possibility that forces could be transmitted from the front to the back of the cell through the nucleus.

Indexed as

Cell MovementActomyosinAnimalsCell Cycle ProteinsCell NucleusMiceMicrotubulesMotionNIH 3T3 CellsPseudopodiarac1 GTP-Binding ProteinActomyosinCell Cycle Proteinsrac1 GTP-Binding Protein

Identifiers

PMID24411232
PMCPMC3907209

What OpenQuestion holds

Textmetadata
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.