Evidence map›Paper›PMID 27667364›Full record

ArticleCell systems2016

Vimentin Intermediate Filaments Template Microtubule Networks to Enhance Persistence in Cell Polarity and Directed Migration.

Zhuo Gan, Liya Ding, Christoph J Burckhardt, Jason Lowery, Assaf Zaritsky, Karlyndsay Sitterley, Andressa Mota, Nancy Costigliola, Colby G Starker, Daniel F Voytas and 3 more

Erratum issuedOpen access · bronzeAbstract read
In one paragraph

Article in Cell systems, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 125 papers.

0numbers the graph read from it
0cells of the map it votes in
125citing papers in PubMed
11.6field-weighted citation impact, top 1% 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

125 citing papers in PubMed, 242 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Vimentin Intermediate Filaments: A Paradigm Shift From Static Structure to Dynamic Cytoplasmic Network.BioEssays : news and reviews in molecular, cellular and developmental biology · 2026
    Review
  11. Article
  12. Article
  13. A neuron-astrocyte signaling axis in the ACC sustains diabetic neuropathic pain.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  14. Article
  15. Regulatory T cells attenuate astrogliosis via IL-10/STAT3/PKC/vimentin signaling and promote neurological recovery after spinal cord injury.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2026
    Article
  16. Article
  17. Galectin-related protein, a key contributor, drives diabetes-associated neuropathic pain.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  18. Article
  19. Article
  20. Review

65 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors at 4 institutions in 1 country.

Zhuo GanDepartment of Cell Biology, University of Texas Southwestern Medical Center at Dallas, Dallas, TX 75235, USA.
Liya DingDepartment of Cell Biology, University of Texas Southwestern Medical Center at Dallas, Dallas, TX 75235, USA; Department of Cell Biology, Harvard Medical School, Boston, MA 02115, USA.
Christoph J BurckhardtDepartment of Cell Biology, University of Texas Southwestern Medical Center at Dallas, Dallas, TX 75235, USA; Department of Cell Biology, Harvard Medical School, Boston, MA 02115, USA.
Jason LoweryDepartment of Cell and Molecular Biology, Feinberg School of Medicine, Northwestern University, Evanston, IL 60208, USA.
Assaf ZaritskyDepartment of Cell Biology, University of Texas Southwestern Medical Center at Dallas, Dallas, TX 75235, USA.
Karlyndsay SitterleyDepartment of Cell Biology, Harvard Medical School, Boston, MA 02115, USA.
Andressa MotaDepartment of Cell Biology, Harvard Medical School, Boston, MA 02115, USA.
Nancy CostigliolaDepartment of Cell Biology, Harvard Medical School, Boston, MA 02115, USA.
Colby G StarkerDepartment of Genetics, Cell Biology & Development and Center for Genome Engineering, University of Minnesota, Minneapolis, MN 55455, USA.
Daniel F VoytasDepartment of Genetics, Cell Biology & Development and Center for Genome Engineering, University of Minnesota, Minneapolis, MN 55455, USA.
Jessica TytellDepartment of Cell Biology, Harvard Medical School, Boston, MA 02115, USA.
Robert D GoldmanDepartment of Cell and Molecular Biology, Feinberg School of Medicine, Northwestern University, Evanston, IL 60208, USA.
Gaudenz DanuserDepartment of Cell Biology, University of Texas Southwestern Medical Center at Dallas, Dallas, TX 75235, USA; Department of Cell Biology, Harvard Medical School, Boston, MA 02115, USA. Electronic address: gaudenz.danuser@utsouthwestern.edu.
Harvard University · USNorthwestern University · USThe University of Texas Southwestern Medical Center · USUniversity of Minnesota · US

Funding

UT Southwestern Medical Center Simmons Comprehensive Cancer CenterP30CA142543 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI Sandi Leigh Pruitt · 2010 to 2026
$53.7M
Structural basis of the specific protein-protein interactions underlying IF assemP01GM096971 · NIGMS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI GOLDMAN, ROBERT D · 2011 to 2021
$16.8M
NCI NIH HHS P30 CA142543NIGMS NIH HHS P01 GM096971
6 · The paper itself

Abstract

Increased expression of vimentin intermediate filaments (VIFs) enhances directed cell migration, but the mechanism behind VIFs' effect on motility is not understood. VIFs interact with microtubules, whose organization contributes to polarity maintenance in migrating cells. Here, we characterize the dynamic coordination of VIF and microtubule networks in wounded monolayers of retinal pigment epithelial cells. By genome editing, we fluorescently labeled endogenous vimentin and α-tubulin, and we developed computational image analysis to delineate architecture and interactions of the two networks. Our results show that VIFs assemble an ultrastructural copy of the previously polarized microtubule network. Because the VIF network is long-lived compared to the microtubule network, VIFs template future microtubule growth along previous microtubule tracks, thus providing a feedback mechanism that maintains cell polarity. VIF knockdown prevents cells from polarizing and migrating properly during wound healing. We suggest that VIFs' templating function establishes a memory in microtubule organization that enhances persistence in cell polarization in general and migration in particular.

Indexed as

MicrotubulesCell MovementCell PolarityCells, CulturedCytoskeletonIntermediate FilamentsMicrotubule-Associated ProteinsTubulinVimentinMicrotubule-Associated ProteinsTubulinVimentin

Identifiers

PMID27667364
PMCPMC5055390
OpenAlexW2517856915

What OpenQuestion holds

Textmetadata
LicenceTDM
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.