Evidence map›Paper›PMID 25995380›Full record

ArticleMolecular biology of the cell2015

An ELMO2-RhoG-ILK network modulates microtubule dynamics.

Bradley C Jackson, Iordanka A Ivanova, Lina Dagnino

Open access · greenAbstract read
In one paragraph

Article in Molecular biology of the cell, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.7field-weighted citation impact, top 17% 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, 28 citations in OpenAlex.

  1. Targeting of ELMO2 by thebioRxiv : the preprint server for biology · 2026
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  14. RhoG-ELMO1-RAC1 is involved in phagocytosis suppressed by mono-butyl phthalate in TM4 cells.Environmental science and pollution research international · 2018
    Article
  15. Article
  16. A reporter mouse model forBiology open · 2017
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  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

3 authors at 1 institution in 1 country.

Bradley C JacksonDepartment of Physiology and Pharmacology, Children's Health Research Institute, and Lawson Health Research Institute, University of Western Ontario, London, ON N6A 5C1, Canada.
Iordanka A IvanovaDepartment of Physiology and Pharmacology, Children's Health Research Institute, and Lawson Health Research Institute, University of Western Ontario, London, ON N6A 5C1, Canada.
Lina DagninoDepartment of Physiology and Pharmacology, Children's Health Research Institute, and Lawson Health Research Institute, University of Western Ontario, London, ON N6A 5C1, Canada ldagnino@uwo.ca.
Western University · CA

Funding

Canadian Institutes of Health Research
6 · The paper itself

Abstract

ELMO2 belongs to a family of scaffold proteins involved in phagocytosis and cell motility. ELMO2 can simultaneously bind integrin-linked kinase (ILK) and RhoG, forming tripartite ERI complexes. These complexes are involved in promoting β1 integrin-dependent directional migration in undifferentiated epidermal keratinocytes. ELMO2 and ILK have also separately been implicated in microtubule regulation at integrin-containing focal adhesions. During differentiation, epidermal keratinocytes cease to express integrins, but ERI complexes persist. Here we show an integrin-independent role of ERI complexes in modulation of microtubule dynamics in differentiated keratinocytes. Depletion of ERI complexes by inactivating the Ilk gene in these cells reduces microtubule growth and increases the frequency of catastrophe. Reciprocally, exogenous expression of ELMO2 or RhoG stabilizes microtubules, but only if ILK is also present. Mechanistically, activation of Rac1 downstream from ERI complexes mediates their effects on microtubule stability. In this pathway, Rac1 serves as a hub to modulate microtubule dynamics through two different routes: 1) phosphorylation and inactivation of the microtubule-destabilizing protein stathmin and 2) phosphorylation and inactivation of GSK-3β, which leads to the activation of CRMP2, promoting microtubule growth. At the cellular level, the absence of ERI species impairs Ca(2+)-mediated formation of adherens junctions, critical to maintaining mechanical integrity in the epidermis. Our findings support a key role for ERI species in integrin-independent stabilization of the microtubule network in differentiated keratinocytes.

Indexed as

Signal TransductionAdaptor Proteins, Signal TransducingAdherens JunctionsAnimalsCytoskeletal ProteinsGlycogen Synthase Kinase 3Glycogen Synthase Kinase 3 betaGTP PhosphohydrolasesIntercellular Signaling Peptides and ProteinsKeratinocytesMiceMice, Mutant StrainsMicrotubulesNerve Tissue ProteinsNeuropeptidesProtein Serine-Threonine KinasesAdaptor Proteins, Signal Transducingcollapsin response mediator protein-2Cytoskeletal ProteinsElmo2 protein, mouseGlycogen Synthase Kinase 3Glycogen Synthase Kinase 3 betaGsk3b protein, mouseGTP PhosphohydrolasesIntercellular Signaling Peptides and ProteinsNerve Tissue ProteinsNeuropeptidesProtein Serine-Threonine Kinasesrac1 GTP-Binding ProteinRac1 protein, mouseRhog protein, mouserho GTP-Binding ProteinsScaffold Protein ILKStathmin

Identifiers

PMID25995380
PMCPMC4501367
OpenAlexW2155547024

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.