Evidence map›Paper›PMID 25274820›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2014

FAK is required for Schwann cell spreading on immature basal lamina to coordinate the radial sorting of peripheral axons with myelination.

Matthew Grove, Peter J Brophy

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
1.7field-weighted citation impact, top 18% 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

34 citing papers in PubMed, 42 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Schwann Cell Development and Myelination.Cold Spring Harbor perspectives in biology · 2024
    Review
  7. Review
  8. Article
  9. Article
  10. Review
  11. Article
  12. Melatonin signalling in Schwann cells during neuroregeneration.Frontiers in cell and developmental biology · 2022
    Review
  13. Article
  14. Review
  15. Peripheral Nerve Development and the Pathogenesis of Peripheral Neuropathy: the Sorting Point.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2021
    Review
  16. Review
  17. Review
  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

2 authors at 1 institution in 1 country.

Matthew GroveCentre for Neuroregeneration, University of Edinburgh, Edinburgh EH16 4SB, United Kingdom.
Peter J BrophyCentre for Neuroregeneration, University of Edinburgh, Edinburgh EH16 4SB, United Kingdom Peter.Brophy@ed.ac.uk.
University of Edinburgh · GB

Funding

Wellcome Trust
6 · The paper itself

Abstract

Without Focal Adhesion Kinase (FAK), developing murine Schwann cells (SCs) proliferate poorly, sort axons inefficiently, and cannot myelinate peripheral nerves. Here we show that FAK is required for the development of SCs when their basal lamina (BL) is fragmentary, but not when it is mature in vivo. Mutant SCs fail to spread on fragmentary BL during development in vivo, and this is phenocopied by SCs lacking functional FAK on low laminin (LN) in vitro. Furthermore, SCs without functional FAK initiate differentiation prematurely, both in vivo and in vitro. In contrast to their behavior on high levels of LN, SCs lacking functional FAK grown on low LN display reduced spreading, proliferation, and indicators of contractility (i.e., stress fibers, arcs, and focal adhesions) and are primed to differentiate. Growth of SCs lacking functional FAK on increasing LN concentrations in vitro revealed that differentiation is not regulated by G1 arrest but rather by cell spreading and the level of contractile actomyosin. The importance of FAK as a critical regulator of the specific response of developing SCs to fragmentary BL was supported by the ability of adult FAK mutant SCs to remyelinate demyelinated adult nerves on mature BL in vivo. We conclude that FAK promotes the spreading and actomyosin contractility of immature SCs on fragmentary BL, thus maintaining their proliferation, and preventing differentiation until they reach high density, thereby promoting radial sorting. Hence, FAK has a critical role in the response of SCs to limiting BL by promoting proliferation and preventing premature SC differentiation.

Indexed as

2',3'-Cyclic Nucleotide 3'-PhosphodiesteraseAnimalsBasement MembraneCell DifferentiationCells, CulturedCyclin-Dependent Kinase Inhibitor p27Disease Models, AnimalEmbryo, MammalianFemaleFlow CytometryFocal Adhesion Kinase 1Green Fluorescent ProteinsMaleMiceMice, Inbred C57BLMyelin Proteolipid Protein2',3'-Cyclic Nucleotide 3'-PhosphodiesteraseCdkn1b protein, mouseCnp protein, mouseCyclin-Dependent Kinase Inhibitor p27enhanced green fluorescent proteinFocal Adhesion Kinase 1Green Fluorescent ProteinsMyelin Proteolipid ProteinPlp1 protein, mousePtk2 protein, mousebasal laminaFAKmyelinationSchwann cell

Identifiers

PMID25274820
PMCPMC4180476
OpenAlexW2145071956

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.