Evidence map›Paper›PMID 31278268›Full record

ArticleNature communications2019

Myelinating Schwann cells ensheath multiple axons in the absence of E3 ligase component Fbxw7.

Breanne L Harty, Fernanda Coelho, Sarah E Pease-Raissi, Amit Mogha, Sarah D Ackerman, Amy L Herbert, Robert W Gereau, Judith P Golden, David A Lyons, Jonah R Chan and 1 more

Abstract read
In one paragraph

Article in Nature communications, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing 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

30 citing papers in PubMed.

  1. Article
  2. Review
  3. Glia of the heart's nervous system.Nature reviews. Neuroscience · 2025
    Review
  4. Article
  5. Article
  6. Gut microbiota regulates optic nerve fiber myelination.Frontiers in cell and developmental biology · 2025
    Article
  7. Review
  8. Targeting the Hippo pathway in Schwann cells ameliorates peripheral nerve degeneration via a polypharmacological mechanism.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2024
    Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Melatonin signalling in Schwann cells during neuroregeneration.Frontiers in cell and developmental biology · 2022
    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

11 authors.

Breanne L HartyThaden School, 410 SE Staggerwing Lane, Bentonville, AR, 72712, USA.
Fernanda CoelhoVollum Institute, Oregon Health & Science University, 3181 SW Sam Jackson Park Rd., Portland, OR, 97239, USA.ORCID http://orcid.org/0000-0003-1310-002X
Sarah E Pease-RaissiDepartment of Neurology, Weill Institute for Neuroscience, University of California San Francisco, 675 Nelson Rising Lane, San Francisco, CA, 94158, USA.
Amit MoghaVollum Institute, Oregon Health & Science University, 3181 SW Sam Jackson Park Rd., Portland, OR, 97239, USA.
Sarah D AckermanDepartment of Developmental Biology, Washington University School of Medicine, 660S. Euclid Ave., St. Louis, MO, 63110, USA.
Amy L HerbertDepartment of Developmental Biology, Washington University School of Medicine, 660S. Euclid Ave., St. Louis, MO, 63110, USA.
Robert W GereauDepartment of Anesthesiology, Washington University Pain Center, 660S. Euclid Ave., St. Louis, MO, 63110, USA.ORCID http://orcid.org/0000-0002-5428-4251
Judith P GoldenDepartment of Anesthesiology, Washington University Pain Center, 660S. Euclid Ave., St. Louis, MO, 63110, USA.
David A LyonsCentre for Brain Discovery Sciences, MS Society Centre for Translational Research, Euan MacDonald Centre for Motor Neurone Disease Research, University of Edinburgh, 49 Little France Crescent, Edinburgh, EH16 4SB, UK.ORCID http://orcid.org/0000-0003-1166-4454
Jonah R ChanDepartment of Neurology, Weill Institute for Neuroscience, University of California San Francisco, 675 Nelson Rising Lane, San Francisco, CA, 94158, USA.ORCID http://orcid.org/0000-0002-2176-1242
Kelly R MonkDepartment of Developmental Biology, Washington University School of Medicine, 660S. Euclid Ave., St. Louis, MO, 63110, USA. monk@ohsu.edu.

Funding

MECHANISMS OF PERIPHERAL MGLUR MODULATION OF NOCICEPTIONR01NS042595 · NINDS · WASHINGTON UNIVERSITY · PI GEREAU, ROBERT W · 2002 to 2017
$5.2M
THE ESTABLISHMENT OF SCHWANN CELL POLARITY AND THE INITIATION OF MYELINATIONR01NS062796 · NINDS · UNIVERSITY OF SOUTHERN CALIFORNIA · PI CHAN, JONAH R · 2008 to 2018
$3.4M
Chemical and genetic screens for modulators of nervous system development and myelinationR01HD080601 · NICHD · WASHINGTON UNIVERSITY · PI MONK, KELLY R · 2014 to 2018
$1.6M
Myo-inositol regulation of myelination in development and hypoxic newborn brain injuryF32HD098829 · NICHD · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI RAISSI, SARAH E · 2019 to 2022
$245k
Gpr56 is a regulator of glial cell development and myelinationF31NS087801 · NINDS · WASHINGTON UNIVERSITY · PI ACKERMAN, SARAH D · 2014 to 2016
$68k
Control of myelinating glial cell development by actr10F31NS096814 · NINDS · WASHINGTON UNIVERSITY · PI HERBERT, AMY · 2016 to 2017
$61k
MOLECULAR CONTROL OF MYELINATING GLIAL CELL DEVELOPMENT BY FBXW7F31NS094004 · NINDS · WASHINGTON UNIVERSITY · PI HARTY, BREANNE LEIGH · 2015 to 2016
$52k
NICHD NIH HHS F32 HD098829NICHD NIH HHS R01 HD080601NINDS NIH HHS F31 NS087801NINDS NIH HHS F31 NS094004NINDS NIH HHS F31 NS096814NINDS NIH HHS R01 NS042595NINDS NIH HHS R01 NS062796U.S. Department of Health & Human Services | NIH | National Institute of Neurological Disorders and Stroke (NINDS) R01NS062796Wellcome Trust 102836/Z/13/Z
6 · The paper itself

Abstract

In the central nervous system (CNS), oligodendrocytes myelinate multiple axons; in the peripheral nervous system (PNS), Schwann cells (SCs) myelinate a single axon. Why are the myelinating potentials of these glia so fundamentally different? Here, we find that loss of Fbxw7, an E3 ubiquitin ligase component, enhances the myelinating potential of SCs. Fbxw7 mutant SCs make thicker myelin sheaths and sometimes appear to myelinate multiple axons in a fashion reminiscent of oligodendrocytes. Several Fbxw7 mutant phenotypes are due to dysregulation of mTOR; however, the remarkable ability of mutant SCs to ensheathe multiple axons is independent of mTOR signaling. This indicates distinct roles for Fbxw7 in SC biology including modes of axon interactions previously thought to fundamentally distinguish myelinating SCs from oligodendrocytes. Our data reveal unexpected plasticity in the myelinating potential of SCs, which may have important implications for our understanding of both PNS and CNS myelination and myelin repair.

Indexed as

AnimalsAxonsF-Box-WD Repeat-Containing Protein 7MiceMice, Inbred C57BLMice, KnockoutMicroscopy, Electron, TransmissionModels, AnimalMyelin SheathSciatic NerveF-Box-WD Repeat-Containing Protein 7Fbxw7 protein, mouse

Identifiers

PMID31278268
PMCPMC6611888

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.