Evidence map›Paper›PMID 36355066›Full record

ArticleDevelopment (Cambridge, England)2022

Discoidin domain receptor regulates ensheathment, survival and caliber of peripheral axons.

Megan M Corty, Alexandria L Hulegaard, Jo Q Hill, Amy E Sheehan, Sue A Aicher, Marc R Freeman

Open access · hybridAbstract read
In one paragraph

Article in Development (Cambridge, England), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

11 citing papers in PubMed, 19 citations in OpenAlex.

  1. TheeLife · 2026
    Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Glia as Functional Barriers and Signaling Intermediaries.Cold Spring Harbor perspectives in biology · 2024
    Review
  7. Review
  8. Drosophila glia take shape to sculpt the nervous system.Current opinion in neurobiology · 2023
    Review
  9. Article
  10. A nerve-wracking buzz: lessons fromFrontiers in aging neuroscience · 2023
    Review
  11. 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

6 authors at 1 institution in 1 country.

Megan M CortyVollum Institute, Oregon Health & Science University, Portland, OR 97239, USA.ORCID 0000-0002-5463-6739
Alexandria L HulegaardVollum Institute, Oregon Health & Science University, Portland, OR 97239, USA.ORCID 0000-0002-3886-3341
Jo Q HillDepartment of Chemical Physiology & Biochemistry, Oregon Health & Science University, Portland, OR 97239, USA.ORCID 0000-0002-7094-2031
Amy E SheehanVollum Institute, Oregon Health & Science University, Portland, OR 97239, USA.
Sue A AicherDepartment of Chemical Physiology & Biochemistry, Oregon Health & Science University, Portland, OR 97239, USA.ORCID 0000-0001-5310-4055
Marc R FreemanVollum Institute, Oregon Health & Science University, Portland, OR 97239, USA.ORCID 0000-0003-3481-3715
Oregon Health & Science University · US

Funding

Ultrastructure and Single Particle Microscopy CoreP30NS061800 · NINDS · OREGON HEALTH & SCIENCE UNIVERSITY · PI AICHER, SUE A · 2009 to 2020
$6.6M
Molecular Mechanisms of Axon DegenerationR01NS059991 · NINDS · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI FREEMAN, MARC R · 2008 to 2023
$5.4M
How do non-myelinating glia ensheath axons?R01NS112215 · NINDS · OREGON HEALTH & SCIENCE UNIVERSITY · PI FREEMAN, MARC R · 2019 to 2023
$1.7M
Howard Hughes Medical InstituteNINDS NIH HHS P30 NS061800NINDS NIH HHS R01 NS059991NINDS NIH HHS R01 NS112215
6 · The paper itself

Abstract

Most invertebrate axons and small-caliber axons in mammalian peripheral nerves are unmyelinated but still ensheathed by glia. Here, we use Drosophila wrapping glia to study the development and function of non-myelinating axon ensheathment, which is poorly understood. Selective ablation of these glia from peripheral nerves severely impaired larval locomotor behavior. In an in vivo RNA interference screen to identify glial genes required for axon ensheathment, we identified the conserved receptor tyrosine kinase Discoidin domain receptor (Ddr). In larval peripheral nerves, loss of Ddr resulted in severely reduced ensheathment of axons and reduced axon caliber, and we found a strong dominant genetic interaction between Ddr and the type XV/XVIII collagen Multiplexin (Mp), suggesting that Ddr functions as a collagen receptor to drive axon wrapping. In adult nerves, loss of Ddr decreased long-term survival of sensory neurons and significantly reduced axon caliber without overtly affecting ensheathment. Our data establish essential roles for non-myelinating glia in nerve development, maintenance and function, and identify Ddr as a key regulator of axon-glia interactions during ensheathment and establishment of axon caliber.

Indexed as

AxonsDrosophila ProteinsAnimalsDiscoidin Domain ReceptorsDrosophilaMammalsNeurogliaPeripheral NervesDiscoidin Domain ReceptorsDrosophila ProteinsAxon ensheathmentDrosophilaMultiplexinRemak Schwann cellWrapping glia

Identifiers

PMID36355066
PMCPMC10112903
OpenAlexW4308682326

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.