Evidence map›Paper›PMID 37590333›Full record

ArticlePLoS biology2023

Target-selective vertebrate motor axon regeneration depends on interaction with glial cells at a peripheral nerve plexus.

Lauren J Walker, Camilo Guevara, Koichi Kawakami, Michael Granato

Open access · goldAbstract read
In one paragraph

Article in PLoS biology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.4field-weighted citation impact, top 41% 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

3 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors at 2 institutions in 2 countries.

Lauren J WalkerDepartment of Cell and Developmental Biology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, United States of America.ORCID 0000-0003-3844-4275
Camilo GuevaraDepartment of Cell and Developmental Biology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, United States of America.
Koichi KawakamiLaboratory of Molecular and Developmental Biology, National Institute of Genetics, and Department of Genetics, The Graduate University for Advanced Studies (SOKENDAI), Mishima, Shizuoka, Japan.
Michael GranatoDepartment of Cell and Developmental Biology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, United States of America.ORCID 0000-0003-3878-9468
University of Pennsylvania · USNational Institute of Genetics · JP

Funding

Genetic analysis of axonal regenerationR01EY024861 · NEI · UNIVERSITY OF PENNSYLVANIA · PI GRANATO, MICHAEL · 2014 to 2023
$4.1M
Molecular genetic mechanisms of spontaneous spinal cord regenerationR01NS097914 · NINDS · UNIVERSITY OF PENNSYLVANIA · PI Michael Granato · 2017 to 2026
$3.3M
Molecular and Cellular Mechanisms of Target-Selective Axon Regeneration Through a PlexusK01NS119496 · NINDS · UNIVERSITY OF PENNSYLVANIA · PI WALKER, LAUREN J · 2021 to 2023
$365k
NEI NIH HHS R01 EY024861NINDS NIH HHS K01 NS119496NINDS NIH HHS R01 NS097914
6 · The paper itself

Abstract

A critical step for functional recovery from peripheral nerve injury is for regenerating axons to connect with their pre-injury targets. Reestablishing pre-injury target specificity is particularly challenging for limb-innervating axons as they encounter a plexus, a network where peripheral nerves converge, axons from different nerves intermingle, and then re-sort into target-specific bundles. Here, we examine this process at a plexus located at the base of the zebrafish pectoral fin, equivalent to tetrapod forelimbs. Using live cell imaging and sparse axon labeling, we find that regenerating motor axons from 3 nerves coalesce into the plexus. There, they intermingle and sort into distinct branches, and then navigate to their original muscle domains with high fidelity that restores functionality. We demonstrate that this regeneration process includes selective retraction of mistargeted axons, suggesting active correction mechanisms. Moreover, we find that Schwann cells are enriched and associate with axons at the plexus, and that Schwann cell ablation during regeneration causes profound axonal mistargeting. Our data provide the first real-time account of regenerating vertebrate motor axons navigating a nerve plexus and reveal a previously unappreciated role for Schwann cells to promote axon sorting at a plexus during regeneration.

Indexed as

AxonsZebrafishAnimalsNerve RegenerationNeurogliaPeripheral Nerves

Identifiers

PMID37590333
PMCPMC10464982
OpenAlexW4385932271

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.