Evidence map›Paper›PMID 34717939›Full record

ArticleExperimental neurology2022

IL-4 expressing cells are recruited to nerve after injury and promote regeneration.

Deng Pan, Lauren Schellhardt, Jesús A Acevedo-Cintron, Daniel Hunter, Alison K Snyder-Warwick, Susan E Mackinnon, Matthew D Wood

Open access · greenAbstract read
In one paragraph

Article in Experimental neurology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
3.3field-weighted citation impact, top 7% 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

24 citing papers in PubMed, 41 citations in OpenAlex.

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  12. Generation and repair of thymic epithelial cells.The Journal of experimental medicine · 2024
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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

7 authors at 1 institution in 1 country.

Deng PanDivision of Plastic and Reconstructive Surgery, Department of Surgery, Washington University School of Medicine, St. Louis, MO 63110, USA.
Lauren SchellhardtDivision of Plastic and Reconstructive Surgery, Department of Surgery, Washington University School of Medicine, St. Louis, MO 63110, USA.
Jesús A Acevedo-CintronDivision of Plastic and Reconstructive Surgery, Department of Surgery, Washington University School of Medicine, St. Louis, MO 63110, USA.
Daniel HunterDivision of Plastic and Reconstructive Surgery, Department of Surgery, Washington University School of Medicine, St. Louis, MO 63110, USA.
Alison K Snyder-WarwickDivision of Plastic and Reconstructive Surgery, Department of Surgery, Washington University School of Medicine, St. Louis, MO 63110, USA.
Susan E MackinnonDivision of Plastic and Reconstructive Surgery, Department of Surgery, Washington University School of Medicine, St. Louis, MO 63110, USA.
Matthew D WoodDivision of Plastic and Reconstructive Surgery, Department of Surgery, Washington University School of Medicine, St. Louis, MO 63110, USA. Electronic address: woodmd@wustl.edu.
Washington University in St. Louis · US

Funding

THE ROLE OF SCHWANN CELL SENESCENCE IN PERIPHERAL NERVE REGENERATIONR01NS086773 · NINDS · WASHINGTON UNIVERSITY · PI MACKINNON, SUSAN E · 2015 to 2019
$2.1M
T cell roles in regeneration across nerve graft alternativesR01NS115960 · NINDS · WASHINGTON UNIVERSITY · PI WOOD, MATTHEW D. · 2020 to 2024
$1.8M
Investigation of Terminal Schwann Cell Function in Homeostasis and InjuryK08NS096232 · NINDS · WASHINGTON UNIVERSITY · PI SNYDER-WARWICK, ALISON K · 2017 to 2020
$717k
NINDS NIH HHS K08 NS096232NINDS NIH HHS R01 NS086773NINDS NIH HHS R01 NS115960
6 · The paper itself

Abstract

Interleukin-4 (IL-4) has garnered interest as a cytokine that mediates regeneration across multiple tissues including peripheral nerve. Within nerve, we previously showed endogenous IL-4 was critical to regeneration across nerve gaps. Here, we determined a generalizable role of IL-4 in nerve injury and regeneration. In wild-type (WT) mice receiving a sciatic nerve crush, IL-4 expressing cells preferentially accumulated within the injured nerve compared to affected sites proximal, such as dorsal root ganglia (DRGs), or distal muscle. Immunohistochemistry and flow cytometry confirmed that eosinophils (CD45+, CD11b+, CD64-, Siglec-F+) were sources of IL-4 expression. Examination of targets for IL-4 within nerve revealed macrophages, as well as subsets of neurons expressed IL-4R, while Schwann cells expressed limited IL-4R. Dorsal root ganglia cultures were exposed to IL-4 and demonstrated an increased proportion of neurons that extended axons compared to cultures without IL-4 (control), as well as longer myelinated axons compared to cultures without IL-4. The role of endogenous IL-4 during nerve injury and regeneration in vivo was assessed following a sciatic nerve crush using IL-4 knockout (KO) mice. Loss of IL-4 affected macrophage accumulation within injured nerve compared to WT mice, as well as shifted macrophage phenotype towards a CD206- phenotype with altered gene expression. Furthermore, this loss of IL-4 delayed initial axon regeneration from the injury crush site and subsequently delayed functional recovery and re-innervation of neuromuscular junctions compared to wild-type mice. Given the role of endogenous IL-4 in nerve regeneration, exogenous IL-4 was administered daily to WT mice following a nerve crush to examine regeneration. Daily IL-4 administration increased early axonal extension and CD206+ macrophage accumulation but did not alter functional recovery compared to untreated mice. Our data demonstrate IL-4 promotes nerve regeneration and recovery after injury.

Indexed as

AnimalsCells, CulturedEosinophilsGanglia, SpinalGene Expression RegulationInjections, IntraperitonealInterleukin-4MacrophagesMaleMiceMice, Inbred C57BLMice, KnockoutNerve CrushNerve RegenerationRatsRats, Sprague-DawleyInterleukin-4Receptors, Interleukin-4Functional recoveryIL-4InterleukinMacrophageNerve crushNerve regenerationPeripheral nerve

Identifiers

PMID34717939
PMCPMC8887027
OpenAlexW3209095201

What OpenQuestion holds

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LicenceTDM
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.