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IL-4 expressing cells are recruited to nerve after injury and promote regeneration.
- Source :
-
Experimental neurology [Exp Neurol] 2022 Jan; Vol. 347, pp. 113909. Date of Electronic Publication: 2021 Oct 28. - Publication Year :
- 2022
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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.<br /> (Copyright © 2021 Elsevier Inc. All rights reserved.)
- Subjects :
- Animals
Cells, Cultured
Eosinophils drug effects
Eosinophils immunology
Eosinophils metabolism
Ganglia, Spinal immunology
Ganglia, Spinal metabolism
Gene Expression Regulation
Injections, Intraperitoneal
Interleukin-4 immunology
Macrophages drug effects
Macrophages immunology
Macrophages metabolism
Male
Mice
Mice, Inbred C57BL
Mice, Knockout
Nerve Crush trends
Nerve Regeneration drug effects
Rats
Rats, Sprague-Dawley
Receptors, Interleukin-4 biosynthesis
Receptors, Interleukin-4 immunology
Sciatic Neuropathy drug therapy
Sciatic Neuropathy immunology
Interleukin-4 administration & dosage
Interleukin-4 biosynthesis
Nerve Regeneration physiology
Sciatic Neuropathy metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1090-2430
- Volume :
- 347
- Database :
- MEDLINE
- Journal :
- Experimental neurology
- Publication Type :
- Academic Journal
- Accession number :
- 34717939
- Full Text :
- https://doi.org/10.1016/j.expneurol.2021.113909