Schwann Cell Role in Selectivity of Nerve Regeneration

Peripheral nerve injuries result in the loss of the motor, sensory and autonomic functions of the denervated segments of the body. Neurons can regenerate after peripheral axotomy, but inaccuracy in reinnervation causes a permanent loss of function that impairs complete recovery. Thus, understanding...

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Main Authors: Sara Bolívar, Xavier Navarro, Esther Udina
Format: Article
Language:English
Published: MDPI AG 2020-09-01
Series:Cells
Subjects:
Online Access:https://www.mdpi.com/2073-4409/9/9/2131
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author Sara Bolívar
Xavier Navarro
Esther Udina
author_facet Sara Bolívar
Xavier Navarro
Esther Udina
author_sort Sara Bolívar
collection DOAJ
description Peripheral nerve injuries result in the loss of the motor, sensory and autonomic functions of the denervated segments of the body. Neurons can regenerate after peripheral axotomy, but inaccuracy in reinnervation causes a permanent loss of function that impairs complete recovery. Thus, understanding how regenerating axons respond to their environment and direct their growth is essential to improve the functional outcome of patients with nerve lesions. Schwann cells (SCs) play a crucial role in the regeneration process, but little is known about their contribution to specific reinnervation. Here, we review the mechanisms by which SCs can differentially influence the regeneration of motor and sensory axons. Mature SCs express modality-specific phenotypes that have been associated with the promotion of selective regeneration. These include molecular markers, such as L2/HNK-1 carbohydrate, which is differentially expressed in motor and sensory SCs, or the neurotrophic profile after denervation, which differs remarkably between SC modalities. Other important factors include several molecules implicated in axon-SC interaction. This cell–cell communication through adhesion (e.g., polysialic acid) and inhibitory molecules (e.g., MAG) contributes to guiding growing axons to their targets. As many of these factors can be modulated, further research will allow the design of new strategies to improve functional recovery after peripheral nerve injuries.
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spelling doaj.art-8fb2b6d4eb2b427aa1cf6a2e63f0431d2023-11-20T14:24:06ZengMDPI AGCells2073-44092020-09-0199213110.3390/cells9092131Schwann Cell Role in Selectivity of Nerve RegenerationSara Bolívar0Xavier Navarro1Esther Udina2Institute of Neurosciences, Department Cell Biology, Physiology and Immunology, Universitat Autònoma de Barcelona, and Centro de Investigación Biomédica en Red sobre Enfermedades Neurodegenerativas (CIBERNED), 08193 Bellaterra, SpainInstitute of Neurosciences, Department Cell Biology, Physiology and Immunology, Universitat Autònoma de Barcelona, and Centro de Investigación Biomédica en Red sobre Enfermedades Neurodegenerativas (CIBERNED), 08193 Bellaterra, SpainInstitute of Neurosciences, Department Cell Biology, Physiology and Immunology, Universitat Autònoma de Barcelona, and Centro de Investigación Biomédica en Red sobre Enfermedades Neurodegenerativas (CIBERNED), 08193 Bellaterra, SpainPeripheral nerve injuries result in the loss of the motor, sensory and autonomic functions of the denervated segments of the body. Neurons can regenerate after peripheral axotomy, but inaccuracy in reinnervation causes a permanent loss of function that impairs complete recovery. Thus, understanding how regenerating axons respond to their environment and direct their growth is essential to improve the functional outcome of patients with nerve lesions. Schwann cells (SCs) play a crucial role in the regeneration process, but little is known about their contribution to specific reinnervation. Here, we review the mechanisms by which SCs can differentially influence the regeneration of motor and sensory axons. Mature SCs express modality-specific phenotypes that have been associated with the promotion of selective regeneration. These include molecular markers, such as L2/HNK-1 carbohydrate, which is differentially expressed in motor and sensory SCs, or the neurotrophic profile after denervation, which differs remarkably between SC modalities. Other important factors include several molecules implicated in axon-SC interaction. This cell–cell communication through adhesion (e.g., polysialic acid) and inhibitory molecules (e.g., MAG) contributes to guiding growing axons to their targets. As many of these factors can be modulated, further research will allow the design of new strategies to improve functional recovery after peripheral nerve injuries.https://www.mdpi.com/2073-4409/9/9/2131axonSchwann cellregenerationaxon-glia interactionsperipheral nerve injuryreinnervation accuracy
spellingShingle Sara Bolívar
Xavier Navarro
Esther Udina
Schwann Cell Role in Selectivity of Nerve Regeneration
Cells
axon
Schwann cell
regeneration
axon-glia interactions
peripheral nerve injury
reinnervation accuracy
title Schwann Cell Role in Selectivity of Nerve Regeneration
title_full Schwann Cell Role in Selectivity of Nerve Regeneration
title_fullStr Schwann Cell Role in Selectivity of Nerve Regeneration
title_full_unstemmed Schwann Cell Role in Selectivity of Nerve Regeneration
title_short Schwann Cell Role in Selectivity of Nerve Regeneration
title_sort schwann cell role in selectivity of nerve regeneration
topic axon
Schwann cell
regeneration
axon-glia interactions
peripheral nerve injury
reinnervation accuracy
url https://www.mdpi.com/2073-4409/9/9/2131
work_keys_str_mv AT sarabolivar schwanncellroleinselectivityofnerveregeneration
AT xaviernavarro schwanncellroleinselectivityofnerveregeneration
AT estherudina schwanncellroleinselectivityofnerveregeneration