Literature DB >> 25830493

Differential motor and sensory functional recovery in male but not female adult rats is associated with remyelination rather than axon regeneration after sciatic nerve crush.

Ling-Ling Tong1, You-Quan Ding, Hong-Bo Jing, Xuan-Yang Li, Jian-Guo Qi.   

Abstract

Peripheral nerve functional recovery after injuries relies on both axon regeneration and remyelination. Both axon regeneration and remyelination require intimate interactions between regenerating neurons and their accompanying Schwann cells. Previous studies have shown that motor and sensory neurons are intrinsically different in their regeneration potentials. Moreover, denervated Schwann cells accompanying myelinated motor and sensory axons have distinct gene expression profiles for regeneration-associated growth factors. However, it is unknown whether differential motor and sensory functional recovery exists. If so, the particular one among axon regeneration and remyelination responsible for this difference remains unclear. Here, we aimed to establish an adult rat sciatic nerve crush model with the nonserrated microneedle holders and measured rat motor and sensory functions during regeneration. Furthermore, axon regeneration and remyelination was evaluated by morphometric analysis of electron microscopic images on the basis of nerve fiber classification. Our results showed that Aα fiber-mediated motor function was successfully recovered in both male and female rats. Aδ fiber-mediated sensory function was partially restored in male rats, but completely recovered in female littermates. For both male and female rats, the numbers of regenerated motor and sensory axons were quite comparable. However, remyelination was diverse among myelinated motor and sensory nerve fibers. In detail, Aβ and Aδ fibers incompletely remyelinated in male, but not female rats, whereas Aα fibers fully remyelinated in both sexes. Our result indicated that differential motor and sensory functional recovery in male but not female adult rats is associated with remyelination rather than axon regeneration after sciatic nerve crush.

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Year:  2015        PMID: 25830493     DOI: 10.1097/WNR.0000000000000366

Source DB:  PubMed          Journal:  Neuroreport        ISSN: 0959-4965            Impact factor:   1.837


  4 in total

1.  Modest enhancement of sensory axon regeneration in the sciatic nerve with conditional co-deletion of PTEN and SOCS3 in the dorsal root ganglia of adult mice.

Authors:  Zachary R Gallaher; Oswald Steward
Journal:  Exp Neurol       Date:  2018-02-16       Impact factor: 5.330

2.  Differences in the Structure and Protein Expression of Femoral Nerve Branches in Rats.

Authors:  Shuai Wei; Qian Hu; Xiaoqing Cheng; Jianxiong Ma; Xuezhen Liang; Jiang Peng; Wenjing Xu; Xun Sun; Gonghai Han; Xinlong Ma; Yu Wang
Journal:  Front Neuroanat       Date:  2020-04-08       Impact factor: 3.856

Review 3.  The Effect of Schwann Cells/Schwann Cell-Like Cells on Cell Therapy for Peripheral Neuropathy.

Authors:  Qian Wang; Fang-Yu Chen; Zhuo-Min Ling; Wen-Feng Su; Ya-Yu Zhao; Gang Chen; Zhong-Ya Wei
Journal:  Front Cell Neurosci       Date:  2022-03-08       Impact factor: 5.505

Review 4.  Therapeutic Low-Intensity Ultrasound for Peripheral Nerve Regeneration - A Schwann Cell Perspective.

Authors:  Jenica Acheta; Shannon B Z Stephens; Sophie Belin; Yannick Poitelon
Journal:  Front Cell Neurosci       Date:  2022-01-05       Impact factor: 6.147

  4 in total

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