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Comparative transcriptomic profiling of peripheral efferent and afferent nerve fibres at different developmental stages in mice

Peripheral nerve injury impairs motor and sensory function in humans, and its functional recovery largely depends on the axonal outgrowth required for the accurate reinnervation of appropriate targets. To better understand how motor and sensory nerve fibres select their terminal pathways, an unbiase...

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Autores principales: Wang, Hongkui, Zhou, Youlang, Cong, Meng, Zhang, Li, Gu, Xiaosong, Tang, Xin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6086926/
https://www.ncbi.nlm.nih.gov/pubmed/30097601
http://dx.doi.org/10.1038/s41598-018-30463-0
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author Wang, Hongkui
Zhou, Youlang
Cong, Meng
Zhang, Li
Gu, Xiaosong
Tang, Xin
author_facet Wang, Hongkui
Zhou, Youlang
Cong, Meng
Zhang, Li
Gu, Xiaosong
Tang, Xin
author_sort Wang, Hongkui
collection PubMed
description Peripheral nerve injury impairs motor and sensory function in humans, and its functional recovery largely depends on the axonal outgrowth required for the accurate reinnervation of appropriate targets. To better understand how motor and sensory nerve fibres select their terminal pathways, an unbiased cDNA microarray analysis was conducted to examine differential gene expression patterns in peripheral efferent and afferent fibres at different developmental stages in mice. Gene ontology (GO) and Kyoto Enrichment of Genes and Genomes (KEGG) analyses revealed common and distinct features of enrichment for differentially expressed genes during motor and sensory nerve fibre development. Ingenuity Pathway Analysis (IPA) further indicated that the key differentially expressed genes were associated with trans-synaptic neurexin-neuroligin signalling components and a variety of gamma-aminobutyric acid (GABA) receptors. The aim of this study was to generate a framework of gene networks regulated during motor and sensory neuron differentiation/maturation. These data may provide new clues regarding the underlying cellular and molecular mechanisms that determine the intrinsic capacity of neurons to regenerate after peripheral nerve injury. Our findings may thus facilitate further development of a potential intervention to manipulate the therapeutic efficiency of peripheral nerve repair in the clinic.
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spelling pubmed-60869262018-08-16 Comparative transcriptomic profiling of peripheral efferent and afferent nerve fibres at different developmental stages in mice Wang, Hongkui Zhou, Youlang Cong, Meng Zhang, Li Gu, Xiaosong Tang, Xin Sci Rep Article Peripheral nerve injury impairs motor and sensory function in humans, and its functional recovery largely depends on the axonal outgrowth required for the accurate reinnervation of appropriate targets. To better understand how motor and sensory nerve fibres select their terminal pathways, an unbiased cDNA microarray analysis was conducted to examine differential gene expression patterns in peripheral efferent and afferent fibres at different developmental stages in mice. Gene ontology (GO) and Kyoto Enrichment of Genes and Genomes (KEGG) analyses revealed common and distinct features of enrichment for differentially expressed genes during motor and sensory nerve fibre development. Ingenuity Pathway Analysis (IPA) further indicated that the key differentially expressed genes were associated with trans-synaptic neurexin-neuroligin signalling components and a variety of gamma-aminobutyric acid (GABA) receptors. The aim of this study was to generate a framework of gene networks regulated during motor and sensory neuron differentiation/maturation. These data may provide new clues regarding the underlying cellular and molecular mechanisms that determine the intrinsic capacity of neurons to regenerate after peripheral nerve injury. Our findings may thus facilitate further development of a potential intervention to manipulate the therapeutic efficiency of peripheral nerve repair in the clinic. Nature Publishing Group UK 2018-08-10 /pmc/articles/PMC6086926/ /pubmed/30097601 http://dx.doi.org/10.1038/s41598-018-30463-0 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Wang, Hongkui
Zhou, Youlang
Cong, Meng
Zhang, Li
Gu, Xiaosong
Tang, Xin
Comparative transcriptomic profiling of peripheral efferent and afferent nerve fibres at different developmental stages in mice
title Comparative transcriptomic profiling of peripheral efferent and afferent nerve fibres at different developmental stages in mice
title_full Comparative transcriptomic profiling of peripheral efferent and afferent nerve fibres at different developmental stages in mice
title_fullStr Comparative transcriptomic profiling of peripheral efferent and afferent nerve fibres at different developmental stages in mice
title_full_unstemmed Comparative transcriptomic profiling of peripheral efferent and afferent nerve fibres at different developmental stages in mice
title_short Comparative transcriptomic profiling of peripheral efferent and afferent nerve fibres at different developmental stages in mice
title_sort comparative transcriptomic profiling of peripheral efferent and afferent nerve fibres at different developmental stages in mice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6086926/
https://www.ncbi.nlm.nih.gov/pubmed/30097601
http://dx.doi.org/10.1038/s41598-018-30463-0
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