CRMP2 and CRMP4 Are Differentially Required for Axon Guidance and Growth in Zebrafish Retinal Neurons

Axons are directed to their correct targets by guidance cues during neurodevelopment. Many axon guidance cues have been discovered; however, much less known is about how the growth cones transduce the extracellular guidance cues to intracellular responses. Collapsin response mediator proteins (CRMPs...

Full description

Saved in:
Bibliographic Details
Main Authors: Zhi-Zhi Liu, Jian Zhu, Chang-Ling Wang, Xin Wang, Ying-Ying Han, Ling-Yan Liu, Hong A. Xu
Format: Article
Language:English
Published: Wiley 2018-01-01
Series:Neural Plasticity
Online Access:http://dx.doi.org/10.1155/2018/8791304
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1832554285850689536
author Zhi-Zhi Liu
Jian Zhu
Chang-Ling Wang
Xin Wang
Ying-Ying Han
Ling-Yan Liu
Hong A. Xu
author_facet Zhi-Zhi Liu
Jian Zhu
Chang-Ling Wang
Xin Wang
Ying-Ying Han
Ling-Yan Liu
Hong A. Xu
author_sort Zhi-Zhi Liu
collection DOAJ
description Axons are directed to their correct targets by guidance cues during neurodevelopment. Many axon guidance cues have been discovered; however, much less known is about how the growth cones transduce the extracellular guidance cues to intracellular responses. Collapsin response mediator proteins (CRMPs) are a family of intracellular proteins that have been found to mediate growth cone behavior in vitro; however, their roles in vivo in axon development are much less explored. In zebrafish embryos, we find that CRMP2 and CRMP4 are expressed in the retinal ganglion cell layer when retinal axons are crossing the midline. Knocking down CRMP2 causes reduced elongation and premature termination of the retinal axons, while knocking down CRMP4 results in ipsilateral misprojections of retinal axons that would normally project to the contralateral brain. Furthermore, CRMP4 synchronizes with neuropilin 1 in retinal axon guidance, suggesting that CRMP4 might mediate the semaphorin/neuropilin signaling pathway. These results demonstrate that CRMP2 and CRMP4 function differentially in axon development in vivo.
format Article
id doaj-art-635ef42a10e84249864851761062c1fd
institution Kabale University
issn 2090-5904
1687-5443
language English
publishDate 2018-01-01
publisher Wiley
record_format Article
series Neural Plasticity
spelling doaj-art-635ef42a10e84249864851761062c1fd2025-02-03T05:51:56ZengWileyNeural Plasticity2090-59041687-54432018-01-01201810.1155/2018/87913048791304CRMP2 and CRMP4 Are Differentially Required for Axon Guidance and Growth in Zebrafish Retinal NeuronsZhi-Zhi Liu0Jian Zhu1Chang-Ling Wang2Xin Wang3Ying-Ying Han4Ling-Yan Liu5Hong A. Xu6Institute of Life Science, Nanchang University, Nanchang, ChinaInstitute of Life Science, Nanchang University, Nanchang, ChinaInstitute of Life Science, Nanchang University, Nanchang, ChinaInstitute of Life Science, Nanchang University, Nanchang, ChinaInstitute of Life Science, Nanchang University, Nanchang, ChinaInstitute of Life Science, Nanchang University, Nanchang, ChinaInstitute of Life Science, Nanchang University, Nanchang, ChinaAxons are directed to their correct targets by guidance cues during neurodevelopment. Many axon guidance cues have been discovered; however, much less known is about how the growth cones transduce the extracellular guidance cues to intracellular responses. Collapsin response mediator proteins (CRMPs) are a family of intracellular proteins that have been found to mediate growth cone behavior in vitro; however, their roles in vivo in axon development are much less explored. In zebrafish embryos, we find that CRMP2 and CRMP4 are expressed in the retinal ganglion cell layer when retinal axons are crossing the midline. Knocking down CRMP2 causes reduced elongation and premature termination of the retinal axons, while knocking down CRMP4 results in ipsilateral misprojections of retinal axons that would normally project to the contralateral brain. Furthermore, CRMP4 synchronizes with neuropilin 1 in retinal axon guidance, suggesting that CRMP4 might mediate the semaphorin/neuropilin signaling pathway. These results demonstrate that CRMP2 and CRMP4 function differentially in axon development in vivo.http://dx.doi.org/10.1155/2018/8791304
spellingShingle Zhi-Zhi Liu
Jian Zhu
Chang-Ling Wang
Xin Wang
Ying-Ying Han
Ling-Yan Liu
Hong A. Xu
CRMP2 and CRMP4 Are Differentially Required for Axon Guidance and Growth in Zebrafish Retinal Neurons
Neural Plasticity
title CRMP2 and CRMP4 Are Differentially Required for Axon Guidance and Growth in Zebrafish Retinal Neurons
title_full CRMP2 and CRMP4 Are Differentially Required for Axon Guidance and Growth in Zebrafish Retinal Neurons
title_fullStr CRMP2 and CRMP4 Are Differentially Required for Axon Guidance and Growth in Zebrafish Retinal Neurons
title_full_unstemmed CRMP2 and CRMP4 Are Differentially Required for Axon Guidance and Growth in Zebrafish Retinal Neurons
title_short CRMP2 and CRMP4 Are Differentially Required for Axon Guidance and Growth in Zebrafish Retinal Neurons
title_sort crmp2 and crmp4 are differentially required for axon guidance and growth in zebrafish retinal neurons
url http://dx.doi.org/10.1155/2018/8791304
work_keys_str_mv AT zhizhiliu crmp2andcrmp4aredifferentiallyrequiredforaxonguidanceandgrowthinzebrafishretinalneurons
AT jianzhu crmp2andcrmp4aredifferentiallyrequiredforaxonguidanceandgrowthinzebrafishretinalneurons
AT changlingwang crmp2andcrmp4aredifferentiallyrequiredforaxonguidanceandgrowthinzebrafishretinalneurons
AT xinwang crmp2andcrmp4aredifferentiallyrequiredforaxonguidanceandgrowthinzebrafishretinalneurons
AT yingyinghan crmp2andcrmp4aredifferentiallyrequiredforaxonguidanceandgrowthinzebrafishretinalneurons
AT lingyanliu crmp2andcrmp4aredifferentiallyrequiredforaxonguidanceandgrowthinzebrafishretinalneurons
AT hongaxu crmp2andcrmp4aredifferentiallyrequiredforaxonguidanceandgrowthinzebrafishretinalneurons