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The Dyslexia-susceptibility Protein KIAA0319 Inhibits Axon Growth Through Smad2 Signaling
KIAA0319 is a transmembrane protein associated with dyslexia with a presumed role in neuronal migration. Here we show that KIAA0319 expression is not restricted to the brain but also occurs in sensory and spinal cord neurons, increasing from early postnatal stages to adulthood and being downregulate...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5905272/ https://www.ncbi.nlm.nih.gov/pubmed/28334068 http://dx.doi.org/10.1093/cercor/bhx023 |
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author | Franquinho, Filipa Nogueira-Rodrigues, Joana Duarte, Joana M. Esteves, Sofia S. Carter-Su, Christin Monaco, Anthony P. Molnár, Zoltán Velayos-Baeza, Antonio Brites, Pedro Sousa, Mónica M. |
author_facet | Franquinho, Filipa Nogueira-Rodrigues, Joana Duarte, Joana M. Esteves, Sofia S. Carter-Su, Christin Monaco, Anthony P. Molnár, Zoltán Velayos-Baeza, Antonio Brites, Pedro Sousa, Mónica M. |
author_sort | Franquinho, Filipa |
collection | PubMed |
description | KIAA0319 is a transmembrane protein associated with dyslexia with a presumed role in neuronal migration. Here we show that KIAA0319 expression is not restricted to the brain but also occurs in sensory and spinal cord neurons, increasing from early postnatal stages to adulthood and being downregulated by injury. This suggested that KIAA0319 participates in functions unrelated to neuronal migration. Supporting this hypothesis, overexpression of KIAA0319 repressed axon growth in hippocampal and dorsal root ganglia neurons; the intracellular domain of KIAA0319 was sufficient to elicit this effect. A similar inhibitory effect was observed in vivo as axon regeneration was impaired after transduction of sensory neurons with KIAA0319. Conversely, the deletion of Kiaa0319 in neurons increased neurite outgrowth in vitro and improved axon regeneration in vivo. At the mechanistic level, KIAA0319 engaged the JAK2-SH2B1 pathway to activate Smad2, which played a central role in KIAA0319-mediated repression of axon growth. In summary, we establish KIAA0319 as a novel player in axon growth and regeneration with the ability to repress the intrinsic growth potential of axons. This study describes a novel regulatory mechanism operating during peripheral nervous system and central nervous system axon growth, and offers novel targets for the development of effective therapies to promote axon regeneration. |
format | Online Article Text |
id | pubmed-5905272 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-59052722018-04-24 The Dyslexia-susceptibility Protein KIAA0319 Inhibits Axon Growth Through Smad2 Signaling Franquinho, Filipa Nogueira-Rodrigues, Joana Duarte, Joana M. Esteves, Sofia S. Carter-Su, Christin Monaco, Anthony P. Molnár, Zoltán Velayos-Baeza, Antonio Brites, Pedro Sousa, Mónica M. Cereb Cortex Original Articles KIAA0319 is a transmembrane protein associated with dyslexia with a presumed role in neuronal migration. Here we show that KIAA0319 expression is not restricted to the brain but also occurs in sensory and spinal cord neurons, increasing from early postnatal stages to adulthood and being downregulated by injury. This suggested that KIAA0319 participates in functions unrelated to neuronal migration. Supporting this hypothesis, overexpression of KIAA0319 repressed axon growth in hippocampal and dorsal root ganglia neurons; the intracellular domain of KIAA0319 was sufficient to elicit this effect. A similar inhibitory effect was observed in vivo as axon regeneration was impaired after transduction of sensory neurons with KIAA0319. Conversely, the deletion of Kiaa0319 in neurons increased neurite outgrowth in vitro and improved axon regeneration in vivo. At the mechanistic level, KIAA0319 engaged the JAK2-SH2B1 pathway to activate Smad2, which played a central role in KIAA0319-mediated repression of axon growth. In summary, we establish KIAA0319 as a novel player in axon growth and regeneration with the ability to repress the intrinsic growth potential of axons. This study describes a novel regulatory mechanism operating during peripheral nervous system and central nervous system axon growth, and offers novel targets for the development of effective therapies to promote axon regeneration. Oxford University Press 2017-03 2017-02-17 /pmc/articles/PMC5905272/ /pubmed/28334068 http://dx.doi.org/10.1093/cercor/bhx023 Text en © The Author 2017. Published by Oxford University Press. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles Franquinho, Filipa Nogueira-Rodrigues, Joana Duarte, Joana M. Esteves, Sofia S. Carter-Su, Christin Monaco, Anthony P. Molnár, Zoltán Velayos-Baeza, Antonio Brites, Pedro Sousa, Mónica M. The Dyslexia-susceptibility Protein KIAA0319 Inhibits Axon Growth Through Smad2 Signaling |
title | The Dyslexia-susceptibility Protein KIAA0319 Inhibits Axon Growth Through Smad2 Signaling |
title_full | The Dyslexia-susceptibility Protein KIAA0319 Inhibits Axon Growth Through Smad2 Signaling |
title_fullStr | The Dyslexia-susceptibility Protein KIAA0319 Inhibits Axon Growth Through Smad2 Signaling |
title_full_unstemmed | The Dyslexia-susceptibility Protein KIAA0319 Inhibits Axon Growth Through Smad2 Signaling |
title_short | The Dyslexia-susceptibility Protein KIAA0319 Inhibits Axon Growth Through Smad2 Signaling |
title_sort | dyslexia-susceptibility protein kiaa0319 inhibits axon growth through smad2 signaling |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5905272/ https://www.ncbi.nlm.nih.gov/pubmed/28334068 http://dx.doi.org/10.1093/cercor/bhx023 |
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