The Dyslexia-susceptibility protein KIAA0319 inhibits axon growth through Smad2 signaling
| Autor: | Franquinho, F, Nogueira-Rodrigues, J, Duarte, J, Esteves, S, Carter-Su, C, Monaco, A, Molnár, Z, Velayos-Baeza, A, Brites, P, Sousa, M |
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| Jazyk: | angličtina |
| Rok vydání: | 2017 |
| Předmět: |
Male
Aging Neuronal Outgrowth Mice Transgenic Nerve Tissue Proteins Smad2 Protein Cell Enlargement Hippocampus Cell Line Protein Domains Ganglia Spinal axon growth dyslexia KIAA0319 Animals Humans Rats Wistar Cells Cultured Neurons axon regeneration Original Articles Janus Kinase 2 Sciatic Nerve Axons Nerve Regeneration Mice Inbred C57BL Spinal Cord nervous system Female Cell Adhesion Molecules Smad2 |
| Zdroj: | Cerebral Cortex (New York, NY) |
| ISSN: | 1460-2199 1047-3211 |
| Popis: | 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. |
| Databáze: | OpenAIRE |
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