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JNK Signaling Pathway Involvement in Spinal Cord Neuron Development and Death.
Schellino, Roberta; Boido, Marina; Vercelli, Alessandro.
Afiliación
  • Schellino R; Department of Neuroscience Rita Levi Montalcini, University of Turin, 10126 Turin, Italy.
  • Boido M; Neuroscience Institute Cavalieri Ottolenghi, University of Turin, 10043 Orbassano (TO), Italy.
  • Vercelli A; Department of Neuroscience Rita Levi Montalcini, University of Turin, 10126 Turin, Italy.
Cells ; 8(12)2019 12 05.
Article en En | MEDLINE | ID: mdl-31817379
ABSTRACT
The c-Jun NH2-terminal protein kinase (JNK) is a Janus-faced kinase, which, in the nervous system, plays important roles in a broad range of physiological and pathological processes. Three genes, encoding for 10 JNK isoforms, have been identified jnk1, jnk2, and jnk3. In the developing spinal cord, JNK proteins control neuronal polarity, axon growth/pathfinding, and programmed cell death; in adulthood they can drive degeneration and regeneration, after pathological insults. Indeed, recent studies have highlighted a role for JNK in motor neuron (MN) diseases, such as amyotrophic lateral sclerosis and spinal muscular atrophy. In this review we discuss how JNK-dependent signaling regulates apparently contradictory functions in the spinal cord, in both the developmental and adult stages. In addition, we examine the evidence that the specific targeting of JNK signaling pathway may represent a promising therapeutic strategy for the treatment of MN diseases.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Médula Espinal / Sistema de Señalización de MAP Quinasas / Proteínas Quinasas JNK Activadas por Mitógenos / Neuronas Tipo de estudio: Etiology_studies Límite: Animals / Humans Idioma: En Revista: Cells Año: 2019 Tipo del documento: Article País de afiliación: Italia

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Médula Espinal / Sistema de Señalización de MAP Quinasas / Proteínas Quinasas JNK Activadas por Mitógenos / Neuronas Tipo de estudio: Etiology_studies Límite: Animals / Humans Idioma: En Revista: Cells Año: 2019 Tipo del documento: Article País de afiliación: Italia