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DSCAM Mutation Impairs Motor Cortex Network Dynamic and Voluntary Motor Functions.
Laflamme, Olivier D; Lemieux, Maxime; Thiry, Louise; Bretzner, Frédéric.
Afiliación
  • Laflamme OD; Centre de recherche du Centre Hospitalier Universitaire (CHU) de Québec, CHUL, 2705 Boul. Laurier, Québec, Canada.
  • Lemieux M; Centre de recherche du Centre Hospitalier Universitaire (CHU) de Québec, CHUL, 2705 Boul. Laurier, Québec, Canada.
  • Thiry L; Centre de recherche du Centre Hospitalier Universitaire (CHU) de Québec, CHUL, 2705 Boul. Laurier, Québec, Canada.
  • Bretzner F; Centre de recherche du Centre Hospitalier Universitaire (CHU) de Québec, CHUL, 2705 Boul. Laurier, Québec, Canada.
Cereb Cortex ; 29(6): 2313-2330, 2019 06 01.
Article en En | MEDLINE | ID: mdl-29718256
While it is well known that netrin-1 and its receptors UNC5 and UNC40 family members are involved in the normal establishment of the motor cortex and its corticospinal tract, less is known about its other receptor Down syndrome cell adherence molecule (DSCAM). DSCAM is expressed in the developing motor cortex, regulates axonal outgrowth of cortical neurons, and its mutation impairs the dendritic arborization of cortical neurons, thus suggesting that it might be involved in the normal development and functioning of the motor cortex. In comparison to WT littermates, DSCAM2J mutant mice slipped and misplaced their paw while walking on the rungs of a horizontal ladder, and exhibited more difficulties in stepping over an obstacle while walking at slow speed. Anterograde tracing showed a normal pyramidal decussation and corticospinal projection, but a more dorsal distribution of their axonal terminals in the spinal gray matter. Intracortical microstimulations showed a reduced corticospinal and intracortical efficacy, whereas stimulations of the pyramidal tract revealed a normal spinal efficacy and excitability of corticospinal tract axons, thus arguing for a dysfunctional cortical development. Our study reveals impairment of the network dynamics within the motor cortex, reducing corticospinal drive and impairing voluntary locomotor functions upon DSCAM2J mutation.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Tractos Piramidales / Moléculas de Adhesión Celular / Locomoción / Corteza Motora Límite: Animals Idioma: En Revista: Cereb Cortex Asunto de la revista: CEREBRO Año: 2019 Tipo del documento: Article País de afiliación: Canadá Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Tractos Piramidales / Moléculas de Adhesión Celular / Locomoción / Corteza Motora Límite: Animals Idioma: En Revista: Cereb Cortex Asunto de la revista: CEREBRO Año: 2019 Tipo del documento: Article País de afiliación: Canadá Pais de publicación: Estados Unidos