Chondroitin Sulfate Impairs Neural Stem Cell Migration Through ROCK Activation

Brain injuries such as trauma and stroke lead to glial scar formation by reactive astrocytes which produce and secret axonal outgrowth inhibitors. Chondroitin sulfate proteoglycans (CSPG) constitute a well-known class of extracellular matrix molecules produced at the glial scar and cause growth cone...

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Detalles Bibliográficos
Autores: Galindo, Layla Testa [UNIFESP], Mundim, Mayara T. V. V. [UNIFESP], Pinto, Agnes S. [UNIFESP], Chiarantin, Gabrielly Maria Denadai [UNIFESP], Almeida, Maira E. S., Lamers, Marcelo L., Horwitz, Alan R., Santos, Marinilce F., Porcionatto, Marimélia Aparecida [UNIFESP]
Tipo de recurso: artículo
Estado:Versión publicada
Fecha de publicación:2018
País:Brasil
Institución:Universidade Federal de São Paulo (UNIFESP)
Repositorio:Repositório Institucional da UNIFESP
Idioma:inglés
OAI Identifier:oai:repositorio.unifesp.br:11600/55794
Acceso en línea:http://dx.doi.org/10.1007/s12035-017-0565-8
https://repositorio.unifesp.br/handle/11600/55794
Access Level:acceso abierto
Palabra clave:Neural stem cell
Cell migration
Chondroitin sulfate
Traumatic brain injury
RhoA
Rock
Descripción
Sumario:Brain injuries such as trauma and stroke lead to glial scar formation by reactive astrocytes which produce and secret axonal outgrowth inhibitors. Chondroitin sulfate proteoglycans (CSPG) constitute a well-known class of extracellular matrix molecules produced at the glial scar and cause growth cone collapse. The CSPG glycosaminoglycan side chains composed of chondroitin sulfate (CS) are responsible for its inhibitory activity on neurite outgrowth and are dependent on RhoA activation. Here, we hypothesize that CSPG also impairs neural stem cell migration inhibiting their penetration into an injury site. We show that DCX+ neuroblasts do not penetrate a CSPG-rich injured area probably due to Nogo receptor activation and RhoA/ROCK signaling pathway as we demonstrate in vitro with neural stem cells cultured as neurospheres and pull-down for RhoA. Furthermore, CS-impaired cell migration in vitro induced the formation of large mature adhesions and altered cell protrusion dynamics. ROCK inhibition restored migration in vitro as well as decreased adhesion size.