The Neuregulin-Rac-MKK7 pathway regulates antagonistic c-jun/Krox20 expression in Schwann cell dedifferentiation.
Glia
; 61(6): 892-904, 2013 Jun.
Article
em En
| MEDLINE
| ID: mdl-23505039
ABSTRACT
Schwann cells respond to nerve injury by dedifferentiating into immature states and producing neurotrophic factors, two actions that facilitate successful regeneration of axons. Previous reports have implicated the Raf-ERK cascade and the expression of c-jun in these Schwann cell responses. Here we used cultured primary Schwann cells to demonstrate that active Rac1 GTPase (Rac) functions as a negative regulator of Schwann cell differentiation by upregulating c-jun and downregulating Krox20 through the MKK7-JNK pathway, but not through the Raf-ERK pathway. The activation of MKK7 and induction of c-jun in sciatic nerves after axotomy was blocked by Rac inhibition. Microarray experiments revealed that the expression of regeneration-associated genes, such as glial cell line-derived neurotrophic factor and p75 neurotrophin receptor, after nerve injury was dependent on Rac but not on ERK. Finally, the inhibition of ErbB2 signaling prevented MKK7 activation, c-jun induction, and Rac-dependent gene expression in sciatic nerve explant cultures. Taken together, our results indicate that the neuregulin-Rac-MKK7-JNK/c-jun pathway regulates Schwann cell dedifferentiation following nerve injury.
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Base de dados:
MEDLINE
Assunto principal:
Células de Schwann
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Proteínas Proto-Oncogênicas c-jun
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Neuregulina-1
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MAP Quinase Quinase 7
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Proteínas Proto-Oncogênicas c-akt
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Proteína 2 de Resposta de Crescimento Precoce
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Desdiferenciação Celular
Idioma:
En
Ano de publicação:
2013
Tipo de documento:
Article