神经调节蛋白
生物
细胞生物学
雪旺细胞
神经调节蛋白1
MAPK/ERK通路
瓦勒氏变性
神经营养因子
坐骨神经损伤
神经营养素
轴突切开术
低亲和力神经生长因子受体
神经科学
再生(生物学)
信号转导
受体
遗传学
作者
Yoon Kyung Shin,So Young Jang,Joo Youn Park,So‐Young Park,Hye‐Jeong Lee,Duk Joon Suh,Hwan Tae Park
出处
期刊:Glia
[Wiley]
日期:2013-03-15
卷期号:61 (6): 892-904
被引量:45
摘要
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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