Zhong Jian
Biol Chem. 2016 Mar;397(3):215-22. doi: 10.1515/hsz-2015-0270.
In postmitotic neurons, the activation of RAS family small GTPases regulates survival, growth and differentiation. Dysregulation of RAS or its major effector pathway, the cascade of RAF-, mitogen-activated and extracellular-signal regulated kinase kinases (MEK), and extracellular-signal regulated kinases (ERK) causes the RASopathies, a group of neurodevelopmental disorders whose pathogenic mechanisms are the subject of intense research. I here summarize the functions of RAS-RAF-MEK-ERK signaling in neurons in vivo, and discuss perspectives for harnessing this pathway to enable novel treatments for nervous system injury, the RASopathies, and possibly other neurological conditions.
在有丝分裂后的神经元中,RAS家族小GTP酶的激活调节细胞存活、生长和分化。RAS或其主要效应途径(RAF、丝裂原活化和细胞外信号调节激酶激酶(MEK)以及细胞外信号调节激酶(ERK)的级联反应)失调会导致RAS病,这是一组神经发育障碍,其致病机制是深入研究的主题。我在此总结了RAS-RAF-MEK-ERK信号通路在体内神经元中的功能,并讨论了利用该途径为神经系统损伤、RAS病以及可能的其他神经疾病开发新治疗方法的前景。