Involvement of Akt in neurite outgrowth

被引:200
作者
Read, Danielle E. [1 ,2 ]
Gorman, Adrienne M. [1 ,2 ]
机构
[1] Natl Univ Ireland, Natl Ctr Biomed Engn Sci, Galway, Ireland
[2] Natl Univ Ireland, Sch Nat Sci, Dept Biochem, Cell Death & Survival Grp, Galway, Ireland
关键词
Akt; Differentiation; Glycogen synthase kinase 3 beta; Heat shock protein 27 (Hsp27); Neurite outgrowth; PROTEIN-KINASE-B; NF-KAPPA-B; NERVE GROWTH-FACTOR; HEAT-SHOCK-PROTEIN; ADULT SENSORY NEURONS; RICTOR-MTOR COMPLEX; PC12; CELLS; PHOSPHATIDYLINOSITOL; 3-KINASE; SIGNALING PATHWAY; PHOSPHOINOSITIDE;
D O I
10.1007/s00018-009-0057-8
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
The regulation of neuronal differentiation and neurite outgrowth is essential during development of the nervous system and is crucial in developing therapies to promote axon regeneration after nerve injury or in neurodegenerative diseases. The serine/threonine kinase Akt has been well documented to promote neuronal survival. More recently Akt has also been revealed as key mediator of several aspects of neurite outgrowth, including elongation, branching and calibre. Downstream of Akt, several substrates have been identified that are likely to play key roles in Akt-mediated neurite outgrowth, such as glycogen synthase kinase 3 beta, peripherin, mammalian target of rapamycin and delta-catenin. The physical interaction between Akt and Hsp27, another protein that has been linked with neurite outgrowth, may also be significant in the process of neurite outgrowth. This review will unite and discuss the research to date that has examined the functionality of Akt in neuronal differentiation during development and neurite outgrowth.
引用
收藏
页码:2975 / 2984
页数:10
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