Ginty David D, Segal Rosalind A
Department of Neuroscience and Howard Hughes Medical Institute, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205-2185, USA.
Curr Opin Neurobiol. 2002 Jun;12(3):268-74. doi: 10.1016/s0959-4388(02)00326-4.
Target-derived neurotrophins are required for the growth and survival of innervating neurons. When released by postsynaptic targets, neurotrophins bind receptors (Trks) on nerve terminals. Activated Trks signal locally within distal axons and retrogradely through long axons to distant cell bodies in order to promote gene expression and survival. Although the mechanism of retrograde neurotrophin signaling is not fully elucidated, considerable evidence supports a model in which the vesicular transport of neurotrophin-Trk complexes transmits a survival signal that involves PI3K and Erk5. Other, non-vesicular modes of retrograde signaling are likely to function in parallel. Recent studies highlight the importance of the location of stimulation as a determinant of Trk signaling. Defects in signaling from distal axons to cell bodies may be causally related to neurodegenerative disorders.
靶源性神经营养因子是支配性神经元生长和存活所必需的。当神经营养因子由突触后靶释放时,它们会与神经末梢上的受体(Trks)结合。激活的Trks在远端轴突内进行局部信号传导,并通过长轴突逆行传导至远处的细胞体,以促进基因表达和细胞存活。尽管逆行神经营养因子信号传导的机制尚未完全阐明,但大量证据支持一种模型,即神经营养因子-Trk复合物的囊泡运输传递了一个涉及PI3K和Erk5的存活信号。其他非囊泡性逆行信号传导模式可能并行发挥作用。最近的研究强调了刺激位置作为Trk信号传导决定因素的重要性。从远端轴突到细胞体的信号传导缺陷可能与神经退行性疾病存在因果关系。