Understanding Proneurotrophin Actions: Recent Advances and Challenges

被引:140
|
作者
Teng, Kenneth K. [1 ]
Felice, Sarah [1 ]
Kim, Taeho [1 ]
Hempstead, Barbara L. [1 ]
机构
[1] Weill Cornell Med Coll, Dept Med, New York, NY 10065 USA
关键词
ProNGF; ProBDNF; neurodegenerative diseases; neural development; neuronal apoptosis; NERVE GROWTH-FACTOR; P75 NEUROTROPHIN RECEPTOR; LONG-TERM DEPRESSION; CELL-DEATH; NEURONAL APOPTOSIS; HIGH-AFFINITY; SYMPATHETIC NEURONS; HIPPOCAMPAL-NEURONS; PRO-BDNF; SIGNAL-TRANSDUCTION;
D O I
10.1002/dneu.20768
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Neurotrophins are initially synthesized as larger precursors (proneurotrophins), which undergo proteolytic cleavage to yield mature forms. Although the functions of the mature neurotrophins have been well established during neural development and in the adult nervous system, roles for the proneurotrophins in developmental and injury-induced cell death, as well as in synaptic plasticity, have only recently been appreciated. Interestingly, both mature neurotrophins and proneurotrophins utilize dual-receptor complexes to mediate their actions. The mature neurotrophin coreceptors consist of the Trk receptor tyrosine kinases and p75(NTR), wherein Trk transduces survival and differentiative signaling, and p75(NTR) modulates the affinity and selectivity of Trk activation. On the other hand, proneurotrophins engage p75(NTR) and the structurally distinct coreceptor sortilin, to initiate p75(NTR)-dependent signal transduction cascade. Although the specificity of mature neurotrophins vs. proneurotrophins actions is due in part to the formation of distinct coreceptor complexes, a,number of recent studies highlight how different p75(NTR)-mediated cellular actions are modulated. Here, we review emerging evidence for a novel transmembrane mechanism for ligand-specific p75(NTR) activation and several mechanisms by which p75(NTR)-dependent apoptotic and nonapoptotic responses can be selective activated. (C) 2010 Wiley Periodicals. Inc. Develop Neurobiol 70: 350-359, 2010
引用
收藏
页码:350 / 359
页数:10
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