Nykjaer Anders, Willnow Thomas E, Petersen Claus Munck
Department of Medical Biochemistry, Ole Worms Allé Building. 170, Aarhus University, DK-8000C Aarhus, Denmark.
Curr Opin Neurobiol. 2005 Feb;15(1):49-57. doi: 10.1016/j.conb.2005.01.004.
During neuronal development, neurotrophins are essential factors that promote survival, differentiation and myelination of neurons. The trophic signals are relayed to the cells via binding to Trk receptor tyrosine kinases and the p75 neurotrophin receptor. Paradoxically, the p75 neurotrophin receptor also ensures rapid and appropriate apoptosis of neonatal neurons not reaching their proper targets and transmits death signals to injured neurons. Until recently, the mechanisms by which the p75 neurotrophin receptor governs these opposing functions have remained elusive. By the identification of new ligands and cytosolic interacting partners, receptor cleavage products and coreceptors, some of these mechanisms are now being unraveled. Here, we review recent progress in delineating the molecular networks that enable p75(NTR) to dictate life and death.
在神经元发育过程中,神经营养因子是促进神经元存活、分化和髓鞘形成的关键因素。这些营养信号通过与Trk受体酪氨酸激酶和p75神经营养因子受体结合传递给细胞。矛盾的是,p75神经营养因子受体还能确保未到达合适靶点的新生神经元快速且适当地凋亡,并将死亡信号传递给受损神经元。直到最近,p75神经营养因子受体调控这些相反功能的机制仍不清楚。通过鉴定新的配体、胞质相互作用伴侣、受体裂解产物和共受体,其中一些机制现已被揭示。在此,我们综述了在描绘使p75(NTR)决定生死的分子网络方面的最新进展。