Dechant G
Department of Neurobiochemistry, Max Planck Institute of Neurobiology, Martinsried, Germany.
Cell Tissue Res. 2001 Aug;305(2):229-38. doi: 10.1007/s004410100378.
Neurotrophins signal via a dual-receptor system comprising receptor tyrosine kinases, the Trks, and a tumor necrosis factor (TNF) receptor like molecule, p75. Interest in these receptors was spurred on by the finding that they are employed by their neurotrophin ligands to activate opposing cellular mechanisms. Signalling via Trk receptors promotes the survival of embryonic neurons, whereas activation of p75 can trigger apoptosis. However, this antagonistic view is an oversimplification. It is more accurate to refer to this system as a signalling network in which ligands, receptors and their intracellular target proteins are linked by balanced biochemical interactions. This article reviews recent advances in our understanding of these molecular mechanisms which critically determine many cell-type-specific responses to neurotrophins. Emphasis is given to the formation of receptor complexes, the generation of receptor diversity by alternative splicing and the influence exerted by the local membrane environment on neurotrophin signalling.
神经营养因子通过一个双受体系统进行信号传导,该系统由受体酪氨酸激酶(Trks)和一个肿瘤坏死因子(TNF)受体样分子p75组成。这些受体之所以受到关注,是因为研究发现它们被其神经营养因子配体用于激活相反的细胞机制。通过Trk受体进行信号传导可促进胚胎神经元的存活,而p75的激活则可触发细胞凋亡。然而,这种拮抗观点过于简单化。更准确地说,这个系统是一个信号网络,其中配体、受体及其细胞内靶蛋白通过平衡的生化相互作用联系在一起。本文综述了我们对这些分子机制理解的最新进展,这些机制决定性地决定了许多细胞类型对神经营养因子的特异性反应。重点介绍了受体复合物的形成、通过可变剪接产生的受体多样性以及局部膜环境对神经营养因子信号传导的影响。