Skaper Stephen D
Department of Pharmacology and Anesthesiology, University of Padova, Padova, Italy.
Methods Mol Biol. 2012;846:1-12. doi: 10.1007/978-1-61779-536-7_1.
The neurotrophins are a family of closely related proteins that were first identified as survival factors for sympathetic and sensory neurons and have since been shown to control a number of aspects of survival, development, and function of neurons in both the central and peripheral nervous systems. Limiting quantities of neurotrophins during development control the numbers of surviving neurons to ensure a match between neurons and the requirement for a suitable density of target innervation. Biological effects of each of the four mammalian neurotrophins are mediated through activation of one or more of the three members of the tropomyosin-related kinase (Trk) family of receptor tyrosine kinases (TrkA, TrkB, and TrkC). In addition, all neurotrophins activate the p75 neurotrophin receptor, a member of the tumor necrosis factor receptor superfamily. Neurotrophin engagement of Trk receptors leads to activation of Ras, phosphatidylinositol 3-kinase, phospholipase C-γ1, and signaling pathways controlled through these proteins, including the mitogen-activated protein kinases. Neurotrophin availability is required into adulthood, where they control synaptic function and plasticity and sustain neuronal cell survival, morphology, and differentiation. This chapter will provide an overview of neurotrophin biology, their receptors, and signaling pathways.
神经营养因子是一类密切相关的蛋白质家族,最初被鉴定为交感神经元和感觉神经元的存活因子,此后已证明它们可控制中枢和外周神经系统中神经元存活、发育和功能的多个方面。发育过程中有限数量的神经营养因子控制着存活神经元的数量,以确保神经元与合适密度的靶标神经支配需求相匹配。四种哺乳动物神经营养因子中的每一种的生物学效应都是通过激活原肌球蛋白相关激酶(Trk)家族受体酪氨酸激酶(TrkA、TrkB和TrkC)的三个成员中的一个或多个来介导的。此外,所有神经营养因子都会激活p75神经营养因子受体,它是肿瘤坏死因子受体超家族的成员。神经营养因子与Trk受体的结合会导致Ras、磷脂酰肌醇3激酶、磷脂酶C-γ1以及通过这些蛋白质控制的信号通路激活,包括丝裂原活化蛋白激酶。成年期也需要神经营养因子,它们在成年期控制突触功能和可塑性,并维持神经元细胞的存活、形态和分化。本章将概述神经营养因子生物学、它们的受体和信号通路。