Ernsberger Uwe
Interdisciplinary Center for Neurosciences (IZN), INF 307, University of Heidelberg, 69120, Heidelberg, Germany.
Cell Tissue Res. 2009 Jun;336(3):349-84. doi: 10.1007/s00441-009-0784-z. Epub 2009 Apr 23.
Manipulation of neurotrophin (NT) signalling by administration or depletion of NTs, by transgenic overexpression or by deletion of genes coding for NTs and their receptors has demonstrated the importance of NT signalling for the survival and differentiation of neurons in sympathetic and dorsal root ganglia (DRG). Combination with mutation of the proapoptotic Bax gene allows the separation of survival and differentiation effects. These studies together with cell culture analysis suggest that NT signalling directly regulates the differentiation of neuron subpopulations and their integration into neural networks. The high-affinity NT receptors trkA, trkB and trkC are restricted to subpopulations of mature neurons, whereas their expression at early developmental stages largely overlaps. trkC is expressed throughout sympathetic ganglia and DRG early after ganglion formation but becomes restricted to small neuron subpopulations during embryogenesis when trkA is turned on. The temporal relationship between trkA and trkC expression is conserved between sympathetic ganglia and DRG. In DRG, NGF signalling is required not only for survival, but also for the differentiation of nociceptors. Expression of neuropeptides calcitonin gene-related peptide and substance P, which specify peptidergic nociceptors, depends on nerve growth factor (NGF) signalling. ret expression indicative of non-peptidergic nociceptors is also promoted by the NGF-signalling pathway. Regulation of TRP channels by NGF signalling might specify the temperature sensitivity of afferent neurons embryonically. The manipulation of NGF levels "tunes" heat sensitivity in nociceptors at postnatal and adult stages. Brain-derived neurotrophic factor signalling is required for subpopulations of DRG neurons that are not fully characterized; it affects mechanical sensitivity in slowly adapting, low-threshold mechanoreceptors and might involve the regulation of DEG/ENaC ion channels. NT3 signalling is required for the generation and survival of various DRG neuron classes, in particular proprioceptors. Its importance for peripheral projections and central connectivity of proprioceptors demonstrates the significance of NT signalling for integrating responsive neurons in neural networks. The molecular targets of NT3 signalling in proprioceptor differentiation remain to be characterized. In sympathetic ganglia, NGF signalling regulates dendritic development and axonal projections. Its role in the specification of other neuronal properties is less well analysed. In vitro analysis suggests the involvement of NT signalling in the choice between the noradrenergic and cholinergic transmitter phenotype, in the expression of various classes of ion channels and for target connectivity. In vivo analysis is required to show the degree to which NT signalling regulates these sympathetic neuron properties in developing embryos and postnatally.
通过给予或消耗神经营养因子(NT)、转基因过表达或缺失编码NT及其受体的基因来操纵NT信号,已证明NT信号对于交感神经节和背根神经节(DRG)中神经元的存活和分化至关重要。与促凋亡Bax基因突变相结合,可以分离存活和分化效应。这些研究以及细胞培养分析表明,NT信号直接调节神经元亚群的分化及其融入神经网络的过程。高亲和力NT受体trkA、trkB和trkC仅限于成熟神经元的亚群,而它们在发育早期阶段的表达在很大程度上是重叠的。trkC在神经节形成后早期在整个交感神经节和DRG中表达,但在胚胎发育过程中,当trkA开启时,它会局限于小神经元亚群。trkA和trkC表达之间的时间关系在交感神经节和DRG之间是保守的。在DRG中,NGF信号不仅对伤害感受器的存活是必需的,而且对其分化也是必需的。指定肽能伤害感受器的神经肽降钙素基因相关肽和P物质的表达取决于神经生长因子(NGF)信号。指示非肽能伤害感受器的ret表达也由NGF信号通路促进。NGF信号对TRP通道的调节可能在胚胎期确定传入神经元的温度敏感性。在出生后和成年阶段,NGF水平的操纵可“调节”伤害感受器的热敏感性。脑源性神经营养因子信号对于尚未完全表征的DRG神经元亚群是必需的;它影响慢适应、低阈值机械感受器的机械敏感性,并且可能涉及对DEG/ENaC离子通道的调节。NT3信号对于各种DRG神经元类型的产生和存活是必需的,特别是本体感受器。它对本体感受器外周投射和中枢连接的重要性证明了NT信号对于将反应性神经元整合到神经网络中的意义。NT3信号在本体感受器分化中的分子靶点仍有待确定。在交感神经节中,NGF信号调节树突发育和轴突投射。其在确定其他神经元特性方面的作用分析较少。体外分析表明,NT信号参与去甲肾上腺素能和胆碱能递质表型的选择、各类离子通道的表达以及靶连接。需要进行体内分析以显示NT信号在发育中的胚胎和出生后调节这些交感神经元特性的程度。