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神经营养素及其后果。

PROneurotrophins and CONSequences.

机构信息

Center for Neuroscience and Cell Biology (CNC), University of Coimbra, Coimbra, Portugal.

Institute for Interdisciplinary Research, University of Coimbra, Coimbra, Portugal.

出版信息

Mol Neurobiol. 2018 Apr;55(4):2934-2951. doi: 10.1007/s12035-017-0505-7. Epub 2017 Apr 29.

DOI:10.1007/s12035-017-0505-7
PMID:28456935
Abstract

Proneurotrophins were initially thought to be simple inactive precursors, only responsible for promoting the folding of the mature domain and for the regulation of the neurotrophin secretory pathway. However, recent evidence shows that proneurotrophins can be secreted to the extracellular space, bind with high affinity to specific receptor complexes and induce activation of the apoptotic machinery with subsequent cell death of different neuronal populations. These pathways can be activated due to injury and to several neurodegenerative disorders, which promote proneurotrophin secretion to the extracellular space. In addition to neuropathology, extracellular proneurotrophins also play a pivotal role in many other cellular mechanisms in the nervous system. Proneurotrophins were shown to mediate synaptic plasticity, namely long-term depression in hippocampal neurons. They are also important in axonal development, and an increase of pro- to mature neurotrophin ratio has been described as a trigger of cell death. The conversion of proneurotrophins into the respective mature form is controlled by the action of several enzymes and regulators. The failure in this regulation is now considered one of the possible mechanisms responsible for pathological cell death associated to proneurotrophins. Here, we discuss the processes behind proneurotrophin action, with particular focus on proBDNF and proNGF and their regulatory pathways. Additionally, we review the most recent studies concerning proneurotrophin involvement in neuronal death, in several disease-associated states in the CNS and PNS, and discuss future avenues of investigation in the proneurotrophin field.

摘要

神经营养蛋白原最初被认为是简单的无活性前体,仅负责促进成熟结构域的折叠和神经生长因子分泌途径的调节。然而,最近的证据表明,神经营养蛋白原可以分泌到细胞外空间,与特定的受体复合物高亲和力结合,并诱导凋亡机制的激活,随后导致不同神经元群体的细胞死亡。这些途径可以由于损伤和几种神经退行性疾病而被激活,这些疾病促进神经营养蛋白原原向细胞外空间的分泌。除神经病理学外,细胞外神经营养蛋白原原在神经系统的许多其他细胞机制中也起着关键作用。神经营养蛋白原原被证明可以介导突触可塑性,即在海马神经元中长时程抑郁。它们在轴突发育中也很重要,并且已经描述了前体神经生长因子向成熟神经生长因子的比例增加作为细胞死亡的触发因素。神经营养蛋白原原转化为相应的成熟形式是由几种酶和调节剂的作用控制的。这种调节的失败现在被认为是与神经营养蛋白原原相关的病理性细胞死亡的可能机制之一。在这里,我们讨论了神经营养蛋白原原作用背后的过程,特别关注 proBDNF 和 proNGF 及其调节途径。此外,我们还回顾了最近关于神经营养蛋白原原参与中枢神经系统和周围神经系统几种与疾病相关状态下的神经元死亡的研究,并讨论了神经营养蛋白原原领域未来的研究方向。

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