Neuregulins: subcellular localization, signaling pathways and their relationship with neuroplasticity and neurological diseases

M. Longart, Christian Calderón, Manuel González, María Elena Grela, J. Martínez
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Abstract

Neuregulins (NRGs) and their cognate ErbB receptors (ErbB2–ErbB4) constitute a vast group of proteins encoded by six different genes (NRG1–6) and many isoforms with critical roles in the development and functioning of the nervous system. NRGs are known to regulate important processes in the nervous system like neural development, neuronal differentiation, neurite outgrowth, and specification. These factors are involved in the regulation of neurotransmission pathways and the modulation of several forms of synaptic plasticity. Due to NRGs’ role in synaptic plasticity, defects in their normal functioning are translated into altered signaling networks, which have been linked to susceptibility to developing psychiatric disorders like schizophrenia (SZ), autism, depression, and bipolar disorders. Additionally, deviation of the NRG normal functioning is involved in neurological diseases like Alzheimer’s and Parkinson’s disease. Contrastingly, NRG/ErbB signaling is also involved in the recovery after traumatic brain injuries (e.g., ischemic stroke). The NRG/ErbB signaling complex is highly unusual because the ligands (mainly NRG1–NRG3, with their multiple isoforms) and receptors (ErbB2–ErbB4) can orchestrate vast signaling complexes, with a wide reach within the processes that govern the development and appropriate function of the nervous system. This may explain why NRGs and ErbB receptor genes have been linked to complex brain disorders, like SZ. This review, are discussed important aspects of NRG and their relevance for nervous system functioning, including 1) subcellular localization, 2) signaling pathways involved in neuronal functions, 3) effect on neurite development and synapse formation, 4) modulation of some mechanisms of synaptic plasticity [long-term potentiation (LTP), depotentiation, long-term depression (LTD)] and 5) roles of NRGs in some neurological diseases. This review intends to present a summary of the main findings about this family of proteins, which might position them as one of the master regulators of brain functioning.
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神经调节蛋白:亚细胞定位、信号通路及其与神经可塑性和神经系统疾病的关系
神经调节蛋白(NRGs)及其同源ErbB受体(ErbB2-ErbB4)由6个不同的基因(NRG1-6)和许多亚型编码,在神经系统的发育和功能中起关键作用。已知NRGs调节神经系统的重要过程,如神经发育、神经元分化、神经突生长和规范。这些因素参与神经传递途径的调节和几种形式的突触可塑性的调节。由于NRGs在突触可塑性中的作用,其正常功能的缺陷被转化为信号网络的改变,这与精神分裂症(SZ)、自闭症、抑郁症和双相情感障碍等精神疾病的易感性有关。此外,NRG正常功能的偏离与阿尔茨海默病和帕金森病等神经系统疾病有关。相反,NRG/ErbB信号也参与创伤性脑损伤(如缺血性中风)后的恢复。NRG/ErbB信号复合物是非常不寻常的,因为配体(主要是NRG1-NRG3,及其多种异构体)和受体(ErbB2-ErbB4)可以协调大量的信号复合物,在控制神经系统发育和适当功能的过程中具有广泛的影响。这也许可以解释为什么NRGs和ErbB受体基因与复杂的脑部疾病有关,比如SZ。本文综述了NRG在神经系统功能中的重要作用,包括:1)亚细胞定位;2)参与神经元功能的信号通路;3)对神经突发育和突触形成的影响;4)突触可塑性的一些机制[长期增强(LTP),去增强(depotentiation),长期抑制(LTD)]的调节;5)NRG在一些神经系统疾病中的作用。本文综述了该蛋白家族的主要发现,这些发现可能将其定位为脑功能的主要调节因子之一。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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