p-21活化激酶(PAK)的药物抑制可恢复唐氏综合征细胞模型中受损的神经突生长和重塑。

IF 2.9 3区 医学 Q2 NEUROSCIENCES
Natalia Barraza-Núñez, Ramón Pérez-Núñez, Belén Gaete-Ramírez, Alejandra Barrios-Garrido, Christian Arriagada, Karen Poksay, Varghese John, Jean-Vianney Barnier, Ana María Cárdenas, Pablo Caviedes
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引用次数: 0

摘要

唐氏综合征(DS)的特征是21号染色体三体和认知缺陷,这与人类和动物模型中的神经元形态改变有关。编码淀粉样蛋白前体蛋白(APP)的基因存在于常染色体21中,其在退行性痴呆中的过度表达与神经元功能障碍、认知缺陷和阿尔茨海默病样痴呆有关。特别是,神经元扩展过程和分支的能力受到影响。目前的证据表明,APP还可以通过其在肌动蛋白细胞骨架中的作用,部分通过影响p21活化激酶(PAK)活性来调节神经突的生长。后一种效应是通过增加caspase切割释放的羧基末端C31片段的丰度来实现的。在这项工作中,我们使用来自人类DS动物模型16三体小鼠大脑皮层的CTb神经元细胞系,观察到APP过表达,caspase活性升高,APP c端片段的裂解增强,PAK1磷酸化增加。形态学分析表明,FRAX486抑制PAK1活性增加了神经突的平均长度、每个Sholl环的交叉数、新突起的形成和刺激突起的丧失。考虑到我们的结果,我们提出PAK过度磷酸化会损害DS细胞模型中的神经突生长和重塑,因此我们认为PAK1可能是一个潜在的药理学靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Pharmacological Inhibition of p-21 Activated Kinase (PAK) Restores Impaired Neurite Outgrowth and Remodeling in a Cellular Model of Down Syndrome.

Pharmacological Inhibition of p-21 Activated Kinase (PAK) Restores Impaired Neurite Outgrowth and Remodeling in a Cellular Model of Down Syndrome.

Down syndrome (DS) is characterized by the trisomy of chromosome 21 and by cognitive deficits that have been related to neuronal morphological alterations in humans, as well as in animal models. The gene encoding for amyloid precursor protein (APP) is present in autosome 21, and its overexpression in DS has been linked to neuronal dysfunction, cognitive deficit, and Alzheimer's disease-like dementia. In particular, the neuronal ability to extend processes and branching is affected. Current evidence suggests that APP could also regulate neurite growth through its role in the actin cytoskeleton, in part by influencing p21-activated kinase (PAK) activity. The latter effect is carried out by an increased abundance of the caspase cleavage-released carboxy-terminal C31 fragment. In this work, using a neuronal cell line named CTb, which derived from the cerebral cortex of a trisomy 16 mouse, an animal model of human DS, we observed an overexpression of APP, elevated caspase activity, augmented cleavage of the C-terminal fragment of APP, and increased PAK1 phosphorylation. Morphometric analyses showed that inhibition of PAK1 activity with FRAX486 increased the average length of the neurites, the number of crossings per Sholl ring, the formation of new processes, and stimulated the loss of processes. Considering our results, we propose that PAK hyperphosphorylation impairs neurite outgrowth and remodeling in the cellular model of DS, and therefore we suggest that PAK1 may be a potential pharmacological target.

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来源期刊
Neurotoxicity Research
Neurotoxicity Research 医学-神经科学
CiteScore
7.70
自引率
5.40%
发文量
164
审稿时长
6-12 weeks
期刊介绍: Neurotoxicity Research is an international, interdisciplinary broad-based journal for reporting both basic and clinical research on classical neurotoxicity effects and mechanisms associated with neurodegeneration, necrosis, neuronal apoptosis, nerve regeneration, neurotrophin mechanisms, and topics related to these themes. Published papers have focused on: NEURODEGENERATION and INJURY Neuropathologies Neuronal apoptosis Neuronal necrosis Neural death processes (anatomical, histochemical, neurochemical) Neurodegenerative Disorders Neural Effects of Substances of Abuse NERVE REGENERATION and RESPONSES TO INJURY Neural Adaptations Neurotrophin mechanisms and actions NEURO(CYTO)TOXICITY PROCESSES and NEUROPROTECTION Excitatory amino acids Neurotoxins, endogenous and synthetic Reactive oxygen (nitrogen) species Neuroprotection by endogenous and exogenous agents Papers on related themes are welcome.
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