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冬眠仓鼠新皮质和海马神经元高尔基体的变化

Changes in the Golgi Apparatus of Neocortical and Hippocampal Neurons in the Hibernating Hamster.

作者信息

Antón-Fernández Alejandro, León-Espinosa Gonzalo, DeFelipe Javier, Muñoz Alberto

机构信息

Departamento de Neurobiología Funcional y de Sistemas, Instituto Cajal, CSIC Madrid, Spain ; Laboratorio Cajal de Circuitos Corticales, Centro de Tecnología Biomédica, Universidad Politécnica de Madrid Madrid, Spain.

Departamento de Neurobiología Funcional y de Sistemas, Instituto Cajal, CSIC Madrid, Spain ; Laboratorio Cajal de Circuitos Corticales, Centro de Tecnología Biomédica, Universidad Politécnica de Madrid Madrid, Spain ; Facultad de Farmacia, Universidad San Pablo CEU Madrid, Spain.

出版信息

Front Neuroanat. 2015 Dec 15;9:157. doi: 10.3389/fnana.2015.00157. eCollection 2015.

Abstract

Hibernating animals have been used as models to study several aspects of the plastic changes that occur in the metabolism and physiology of neurons. These models are also of interest in the study of Alzheimer's disease because the microtubule-associated protein tau is hyperphosphorylated during the hibernation state known as torpor, similar to the pretangle stage of Alzheimer's disease. Hibernating animals undergo torpor periods with drops in body temperature and metabolic rate, and a virtual cessation of neural activity. These processes are accompanied by morphological and neurochemical changes in neurons, which reverse a few hours after coming out of the torpor state. Since tau has been implicated in the structural regulation of the neuronal Golgi apparatus (GA) we have used Western Blot and immunocytochemistry to analyze whether the GA is modified in cortical neurons of the Syrian hamster at different hibernation stages. The results show that, during the hibernation cycle, the GA undergo important structural changes along with differential modifications in expression levels and distribution patterns of Golgi structural proteins. These changes were accompanied by significant transitory reductions in the volume and surface area of the GA elements during torpor and arousal stages as compared with euthermic animals.

摘要

冬眠动物已被用作模型,以研究神经元代谢和生理过程中发生的可塑性变化的多个方面。这些模型在阿尔茨海默病的研究中也备受关注,因为在被称为“蛰伏”的冬眠状态下,微管相关蛋白tau会发生过度磷酸化,这与阿尔茨海默病的缠结前期相似。冬眠动物会经历体温和代谢率下降以及神经活动几乎停止的蛰伏期。这些过程伴随着神经元的形态和神经化学变化,这些变化在从蛰伏状态苏醒后几小时内会逆转。由于tau与神经元高尔基体(GA)的结构调节有关,我们使用蛋白质免疫印迹法和免疫细胞化学方法来分析叙利亚仓鼠皮质神经元在不同冬眠阶段高尔基体是否发生改变。结果表明,在冬眠周期中,高尔基体经历了重要的结构变化,同时高尔基体结构蛋白的表达水平和分布模式也发生了不同的改变。与正常体温的动物相比,在蛰伏期和苏醒期,这些变化伴随着高尔基体元件的体积和表面积显著短暂减少。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c78d/4678224/52cbfec8d00d/fnana-09-00157-g0001.jpg

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