Lopez-Ortega Elena, Ruiz Rocío, Tabares Lucia
Department of Medical Physiology and Biophysics, School of Medicine, University of Seville Seville, Spain.
Department of Biochemistry and Molecular Biology, School of Pharmacy, University of Seville Seville, Spain.
Front Neurosci. 2017 Feb 10;11:39. doi: 10.3389/fnins.2017.00039. eCollection 2017.
Cysteine string protein α (CSPα) is a vesicle protein located in the presynaptic terminal of most synapses. CSPα is an essential molecular co-chaperone that facilitates the correct folding of proteins and the assembly of the exocytic machinery. The absence of this protein leads to altered neurotransmitter release and neurodegeneration in multiple model systems, from flies to mice. In humans, CSPα mutations are associated with the development of neuronal ceroid lipofuscinosis (NCL), a neurodegenerative disease characterized by intracellular accumulation of lysosomal material. Here, we review the physiological role of CSPα and the pathology resulting from the homozygous deletion of the gene or its mutations. In addition, we investigate whether long-term moderate reduction of the protein produces motor dysfunction. We found that 1-year-old CSPα heterozygous mice display a reduced ability to sustain motor unit recruitment during repetitive stimulation, which indicates that physiological levels of CSPα are required for normal neuromuscular responses in mice and, likely, in humans.
半胱氨酸串珠蛋白α(CSPα)是一种位于大多数突触前突触末端的囊泡蛋白。CSPα是一种重要的分子共伴侣蛋白,可促进蛋白质的正确折叠和胞吐机制的组装。在从果蝇到小鼠的多个模型系统中,这种蛋白质的缺失会导致神经递质释放改变和神经退行性变。在人类中,CSPα突变与神经元蜡样脂褐质沉积症(NCL)的发生有关,NCL是一种神经退行性疾病,其特征是溶酶体物质在细胞内积聚。在这里,我们综述了CSPα的生理作用以及该基因纯合缺失或其突变所导致的病理学。此外,我们研究了该蛋白的长期适度减少是否会产生运动功能障碍。我们发现,1岁的CSPα杂合小鼠在重复刺激期间维持运动单位募集的能力降低,这表明CSPα的生理水平对于小鼠以及可能对于人类的正常神经肌肉反应是必需的。