Huang Songqiang, Dong Wanting, Lin Xiaoqian, Bian Jinsong
Department of Pharmacology, Joint Laboratory of Guangdong-Hong Kong Universities for Vascular Homeostasis and Diseases, School of Medicine, Southern University of Science and Technology, Shenzhen, Guangdong Province, China.
Department of Pharmacology, School of Basic Medicine, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei Province, China.
Neural Regen Res. 2024 Dec 1;19(12):2684-2697. doi: 10.4103/NRR.NRR-D-23-01175. Epub 2024 Jan 31.
Na+/K+-ATPase is a transmembrane protein that has important roles in the maintenance of electrochemical gradients across cell membranes by transporting three Na+ out of and two K+ into cells. Additionally, Na+/K+-ATPase participates in Ca2+-signaling transduction and neurotransmitter release by coordinating the ion concentration gradient across the cell membrane. Na+/K+-ATPase works synergistically with multiple ion channels in the cell membrane to form a dynamic network of ion homeostatic regulation and affects cellular communication by regulating chemical signals and the ion balance among different types of cells. Therefore, it is not surprising that Na+/K+-ATPase dysfunction has emerged as a risk factor for a variety of neurological diseases. However, published studies have so far only elucidated the important roles of Na+/K+-ATPase dysfunction in disease development, and we are lacking detailed mechanisms to clarify how Na+/K+-ATPase affects cell function. Our recent studies revealed that membrane loss of Na+/K+-ATPase is a key mechanism in many neurological disorders, particularly stroke and Parkinson's disease. Stabilization of plasma membrane Na+/K+-ATPase with an antibody is a novel strategy to treat these diseases. For this reason, Na+/K+-ATPase acts not only as a simple ion pump but also as a sensor/regulator or cytoprotective protein, participating in signal transduction such as neuronal autophagy and apoptosis, and glial cell migration. Thus, the present review attempts to summarize the novel biological functions of Na+/K+-ATPase and Na+/K+-ATPase-related pathogenesis. The potential for novel strategies to treat Na+/K+-ATPase-related brain diseases will also be discussed.
钠钾ATP酶是一种跨膜蛋白,通过将三个钠离子转运出细胞并将两个钾离子转运入细胞,在维持细胞膜两侧的电化学梯度方面发挥着重要作用。此外,钠钾ATP酶通过协调细胞膜两侧的离子浓度梯度参与钙信号转导和神经递质释放。钠钾ATP酶与细胞膜中的多个离子通道协同工作,形成一个动态的离子稳态调节网络,并通过调节化学信号和不同类型细胞之间的离子平衡来影响细胞间通讯。因此,钠钾ATP酶功能障碍已成为多种神经疾病的危险因素也就不足为奇了。然而,迄今为止已发表的研究仅阐明了钠钾ATP酶功能障碍在疾病发展中的重要作用,我们仍缺乏详细的机制来阐明钠钾ATP酶如何影响细胞功能。我们最近的研究表明,钠钾ATP酶的膜丢失是许多神经疾病的关键机制,尤其是中风和帕金森病。用抗体稳定质膜钠钾ATP酶是治疗这些疾病的一种新策略。因此,钠钾ATP酶不仅作为一种简单的离子泵,还作为一种传感器/调节器或细胞保护蛋白,参与神经元自噬和凋亡以及胶质细胞迁移等信号转导。因此,本综述试图总结钠钾ATP酶的新生物学功能以及与钠钾ATP酶相关的发病机制。还将讨论治疗与钠钾ATP酶相关的脑部疾病的新策略的潜力。