Zaidi Asma, Adewale Mercy, McLean Lauren, Ramlow Paul
Division of Basic Sciences, Kansas City University of Medicine and Biosciences, 1750 Independence Avenue, Kansas City, MO 64106, USA.
Division of Basic Sciences, Kansas City University of Medicine and Biosciences, 1750 Independence Avenue, Kansas City, MO 64106, USA.
Neurosci Lett. 2018 Jan 10;663:12-17. doi: 10.1016/j.neulet.2017.09.066.
The plasma membrane Ca-ATPase (PMCA) pumps play a critical role in the maintenance of calcium (Ca) homeostasis, crucial for optimal neuronal function and cell survival. Loss of Ca homeostasis is a key precursor in neuronal dysfunction associated with brain aging and in the pathogenesis of neurodegenerative disorders. In this article, we review evidence showing age-related changes in the PMCAs in synaptic plasma membranes (SPMs) and lipid raft microdomains isolated from rat brain. Both PMCA activity and protein levels decline progressively with increasing age. However, the loss of activity is disproportionate to the reduction of protein levels suggesting the presence of dysfunctional PMCA molecules in aged brain. PMCA activity is also diminished in post-mortem human brain samples from Alzheimer's disease and Parkinson's disease patients and in cell models of these neurodegenerative disorders. Experimental reduction of the PMCAs not only alter Ca homeostasis but also have diverse effects on neurons such as reduced neuritic network, impaired release of neurotransmitter and increased susceptibility to stressful stimuli, particularly to agents that elevate intracellular Ca [Ca]. Loss of PMCA is likely to contribute to neuronal dysfunction observed in the aging brain and in the development of age-dependent neurodegenerative disorders. Therapeutic (pharmacological and/or non-pharmacological) approaches that can enhance PMCA activity and stabilize [Ca] homeostasis may be capable of preventing, slowing, and/or reversing neuronal degeneration.
质膜钙 - ATP酶(PMCA)泵在维持钙(Ca)稳态中起着关键作用,而钙稳态对于最佳神经元功能和细胞存活至关重要。钙稳态的丧失是与脑老化相关的神经元功能障碍以及神经退行性疾病发病机制的关键先兆。在本文中,我们综述了有关从大鼠脑中分离出的突触质膜(SPM)和脂筏微结构域中PMCA随年龄变化的证据。随着年龄的增长,PMCA活性和蛋白质水平均逐渐下降。然而,活性的丧失与蛋白质水平的降低不成比例,这表明老年脑中存在功能失调的PMCA分子。在阿尔茨海默病和帕金森病患者的死后人类脑样本以及这些神经退行性疾病的细胞模型中,PMCA活性也有所降低。实验性降低PMCA不仅会改变钙稳态,还会对神经元产生多种影响,如神经突网络减少、神经递质释放受损以及对应激刺激(特别是升高细胞内Ca [Ca]的物质)的易感性增加。PMCA的丧失可能导致在老化大脑中观察到的神经元功能障碍以及年龄依赖性神经退行性疾病的发展。能够增强PMCA活性并稳定[Ca]稳态的治疗方法(药物和/或非药物)可能能够预防、减缓和/或逆转神经元变性。