Du Heng, Guo Lan, Wu Xiaoping, Sosunov Alexander A, McKhann Guy M, Chen John Xi, Yan Shirley ShiDu
Department of Pharmacology and Toxicology, and Higuchi Bioscience Center, School of Pharmacy, University of Kansas, Lawrence, KS 66047, USA.
Department of Neurosurgery, Physicians & Surgeons College of Columbia University, New York, NY 10032, USA.
Biochim Biophys Acta. 2014 Dec;1842(12 Pt A):2517-27. doi: 10.1016/j.bbadis.2013.03.004. Epub 2013 Mar 16.
The coexistence of neuronal mitochondrial pathology and synaptic dysfunction is an early pathological feature of Alzheimer's disease (AD). Cyclophilin D (CypD), an integral part of mitochondrial permeability transition pore (mPTP), is involved in amyloid beta (Aβ)-instigated mitochondrial dysfunction. Blockade of CypD prevents Aβ-induced mitochondrial malfunction and the consequent cognitive impairments. Here, we showed the elimination of reactive oxygen species (ROS) by antioxidants probucol or superoxide dismutase (SOD)/catalase blocks Aβ-mediated inactivation of protein kinase A (PKA)/cAMP regulatory-element-binding (CREB) signal transduction pathway and loss of synapse, suggesting the detrimental effects of oxidative stress on neuronal PKA/CREB activity. Notably, neurons lacking CypD significantly attenuate Aβ-induced ROS. Consequently, CypD-deficient neurons are resistant to Aβ-disrupted PKA/CREB signaling by increased PKA activity, phosphorylation of PKA catalytic subunit (PKA C), and CREB. In parallel, lack of CypD protects neurons from Aβ-induced loss of synapses and synaptic dysfunction. Furthermore, compared to the mAPP mice, CypD-deficient mAPP mice reveal less inactivation of PKA-CREB activity and increased synaptic density, attenuate abnormalities in dendritic spine maturation, and improve spontaneous synaptic activity. These findings provide new insights into a mechanism in the crosstalk between the CypD-dependent mitochondrial oxidative stress and signaling cascade, leading to synaptic injury, functioning through the PKA/CREB signal transduction pathway.
神经元线粒体病理与突触功能障碍并存是阿尔茨海默病(AD)的早期病理特征。亲环素D(CypD)是线粒体通透性转换孔(mPTP)的一个组成部分,参与淀粉样β蛋白(Aβ)引发的线粒体功能障碍。阻断CypD可预防Aβ诱导的线粒体功能障碍及随之而来的认知障碍。在此,我们发现抗氧化剂普罗布考或超氧化物歧化酶(SOD)/过氧化氢酶清除活性氧(ROS)可阻断Aβ介导的蛋白激酶A(PKA)/环磷酸腺苷反应元件结合蛋白(CREB)信号转导通路失活及突触丧失,提示氧化应激对神经元PKA/CREB活性具有有害影响。值得注意的是,缺乏CypD的神经元可显著减轻Aβ诱导的ROS。因此,缺乏CypD的神经元通过增加PKA活性、PKA催化亚基(PKA C)磷酸化和CREB,对Aβ破坏的PKA/CREB信号具有抗性。同时,缺乏CypD可保护神经元免受Aβ诱导的突触丧失和突触功能障碍。此外,与mAPP小鼠相比,缺乏CypD的mAPP小鼠显示出PKA-CREB活性失活减少、突触密度增加、树突棘成熟异常减轻及自发突触活动改善。这些发现为CypD依赖性线粒体氧化应激与信号级联之间的串扰机制提供了新见解,该机制通过PKA/CREB信号转导通路导致突触损伤。