Yao P J, Coleman P D
Department of Neurobiology and Anatomy, University of Rochester Medical Center, NY 14642, USA.
Neurosci Lett. 1998 Aug 7;252(1):33-6. doi: 10.1016/s0304-3940(98)00547-3.
Synapse loss is one of the neuropathologies in Alzheimer's disease (AD) that may play a crucial role in the mechanism of its distinct cognitive impairment and dementia. In a previous study [18], a significant reduction of O-glycosylated clathrin assembly protein AP180 was observed in neocortex of AD. The reduction correlated with the density of neurofibrillary tangles. In this study we further determine that the O-GlcNAc/AP180 ratio is not changed, but the level of AP180 protein decreases in AD. Furthermore, whereas the level of neurofilament (NF-M) remains relatively unchanged, another clathrin assembly protein, AP-2, is also reduced in AD along with a small loss of synaptophysin. Our findings suggest that synaptic vesicle recycling dysfunction may be involved in the pathology of synapse loss in AD.
突触丢失是阿尔茨海默病(AD)的神经病理学特征之一,可能在其独特的认知障碍和痴呆机制中起关键作用。在先前的一项研究[18]中,观察到AD患者新皮质中O-糖基化网格蛋白组装蛋白AP180显著减少。这种减少与神经原纤维缠结的密度相关。在本研究中,我们进一步确定AD患者中O-GlcNAc/AP180比值未改变,但AP180蛋白水平降低。此外,虽然神经丝(NF-M)水平相对保持不变,但另一种网格蛋白组装蛋白AP-2在AD中也减少,同时突触素略有丢失。我们的研究结果表明,突触小泡循环功能障碍可能参与了AD突触丢失的病理过程。