Papuć Ewa, Rejdak Konrad
Department of Neurology, Medical University of Lublin, Lublin, Poland.
Medical Research Center, Polish Academy of Sciences, Warsaw, Poland.
Arch Med Sci. 2018 Aug 28;16(2):345-351. doi: 10.5114/aoms.2018.76863. eCollection 2020.
Although Alois Alzheimer described myelin disruption in Alzheimer's disease (AD) as early as in 1911, his observation has escaped the attention of researchers since that time. Alzheimer's disease has been mainly considered as a grey matter disorder; nevertheless, recent evidence suggests that myelin impairment may play an important role in AD pathology. Classical neuropathological changes in AD, e.g. the accumulation of aggregated Aβ 42 and the presence of neurofibrillary tangles, are responsible for neuronal loss, but they may also induce death of oligodendrocytes and myelin damage. There is also evidence that myelin pathology may even precede Aβ and tau pathologies in AD. The state of the art does not allow us to determine whether myelin damage is a primary or a secondary injury in AD subjects. The article presents an overview of current knowledge on the role of myelin in AD pathology and its interactions with Aβ and tau pathologies.
尽管阿洛伊斯·阿尔茨海默早在1911年就描述了阿尔茨海默病(AD)中的髓鞘破坏,但从那时起他的观察就一直未引起研究人员的注意。阿尔茨海默病一直主要被视为一种灰质疾病;然而,最近的证据表明髓鞘损伤可能在AD病理中起重要作用。AD中的经典神经病理学变化,例如聚集的Aβ 42的积累和神经原纤维缠结的存在,是神经元丢失的原因,但它们也可能导致少突胶质细胞死亡和髓鞘损伤。也有证据表明,在AD中髓鞘病理甚至可能先于Aβ和tau病理出现。目前的技术水平尚无法让我们确定在AD患者中髓鞘损伤是原发性损伤还是继发性损伤。本文概述了目前关于髓鞘在AD病理中的作用及其与Aβ和tau病理相互作用的知识。