Department of Biomedicine, University of Aarhus, Aarhus, Denmark.
Brain Pathol. 2012 Jan;22(1):99-109. doi: 10.1111/j.1750-3639.2011.00545.x.
Dementias are a varied group of disorders typically associated with memory loss, impaired judgment and/or language and by symptoms affecting other cognitive and social abilities to a degree that interferes with daily functioning. Alzheimer's disease (AD) is the most common cause of a progressive dementia, followed by dementia with Lewy bodies (DLB), frontotemporal dementia (FTD), (VaD) and HIV-associated neurocognitive disorders (HAND). The pathogenesis of this group of disorders has been linked to the abnormal accumulation of proteins in the brains of affected individuals, which in turn has been related to deficits in protein clearance. Autophagy is a key cellular protein clearance pathway with proteolytic cleavage and degradation via the ubiquitin-proteasome pathway representing another important clearance mechanism. Alterations in the levels of autophagy and the proteins associated with the autophagocytic pathway have been reported in various types of dementias. This review will examine recent literature across these disorders and highlight a common theme of altered autophagy across the spectrum of the dementias.
痴呆症是一组多种障碍的统称,通常与记忆力减退、判断力受损和/或语言障碍有关,并伴有其他认知和社交能力的症状,这些症状会严重影响日常生活功能。阿尔茨海默病(AD)是最常见的进行性痴呆症的原因,其次是路易体痴呆症(DLB)、额颞叶痴呆症(FTD)、血管性痴呆症(VaD)和 HIV 相关的神经认知障碍(HAND)。该类疾病的发病机制与受影响个体大脑中蛋白质的异常积累有关,而这又与蛋白质清除缺陷有关。自噬是一种关键的细胞蛋白清除途径,通过泛素-蛋白酶体途径进行蛋白水解和降解,是另一种重要的清除机制。在各种类型的痴呆症中,已经报道了自噬水平和与自噬途径相关的蛋白质的改变。本综述将检查这些疾病的最新文献,并强调在痴呆症谱中自噬改变的共同主题。