Tokyo Metropolitan Institute of Medical Science, Setagaya-ku, Tokyo, Japan.
PCND Neuroscience Research Institute, Poway, CA, USA.
J Alzheimers Dis. 2019;68(2):473-481. doi: 10.3233/JAD-180986.
Alzheimer's disease (AD), the most common neurodegenerative dementia, leads to memory dysfunction due to widespread neuronal loss associated with aggregation of amyloidogenic proteins (APs), while schizophrenia (SCZ) represents a major psychiatric disorder characterized by delusions, hallucinations, and other cognitive abnormalities, the underlying mechanisms of which remain obscure. Although AD and SCZ partially overlap in terms of psychiatric symptoms and some aspects of cognitive impairment, the causal relationship between AD and SCZ is unclear. Based on the similarity of APs with yeast prion in terms of stress-induced protein aggregation, we recently proposed that evolvability of APs might be an epigenetic phenomenon to transmit stress information of parental brain to cope with the stressors in offspring. Although amyloid evolvability may be beneficial in evolution, AD might be manifested during parental aging as the mechanism of antagonistic pleiotropy phenomenon. Provided that accumulating evidence implicates stress as an important factor in SCZ, the main objective of this paper is to better understand the possible connection of AD and SCZ through amyloid evolvability. Hypothetically, the delivery of information of stress by APs may be less efficient under the decreased evolvability conditions such as disease-modifying treatment, leading to SCZ in offspring. Conversely, the increased evolvability conditions including gene mutations of APs are supposed to be beneficial for offspring, but might lead to AD in parents. Collectively, AD and SCZ might transgenerationally interfere with each other through amyloid evolvability, and this could explain why both AD and SCZ have not been selected out through evolution.
阿尔茨海默病(AD)是最常见的神经退行性痴呆症,由于与淀粉样蛋白(AP)聚集相关的广泛神经元丢失,导致记忆功能障碍,而精神分裂症(SCZ)则代表一种主要的精神障碍,其特征为妄想、幻觉和其他认知异常,但其潜在机制仍不清楚。虽然 AD 和 SCZ 在精神症状和某些认知障碍方面部分重叠,但 AD 和 SCZ 之间的因果关系尚不清楚。基于 AP 与酵母朊病毒在应激诱导蛋白聚集方面的相似性,我们最近提出,AP 的可进化性可能是一种表观遗传现象,可将亲代大脑的应激信息传递给后代,以应对后代的应激源。虽然淀粉样蛋白的可进化性在进化中可能是有益的,但 AD 可能在亲代衰老时表现出来,这是拮抗多效性现象的机制。鉴于越来越多的证据表明应激是 SCZ 的一个重要因素,本文的主要目的是通过淀粉样蛋白的可进化性更好地理解 AD 和 SCZ 之间的可能联系。假设在疾病修饰治疗等可进化性降低的情况下,AP 通过传递应激信息的效率可能会降低,从而导致后代出现 SCZ。相反,包括 AP 基因突变在内的可进化性增加的条件对后代是有益的,但可能导致亲代出现 AD。总的来说,AD 和 SCZ 可能通过淀粉样蛋白的可进化性相互干扰,这可以解释为什么 AD 和 SCZ 在进化过程中都没有被淘汰。