D.Sc., University of Leipzig, Paul Flechsig Institute for Brain Research Jahnallee 59, 04109 Leipzig, Germany.
Am J Pathol. 2010 Jul;177(1):15-20. doi: 10.2353/ajpath.2010.090955. Epub 2010 May 14.
Aneuploidy, an abnormal number of copies of a genomic region, might be a significant source for neuronal complexity, intercellular diversity, and evolution. Genomic instability associated with aneuploidy, however, can also lead to developmental abnormalities and decreased cellular fitness. Here we show that neurons with a more-than-diploid content of DNA are increased in preclinical stages of Alzheimer's disease (AD) and are selectively affected by cell death during progression of the disease. Present findings show that neuronal hyperploidy in AD is associated with a decreased viability. Hyperploidy of neurons thus represents a direct molecular signature of cells prone to death in AD and indicates that a failure of neuronal differentiation is a critical pathogenetic event in AD.
非整倍体,即基因组区域的拷贝数异常,可能是神经元复杂性、细胞间多样性和进化的重要来源。然而,与非整倍体相关的基因组不稳定性也可能导致发育异常和细胞活力下降。在这里,我们发现在阿尔茨海默病(AD)的临床前阶段,DNA 含量超过二倍体的神经元数量增加,并且在疾病进展过程中,这些神经元会选择性地受到细胞死亡的影响。目前的研究结果表明,AD 中神经元的多倍体与存活能力下降有关。因此,神经元的多倍体代表了 AD 中易于死亡的细胞的直接分子特征,并表明神经元分化失败是 AD 的一个关键发病事件。