Department of Medicine, UCSF Medical Center and the Jewish Home of San Francisco San Francisco, California.
Memory and Aging Center, Department of Neurology, UCSF Medical Center San Francisco, California.
Ann Clin Transl Neurol. 2015 Jul;2(7):769-73. doi: 10.1002/acn3.211. Epub 2015 May 13.
Transcription factors that mediate neuronal defenses against diverse stresses were quantified in plasma neural-derived exosomes of Alzheimer's disease or frontotemporal dementia patients and matched controls. Exosomal levels of low-density lipoprotein receptor-related protein 6, heat-shock factor-1, and repressor element 1-silencing transcription factor all were significantly lower in Alzheimer's disease patients than controls (P < 0.0001). In frontotemporal dementia, the only significant difference was higher levels of repressor element 1-silencing transcription factor than in controls. Exosomal transcription factors were diminished 2-10 years before clinical diagnosis of Alzheimer's disease. Low exosomal levels of survival proteins may explain decreased neuronal resistance to Alzheimer's disease neurotoxic proteins.
在阿尔茨海默病或额颞叶痴呆患者和匹配对照者的血浆神经源性外泌体中,定量了介导神经元防御多种应激的转录因子。阿尔茨海默病患者的外泌体中载脂蛋白受体相关蛋白 6、热休克因子 1 和阻遏元件 1 沉默转录因子的水平均显著低于对照组(P < 0.0001)。在额颞叶痴呆中,唯一显著的差异是阻遏元件 1 沉默转录因子的水平高于对照组。外泌体转录因子在阿尔茨海默病临床诊断前 2-10 年就已经减少。存活蛋白的低外泌体水平可能解释了神经元对阿尔茨海默病神经毒性蛋白的抵抗能力下降。