Department of Molecular Neuropathology, Centro de Biología Molecular "Severo Ochoa" (CBMSO), Spanish Research Council (CSIC), Universidad Autónoma de Madrid (UAM), Madrid, Spain.
Department of Molecular Biology, Faculty of Sciences, Universidad Autónoma de Madrid, Madrid, Spain.
Science. 2021 Nov 26;374(6571):1106-1113. doi: 10.1126/science.abl5163. Epub 2021 Oct 21.
Disrupted hippocampal performance underlies psychiatric comorbidities and cognitive impairments in patients with neurodegenerative disorders. To understand the contribution of adult hippocampal neurogenesis (AHN) to amyotrophic lateral sclerosis, Huntington’s disease, Parkinson’s disease, dementia with Lewy bodies, and frontotemporal dementia, we studied postmortem human samples. We found that adult-born dentate granule cells showed abnormal morphological development and changes in the expression of differentiation markers. The ratio of quiescent to proliferating hippocampal neural stem cells shifted, and the homeostasis of the neurogenic niche was altered. Aging and neurodegenerative diseases reduced the phagocytic capacity of microglia, triggered astrogliosis, and altered the microvasculature of the dentate gyrus. Thus, enhanced vulnerability of AHN to neurodegeneration might underlie hippocampal dysfunction during physiological and pathological aging in humans.
海马功能障碍是神经退行性疾病患者伴发精神疾病和认知障碍的基础。为了了解成人海马神经发生(AHN)对肌萎缩侧索硬化症、亨廷顿病、帕金森病、路易体痴呆和额颞叶痴呆的贡献,我们研究了尸检的人类样本。我们发现,新生的齿状回颗粒细胞表现出异常的形态发育和分化标志物表达的变化。静息和增殖的海马神经干细胞的比例发生了改变,神经发生龛的内稳态被改变。衰老和神经退行性疾病降低了小胶质细胞的吞噬能力,引发了星形胶质细胞增生,并改变了齿状回的微血管。因此,AHN 对神经退行性变的易感性增加可能是人类生理和病理性衰老过程中海马功能障碍的基础。