Department of Pathology and Cell Biology, Groupe de Recherche sur le Système Nerveux Central, Centre of Excellence in Neuroscience of the Université de Montréal, Université de Montréal, Montréal, Canada.
Eur J Neurosci. 2013 Jun;37(12):1978-86. doi: 10.1111/ejn.12207.
In the brains of adult vertebrates, including humans, neurogenesis occurs in restricted niches where it maintains cellular turnover and cognitive plasticity. In virtually all species, however, aging is associated with a significant decline in adult neurogenesis. Moreover, an acceleration of neurogenic defects is observed in models of Alzheimer's disease and other neurodegenerative diseases, suggesting an involvement in aging- and disease-associated cognitive deficits. To gain insights into when, how and why adult neurogenesis decreases in the aging brain, we critically reviewed the scientific literature on aging of the rodent subventricular zone, the neurogenic niche of the adult forebrain. Our analysis revealed that deficits in the neurogenic pathway are largely established by middle age, but that there remains striking ambiguity in the underlying mechanisms, especially at the level of stem and progenitor cells. We identify and discuss several challenging issues that have contributed to these key gaps in our current knowledge. In the future, addressing these issues should help untangle the interactions between neurogenesis, aging and aging-associated diseases.
在包括人类在内的成年脊椎动物的大脑中,神经发生发生在限制其细胞更替和认知可塑性的特定部位。然而,在几乎所有物种中,衰老与成年神经发生的显著下降有关。此外,在阿尔茨海默病和其他神经退行性疾病的模型中观察到神经发生缺陷的加速,表明其与衰老和疾病相关的认知缺陷有关。为了深入了解成年神经发生在衰老大脑中何时、如何以及为何减少,我们批判性地回顾了关于啮齿动物侧脑室下区(成年前脑的神经发生部位)衰老的科学文献。我们的分析表明,神经发生途径的缺陷主要在中年就已确立,但潜在机制仍存在很大的不确定性,尤其是在干细胞和祖细胞水平。我们确定并讨论了几个具有挑战性的问题,这些问题导致了我们目前知识中的这些关键差距。在未来,解决这些问题应该有助于理清神经发生、衰老和与衰老相关疾病之间的相互作用。