4.7 Article

Evidences for Adult Hippocampal Neurogenesis in Humans

期刊

JOURNAL OF NEUROSCIENCE
卷 41, 期 12, 页码 2541-2553

出版社

SOC NEUROSCIENCE
DOI: 10.1523/JNEUROSCI.0675-20.2020

关键词

adult neurogenesis; controversy; human; methodology; hippocampus; immature neuron

资金

  1. Spanish Ministry of Economy and Competitiveness [SAF-2017-82185-R, RYC-2015-171899]
  2. Alzheimer's Association [2015-NIRG-340709, AARG-17-528125]
  3. Association for Frontotemporal Degeneration 2016 Basic Science Pilot Grant
  4. Comunidad de Madrid [PEJD-2017-PRE/BMD-3439]
  5. Fundacion Ramon Areces and Banco de Santander
  6. Beca Predoctoral en Neurociencias Fundacion Tatiana Perez de Guzman fellowship
  7. Universidad Autonoma de Madrid Doctorate fellowship FPIUAM 2017 program
  8. Formacion de personal Investigador contract
  9. Spanish Ministry for Economy and Competitiveness [PRE2018-085233]

向作者/读者索取更多资源

The rodent hippocampus generates new neurons throughout life, but direct evidence of adult neurogenesis in humans remains elusive. Research indicates that adult hippocampal neurogenesis may persist until the 10th decade of human life, with marked impairments in patients with Alzheimer's disease. Methodological aspects in processing and analyzing postmortem human brain samples may limit the detection of markers of adult hippocampal neurogenesis, highlighting the need for strict controls in human studies.
The rodent hippocampus generates new neurons throughout life. This process, named adult hippocampal neurogenesis (AHN), is a striking form of neural plasticity that occurs in the brains of numerous mammalian species. Direct evidence of adult neurogenesis in humans has remained elusive, although the occurrence of this phenomenon in the human dentate gyrus has been demonstrated in seminal studies and recent research that have applied distinct approaches to birthdate newly generated neurons and to validate markers of adult-born neurons. Our data point to the persistence of AHN until the 10th decade of human life, as well as to marked impairments in this process in patients with Alzheimer's disease. Moreover, our work demonstrates that the methods used to process and analyze postmortem human brain samples can limit the detection of various markers of AHN to the point of making them undetectable. In this Dual Perspectives article, we highlight the critical methodological aspects that should be strictly controlled in human studies and the robust evidence that supports the occurrence of AHN in humans. We also put forward reasons that may account for current discrepancies on this topic. Finally, the unresolved questions and future challenges awaiting the field are highlighted.

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