Early-life stress restricts the capacity of adult progenitor cells to differentiate into neurons.
Early-life stress restricts the capacity of adult progenitor cells to differentiate into neurons.
复制标题
生命早期的压力限制了成年祖细胞分化为神经元的能力。
DOI:
10.1016/j.biopsych.2014.11.008
复制
发表时间:
2015
影响因子:
10.6
通讯作者:
Kaffman,Arie
中科院分区:
文献类型:
--
作者:
Kaffman,Arie
Exposure to childhood abuse or neglect is associated with abnormal hippocampal function in adulthood. The molecular mechanisms by which early adversity modifies hippocampal function in adulthood are currently poorly understood in humans. However, similar findings in rodents and nonhuman primates suggest that animal models may provide important insights into this issue (1). One of the main challenges of studying hippocampal tissue in animal models has been the cellular heterogeneity of the hippocampus, where different cell types (eg, stem cells, pyramidal cells, granule cells, interneurons, astrocytes, microglia, and oligodendrocytes) respond differently to stress, yet they are closely packed and interact with one another. The challenge has been to figure out how to harvest and study the effects of early-life stress in a homogeneous cell population in a manner that recapitulates the cellular response in the intact hippocampus. In this issue of Biological Psychiatry, Boku et al.(2) used an in vitro system to show that exposure to stress early in life restricts the capacity of adult progenitor cells to differentiate into neurons. This is an important first step in studying the effects of early adversity using a homogeneous cell population harvested from the hippocampus, and it demonstrates the advantages and the pitfalls of this reductionistic approach.