Age-dependent changes in the subcallosal zone neurogenesis of mice

被引:6
|
作者
Kim, Hyun Jung [1 ]
Kim, Joo Yeon [1 ]
Sun, Woong [1 ]
机构
[1] Korea Univ, Coll Med, Dept Anat, Seoul 136705, South Korea
基金
新加坡国家研究基金会;
关键词
Aging; Neural stem cell; Neurogenesis; Traumatic brain injury; Subcallosal zone; NEURAL STEM-CELLS; CENTRAL-NERVOUS-SYSTEM; ADULT MAMMALIAN BRAIN; SUBVENTRICULAR ZONE; DENTATE GYRUS; NEURONS; PROLIFERATION; HIPPOCAMPUS; DIFFERENTIATION; ORGANIZATION;
D O I
10.1016/j.neuint.2012.02.027
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
There are several known neurogenic areas including subventricular zone and subgranular layer in the dentate gyrus of the hippocampus. Both germinal centers exhibit an age-dependent decline in cell proliferation and neurogenesis, which may be associated with age-related decline in brain function. We recently identified the subcallosal zone (SCZ) as a novel neural stem cell niche with a potential to spontaneously produce new neuroblasts. We examined whether SCZ neurogenesis is also regulated by the age of mice. The number of newly generated neuroblasts was reduced in the SCZ with age, and only marginal number of DCX-labeled neuroblasts was found in 6-month-old SCZ, which is most likely due to reduced proliferation of progenitor cells and loss of neural stem cells (NSCs). This age-dependent changes in the SCZ occurred earlier than that of other neurogenic brain regions. The neurosphere assay in vitro confirmed the depletion of NSCs within the SCZ of young adults. However, marked induction of neuroblast production in the SCZ was seen in 6-month-old mice after traumatic brain injury. Taken together, these results indicate that a rapid decline in SCZ neurogenesis in mice is due to depletion of NSCs and reduced capacity to produce neuroblasts. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:879 / 884
页数:6
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