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Neural Stem Cells Show Bidirectional Experience-Dependent Plasticity in the Perinatal Mammalian Brain

机译:神经干细胞在围产期哺乳动物脑中显示双向经验依赖可塑性。

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摘要

Many of the effects of prenatal stress on the endocrine function, brain morphology, and behavior in mammals can be reversed by brief sessions of postnatal separation and handling. We have tested the hypothesis that the effects of both the prenatal and postnatal experiences are mediated by negative and positive regulation of neural stem cell (NSC) number during critical stages in neurodevelopment. We used thein vitroclonal neurosphere assay to quantify NSCs in hamsters that had experienced prenatal stress (maternal restraint stress for 2 hr per day, for the last 7 d of gestation), postnatal handling (maternal–offspring separation for 15 min per day during postnatal days 1–21), orboth. Prenatal stress reduced the number of NSCs derived from the subependyma of the lateral ventricle. The effect was already present at postnatal day 1 and persisted into adulthood (at least 14 months of age). Similarly, prenatal stress reduced in vivo proliferation in the adult subependyma of the lateral ventricle. Conversely, postnatal handling increased NSC number and reversed the effect of prenatal stress. The effects of prenatal stress on NSCs and proliferation and the effect of postnatal handling on NSCs did not differ between male and females. The findings demonstrate that environmental factors can produce changes in NSC number that are present at birth and endure into late adulthood. These changes may underlie some of the behavioral effects produced by prenatal stress and postnatal handling.
机译:产前压力对哺乳动物内分泌功能,脑形态和行为的许多影响可以通过短暂的产后分离和处理来逆转。我们已经检验了这样的假设:在神经发育的关键阶段,产前和产后经历的影响都由神经干细胞(NSC)数量的负向和正向调节介导。我们使用体外神经球蛋白测定法对经历过产前应激(孕产妇约束力每天持续2个小时,在妊娠的最后7天每天),产后处理(产后几天每天进行15分钟的母婴分离)的仓鼠中的NSC进行定量1–21),或两者皆有。产前压力减少了源于侧脑室室下膜的NSC的数量。该作用已在出生后第1天出现,并持续到成年期(至少14个月大)。同样,产前压力降低了侧脑室的成人室管膜下体内增殖。相反,产后处理增加了NSC数量并逆转了产前压力的影响。产前压力对NSCs和增殖的影响以及产后处理对NSCs的影响在男女之间没有差异。研究结果表明,环境因素会导致出生时存在的NSC数量变化,并持续到成年后期。这些变化可能是产前压力和产后处理所产生的某些行为影响的基础。

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