Department of Psychology, University of Otago, PO Box 56, Dunedin, 9054, New Zealand.
Brain Health Research Centre and Brain Research New Zealand, University of Otago, Dunedin, New Zealand.
Brain Struct Funct. 2018 Sep;223(7):3213-3228. doi: 10.1007/s00429-018-1685-2. Epub 2018 May 23.
Early during their maturation, adult-born dentate granule cells (aDGCs) are particularly excitable, but eventually develop the electrophysiologically quiet properties of mature cells. However, the stability versus plasticity of this quiet state across time and experience remains unresolved. By birthdating two populations of aDGCs across different animal ages, we found for 10-month-old rats the expected reduction in excitability across cells aged 4-12 weeks, as determined by Egr1 immunoreactivity. Unexpectedly, cells 35 weeks old (after genesis at an animal age of 2 months) were as excitable as 4-week-old cells, in the dorsal hippocampus. This high level of excitability at maturity was specific for cells born in animals 2 months of age, as cells born later in life did not show this effect. Importantly, excitability states were not fixed once maturity was gained, but were enhanced by enriched environment exposure or LTP induction, indicating that any maturational decrease in excitability can be compensated by experience. These data reveal the importance of the animal's age for aDGC excitability, and emphasize their prolonged capability for plasticity during adulthood.
在成熟早期,成年新生颗粒细胞(aDGC)特别容易兴奋,但最终会发展出成熟细胞的电生理安静特性。然而,这种安静状态在时间和经验上的稳定性与可塑性仍未得到解决。通过对不同动物年龄的两个 aDGC 群体进行标记,我们发现,对于 10 个月大的大鼠,正如 Egr1 免疫反应所确定的那样,4-12 周龄的细胞兴奋性会随着年龄的增长而降低。出乎意料的是,35 周龄的细胞(在 2 个月大的动物出生后)与 4 周龄的细胞一样容易兴奋,在背侧海马体中。这种成熟时的高兴奋性是 2 个月大的动物出生的细胞所特有的,因为后来出生的细胞没有表现出这种效应。重要的是,兴奋性状态一旦获得成熟就不会固定,而是会通过丰富环境暴露或 LTP 诱导增强,这表明任何成熟时兴奋性的降低都可以通过经验来补偿。这些数据揭示了动物年龄对 aDGC 兴奋性的重要性,并强调了它们在成年期的长期可塑性。