4.4 Article

Activation of 6-8-week-old new mature adult-born dentate granule cells contributes to anxiety-like behavior

期刊

NEUROBIOLOGY OF STRESS
卷 15, 期 -, 页码 -

出版社

ELSEVIER SCIENCE INC
DOI: 10.1016/j.ynstr.2021.100358

关键词

Anxiety; New mature adult-born dentate granule cells; Hyperactivity; Learning and memory; Quiet property

资金

  1. National Natural Science Foundation of China [81601654]
  2. Natural Science Foundation of Guangdong Province, China [2014A030310090, 2016A030313578]
  3. Medical Scientific Research Foundation of Guangdong Province, China [A2015207]
  4. Pearl River S&T Nova Program of Guangzhou [201806010037]
  5. Scientific Research Foundation of Southern Medical University [PY2014N001, QD2015N001]

向作者/读者索取更多资源

The study reveals that sustained hyperactivity of 6-8-week-old new mature aDGCs induces anxiety-like behaviors and disrupts spatial memory, as well as activates mature DG neurons and inhibits immature aDGCs. Additionally, mice displaying anxiety-like behaviors due to chronic stress also show increased activity in 6-8-week-old aDGCs.
Adult-born dentate granule cells (aDGCs) at 4-6 weeks of age are particularly excitable but subsequently develop the quiet properties of mature cells. Most existing studies have focused on the hyperactivity of 4-6-week-old aDGCs or neurogenesis, which confers stress resilience or buffers stress responses. However, the function of the quiet property of new mature aDGCs remains unclear. Here we used a retrovirus expressing cre recombinase in combination with an associated-adenovirus to specifically interfere with the activity of new mature aDGCs, and estimated anxiety-like behaviors by the open-field test and elevated plus maze test, antidepressant-like behaviors by the tail suspension test, and spatial memory by the Barnes maze test. We found that sustained hyperactivity of 6-8-week-old, but not 8-10-week-old, aDGCs induced anxiety-like behaviors, and suppression of the activity of 6-8-week-old aDGCs disturbed spatial memory. Meanwhile, sustained hyperactivity of 6-8-week-old aDGCs induced activation of mature dentate gyrus (DG) neurons and inhibition of immature aDGCs. Additionally, the mice showing anxiety-like behaviors induced by chronic mild immobilization stress exhibited increased activity in 6-8-week-old aDGCs. Furthermore, the sustained hyperactivity of mature DG neurons also induced anxiety like behaviors and decreased the activity of immature aDGCs. Our results combined show that the excitation of 6-8-week-old new mature aDGCs, which prohibits them from normally entering the resting state, determines anxiety-like behavior, while the maintenance of normal excitation ability of 6-8-week-old new mature aDGCs confers memory. Our results suggests that strategies aimed at inhibiting unusual hyperactive new mature aDGCs at a restricted time window may protect against stress-related psychiatric disorders, such as anxiety and depression.

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