Chetty Sundari, Friedman Aaron R, Taravosh-Lahn Kereshmeh, Kirby Elizabeth D, Mirescu Christian, Guo Fuzheng, Krupik Danna, Nicholas Andrea, Geraghty Anna, Krishnamurthy Amrita, Tsai Meng-Ko, Covarrubias David, Wong Alana, Francis Darlene, Sapolsky Robert M, Palmer Theo D, Pleasure David, Kaufer Daniela
Helen Wills Neuroscience Institute, University of California, Berkeley, Berkeley, CA.
Department of Integrative Biology, University of California, Berkeley, Berkeley, CA.
Mol Psychiatry. 2014 Dec;19(12):1275-1283. doi: 10.1038/mp.2013.190. Epub 2014 Feb 11.
Stress can exert long-lasting changes on the brain that contribute to vulnerability to mental illness, yet mechanisms underlying this long-term vulnerability are not well understood. We hypothesized that stress may alter the production of oligodendrocytes in the adult brain, providing a cellular and structural basis for stress-related disorders. We found that immobilization stress decreased neurogenesis and increased oligodendrogenesis in the dentate gyrus (DG) of the adult rat hippocampus and that injections of the rat glucocorticoid stress hormone corticosterone (cort) were sufficient to replicate this effect. The DG contains a unique population of multipotent neural stem cells (NSCs) that give rise to adult newborn neurons, but oligodendrogenic potential has not been demonstrated in vivo. We used a nestin-CreER/YFP transgenic mouse line for lineage tracing and found that cort induces oligodendrogenesis from nestin-expressing NSCs in vivo. Using hippocampal NSCs cultured in vitro, we further showed that exposure to cort induced a pro-oligodendrogenic transcriptional program and resulted in an increase in oligodendrogenesis and decrease in neurogenesis, which was prevented by genetic blockade of glucocorticoid receptor (GR). Together, these results suggest a novel model in which stress may alter hippocampal function by promoting oligodendrogenesis, thereby altering the cellular composition and white matter structure.
应激可对大脑产生持久的变化,这会导致个体易患精神疾病,但这种长期易感性背后的机制尚未得到充分理解。我们推测,应激可能会改变成年大脑中少突胶质细胞的生成,为与应激相关的疾病提供细胞和结构基础。我们发现,成年大鼠海马齿状回(DG)的固定应激会减少神经发生并增加少突胶质细胞生成,并且注射大鼠糖皮质激素应激激素皮质酮(cort)足以复制这种效应。DG包含一群独特的多能神经干细胞(NSC),它们可产生成年新生神经元,但少突胶质细胞生成潜能尚未在体内得到证实。我们使用巢蛋白-CreER/YFP转基因小鼠品系进行谱系追踪,发现cort在体内可诱导表达巢蛋白的NSC发生少突胶质细胞生成。利用体外培养的海马NSC,我们进一步表明,暴露于cort会诱导一个促进少突胶质细胞生成的转录程序,并导致少突胶质细胞生成增加和神经发生减少,而糖皮质激素受体(GR)的基因阻断可防止这种情况发生。总之,这些结果提示了一种新模型,即应激可能通过促进少突胶质细胞生成来改变海马功能,从而改变细胞组成和白质结构。