Liao Jiangfeng, Zeng Guirong, Fang Wenting, Huang Weibin, Dai Xiaoman, Ye Qinyong, Zhang Jing, Chen Xiaochun
Department of Neurology, Fujian Institute of Geriatrics, Fujian Medical University Union Hospital, 29 Xinquan Road, Fuzhou, Fujian, 350001, China; Fujian Key Laboratory of Molecular Neurology, Institute of Neuroscience, Fujian Medical University, 88 Jiaotong Road, Fuzhou, Fujian, 350005, China.
Department of Neurology, Fujian Institute of Geriatrics, Fujian Medical University Union Hospital, 29 Xinquan Road, Fuzhou, Fujian, 350001, China; Fujian Key Laboratory of Molecular Neurology, Institute of Neuroscience, Fujian Medical University, 88 Jiaotong Road, Fuzhou, Fujian, 350005, China.
Physiol Behav. 2021 Jan 1;228:113197. doi: 10.1016/j.physbeh.2020.113197. Epub 2020 Oct 2.
The susceptibility to depression has been attributed to the chronic stress and genetic factors but still fails to identify definite biomarkers. The present study aimed to investigate the role of disrupted Notch signaling in the medial prefrontal cortex of the chronic social defeat stress (CSDS) mice and Wistar Kyoto (WKY) rats. RNA-sequencing and quantitative real-time PCR analyses evidenced the involvement of Notch signaling pathway in depression. Western blotting reported an increased level of Notch2 and NF-κB and a decreased level of Hes1 and Bcl2/Bax ratio both in the susceptible mice when compared with the control or resilient ones and in the depression WKY rats when compared with the Wistar or non-depression WKY groups. Further analysis showed that the above-mentioned changes were significantly correlated with the depression-like behaviors and that the elicited Notch2 strongly correlated with the upregulated NF-κB, not with the downregulated Hes1 or Bcl2/Bax ratio. In conclusion, the increased Notch2/NF-κB signaling in the medial prefrontal cortex may mediate depression susceptibility, providing a potential diagnostic biomarker or therapeutic target for treating major depressive disorder.
抑郁症的易感性被认为与慢性应激和遗传因素有关,但仍未能确定明确的生物标志物。本研究旨在探讨Notch信号通路紊乱在慢性社会挫败应激(CSDS)小鼠和Wistar Kyoto(WKY)大鼠内侧前额叶皮质中的作用。RNA测序和定量实时PCR分析证明Notch信号通路参与了抑郁症的发生。蛋白质免疫印迹法显示,与对照组或适应组相比,易感小鼠以及与Wistar组或非抑郁WKY组相比,抑郁WKY大鼠的Notch2和NF-κB水平升高,Hes1水平和Bcl2/Bax比值降低。进一步分析表明,上述变化与抑郁样行为显著相关,并且诱导的Notch2与上调的NF-κB强烈相关,而与下调的Hes1或Bcl2/Bax比值无关。总之,内侧前额叶皮质中Notch2/NF-κB信号通路的增加可能介导了抑郁症的易感性,为治疗重度抑郁症提供了潜在的诊断生物标志物或治疗靶点。