ATF4
基因剔除小鼠
内分泌学
尾部悬挂试验
开阔地
内科学
生物
谷氨酸的
转录因子
综合应力响应
慢性应激
未折叠蛋白反应
谷氨酸受体
神经科学
细胞生物学
医学
行为绝望测验
信使核糖核酸
受体
基因
生物化学
海马体
抗抑郁药
内质网
翻译(生物学)
作者
Feixiang Yuan,Ziheng Zhou,Shangming Wu,Fuxin Jiao,Liang Chen,Leilei Fang,Hanrui Yin,Xiaoming Hu,Xiaoxue Jiang,Kan Liu,Fei Xiao,Haizhou Jiang,Shanghai Chen,Zhanju Liu,Yousheng Shu,Feifan Guo
标识
DOI:10.1073/pnas.2215590120
摘要
Chronic stress induces depression- and anxiety-related behaviors, which are common mental disorders accompanied not only by dysfunction of the brain but also of the intestine. Activating transcription factor 4 (ATF4) is a stress-induced gene, and we previously show that it is important for gut functions; however, the contribution of the intestinal ATF4 to stress-related behaviors is not known. Here, we show that chronic stress inhibits the expression of ATF4 in gut epithelial cells. ATF4 overexpression in the colon relieves stress-related behavioral alterations in male mice, as measured by open-field test, elevated plus-maze test, and tail suspension test, whereas intestine-specific ATF4 knockout induces stress-related behavioral alterations in male mice. Furthermore, glutamatergic neurons are inhibited in the paraventricular thalamus (PVT) of two strains of intestinal ATF4-deficient mice, and selective activation of these neurons alleviates stress-related behavioral alterations in intestinal ATF4-deficient mice. The highly expressed gut-secreted peptide trefoil factor 3 (TFF3) is chosen from RNA-Seq data from ATF4 deletion mice and demonstrated decreased in gut epithelial cells, which is directly regulated by ATF4. Injection of TFF3 reverses stress-related behaviors in ATF4 knockout mice, and the beneficial effects of TFF3 are blocked by inhibiting PVT glutamatergic neurons using DREADDs. In summary, this study demonstrates the function of ATF4 in the gut–brain regulation of stress-related behavioral alterations, via TFF3 modulating PVT neural activity. This research provides evidence of gut signals regulating stress-related behavioral alterations and identifies possible drug targets for the treatment of stress-related behavioral disorders.
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