Bag‐1 mediates glucocorticoid receptor trafficking to mitochondria after corticosterone stimulation: Potential role in regulating affective resilience

糖皮质激素受体 无血性 皮质酮 刺激 行为绝望测验 糖皮质激素 内分泌学 线粒体 内科学 生物 细胞生物学 医学 激素 海马体 多巴胺 抗抑郁药
作者
Shaolei Luo,Yangyang Hou,Ya‐Ping Zhang,Lei Feng,Richard Hunter,Peixiong Yuan,Yue Jia,Haoran Li,Gang Wang,Husseini K. Manji,Bruce S. McEwen,Chunjie Xiao,Hongkun Bao,Jing Du
出处
期刊:Journal of Neurochemistry [Wiley]
卷期号:158 (2): 358-372 被引量:20
标识
DOI:10.1111/jnc.15211
摘要

Molecular abnormalities within the Glucocorticoid Receptor (GR) stress signaling pathway involved in dysfunction of mitochondria and confer vulnerability to stress-related psychiatric disorders. Bcl-2 associated athanogene (Bag-1) is a target for the actions of mood stabilizers. Bag-1 interacts with GR, thereby regulating glucocorticoid function. In this study, we investigate the potential role of Bag-1 in regulating GR translocation into mitochondria. Corticosterone (CORT) treatment significantly enhanced Bag-1/GR complex formation and GR mitochondrial translocation in cultured rat cortical neurons after treatment for 30 min and 24 hr. By contrast, after stimulation with CORT for 3 days, localization of the Bag-1/GR complex and mitochondrial GR were reduced. Similar results were obtained in mice, in which administrated CORT in drinking water for 21 days significantly impaired the GR levels in the mitochondria, while Bag-1 over-expression rescued this reduction. Furthermore, chronic CORT exposure led to anhedonia-like and depression-like behaviors in the sucrose-consumption test and forced swimming test, and these behaviors were rescued by Bag-1 over-expression. These results suggest that Bag-1 mediates GR trafficking to mitochondria and regulates affective resilience in response to a CORT increase and provide potential insight into the mechanisms by which Bag-1 and GR could contribute to the physiology and pathogenesis of psychiatric disorders in response to the change of stress hormone.

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