Li Yun, Zhang Bin, Yang Youhua, Su Ping, Samsom James Nicholas, Wong Albert H C, Liu Fang
Laboratory of Brain Disorders, Beijing Institute of Brain Disorders, Ministry of Science and Technology, Collaborative Innovation Center for Brain Disorders, Capital Medical University, Beijing 100054, China.
Oujiang Laboratory (Zhejiang Lab for Regenerative Medicine, Vision, and Brain Health), Institute of Mental Health and Drug Discovery, School of Mental Health, Wenzhou Medical University, Ouhai District, Wenzhou 325000, China.
Cells. 2024 Dec 10;13(24):2041. doi: 10.3390/cells13242041.
glucocorticoids may play an important role in the formation of fear memory, which is relevant to the neurobiology of post-traumatic stress disorder (PTSD). In our previous study, we showed the glucocorticoid receptor (GR) forms a protein complex with FKBP51, which prevents translocation of GR into the nucleus to affect gene expression; this complex is elevated in PTSD patients and by fear-conditioned learning in mice, and disrupting this complex blocks the storage and retrieval of fear-conditioned memories. The timing of release of glucocorticoid relative to the formation of a traumatic memory could be important in this process, and remains poorly understood.
we mapped serum corticosterone over time after fear conditioning in cardiac blood samples from male and female mice, as well as adult and aged mice using ELISA. We show a significant alteration in serum corticosterone after conditioning; notably, levels spike after 30 min but drop lower than unconditioned controls after 24 h. We further investigate the effect of glucocorticoid on GR phosphorylation and localization in HEK 293T cells by Western blot. Hydrocortisone treatment promotes phosphorylation and nuclear translocation of GR.
these data contribute to our understanding of the processes linking stress responses to molecular signals and fear memory, which is relevant to understanding the shared mechanisms related to PTSD.
糖皮质激素可能在恐惧记忆的形成中起重要作用,这与创伤后应激障碍(PTSD)的神经生物学有关。在我们之前的研究中,我们发现糖皮质激素受体(GR)与FKBP51形成一种蛋白质复合物,该复合物可阻止GR易位至细胞核以影响基因表达;这种复合物在PTSD患者中以及在小鼠的恐惧条件学习后会升高,破坏这种复合物会阻断恐惧条件记忆的存储和提取。在这个过程中,糖皮质激素相对于创伤性记忆形成的释放时间可能很重要,但目前仍了解不足。
我们使用酶联免疫吸附测定(ELISA)法,对雄性和雌性小鼠以及成年和老年小鼠心脏血液样本在恐惧条件训练后的不同时间点绘制血清皮质酮水平变化图。我们发现条件训练后血清皮质酮有显著变化;值得注意的是,水平在30分钟后达到峰值,但在24小时后降至低于未进行条件训练的对照组。我们通过蛋白质印迹法进一步研究糖皮质激素对人胚肾293T细胞中GR磷酸化和定位的影响。氢化可的松处理可促进GR的磷酸化和核转位。
这些数据有助于我们理解将应激反应与分子信号及恐惧记忆联系起来的过程,这对于理解与PTSD相关的共同机制具有重要意义。