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FKBP5 相关 miRNA 特征作为新近创伤个体 PTSD 的潜在生物标志物。

FKBP5-associated miRNA signature as a putative biomarker for PTSD in recently traumatized individuals.

机构信息

Department of Life Science, Chung-Ang University, Seoul, South Korea.

Ewha Brain Institute, Ewha W. University, Seoul, South Korea.

出版信息

Sci Rep. 2020 Feb 25;10(1):3353. doi: 10.1038/s41598-020-60334-6.

Abstract

The epigenetic regulation of microRNA (miRNA) expression related to the FK506-binding protein 5 (FKBP5) gene may contribute to the risk of stress-related disorders such as posttraumatic stress disorder (PTSD). Here, we identified candidate miRNAs derived from FKBP5 knockout mice as a potential diagnostic biomarker of PTSD. Using a translational approach, candidate miRNAs found to alter in expression within the medial prefrontal cortex of FKBP5 knockout mice were selected. Each candidate miRNA was examined in the serum of 48 recently traumatized individuals with PTSD and 47 healthy individuals. Multimodal imaging was also conducted to identify the neural correlates for the expression of candidate exosomal miRNAs in response to trauma exposure. Differential miRNA expression was found according to PTSD diagnosis in two composite marker groups. The differential miRNA expression between the composite marker groups contributed to PTSD symptom severity, which may be explained by differential recruitment of prefrontolimbic activity in brain imaging. The present study reveals that a set of circulating exosomal miRNAs showing altered expression in FKBP5 knockout mice play a potential role as epigenetic markers of PTSD. The corroborative evidence from multiple levels including molecular, brain, and behavioral indicates that these epigenetic biomarkers may serve as complementary measures for the diagnosis and prognosis prediction of PTSD in recently traumatized individuals.

摘要

FK506 结合蛋白 5(FKBP5)基因的 miRNA 表达的表观遗传调控可能与应激相关障碍(如创伤后应激障碍(PTSD))的风险有关。在这里,我们鉴定了 FKBP5 敲除小鼠来源的候选 miRNA,作为 PTSD 的潜在诊断生物标志物。我们采用转化方法,选择了在 FKBP5 敲除小鼠的内侧前额叶皮层中表达改变的候选 miRNA。在 48 名新近遭受创伤的 PTSD 患者和 47 名健康个体的血清中检查了每个候选 miRNA。还进行了多模态成像,以鉴定候选外泌体 miRNA 在创伤暴露后表达的神经相关性。根据 PTSD 诊断,在两个复合标志物组中发现了 miRNA 表达的差异。复合标志物组之间的差异 miRNA 表达与 PTSD 症状严重程度相关,这可能通过大脑成像中前额叶边缘活动的差异招募来解释。本研究表明,一组在 FKBP5 敲除小鼠中表达改变的循环外泌体 miRNA 可能作为 PTSD 的表观遗传标志物发挥作用。包括分子、大脑和行为在内的多个层面的佐证证据表明,这些表观遗传生物标志物可能作为新近遭受创伤的个体 PTSD 诊断和预后预测的补充措施。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7705/7042218/117bb63a826e/41598_2020_60334_Fig1_HTML.jpg

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