Department of Intensive Care Unit, Qinghai Provincial People's Hospital, Xining, 810007, China.
Department of Pathology, Qinghai Provincial People's Hospital, Xining, 810007, China.
Mil Med Res. 2019 Apr 30;6(1):12. doi: 10.1186/s40779-019-0203-z.
The aim of this work is to detect and compare the peripheral blood miRNA expression profiles in patients with severe traumatic brain injury (sTBI) 2, 12, 24, 48, and 72 h after injury at high altitude and to predict the target genes of differential expressed miRNAs.
Twenty sTBI patients from high-altitude areas were randomly selected according to the inclusion and exclusion criteria and were divided into five groups: the 2-h group, 12-h group, 24-h group, 48-h group, and 72-h group. Peripheral blood miRNA expression profiles were detected using real-time quantitative PCR (qRT-PCR).
The expression levels of miR-18a, miR-203, miR-146a, miR-149, miR-23b, and miR-let-7b in peripheral blood showed significant differences between the 2-h group and the 12-h group. The expression levels of miR-203, miR-146a, miR-149, miR-23b, and miR-let-7f in peripheral blood were up-regulated in the 24-h group. In the 48-h group, the expression levels of miR-181d, miR-29a, and miR-18b were upregulated. In the 72-h group, the expression levels of miR-203, miR-146a, miR-149, miR-23b, and miR-let-7f changed. The main target genes of the differentiation expressed miRNAs were genes that regulate inflammatory responses, apoptosis, and DNA damage/repair.
miRNAs may be involved in the pathogenesis of sTBI by dynamically regulating the target genes that regulate inflammatory responses, apoptosis, and DNA damage/repair pathways.
本研究旨在检测和比较高原地区重型颅脑损伤(sTBI)患者伤后 2、12、24、48 和 72 h 外周血 miRNA 表达谱,并预测差异表达 miRNA 的靶基因。
根据纳入和排除标准,随机选择 20 名来自高原地区的 sTBI 患者,并将其分为五组:2 h 组、12 h 组、24 h 组、48 h 组和 72 h 组。采用实时定量 PCR(qRT-PCR)检测外周血 miRNA 表达谱。
miR-18a、miR-203、miR-146a、miR-149、miR-23b 和 miR-let-7b 在 2 h 组和 12 h 组之间的外周血表达水平存在显著差异。miR-203、miR-146a、miR-149、miR-23b 和 miR-let-7f 在 24 h 组中的表达上调。miR-181d、miR-29a 和 miR-18b 在 48 h 组中表达上调。miR-203、miR-146a、miR-149、miR-23b 和 miR-let-7f 在 72 h 组中表达改变。分化表达 miRNA 的主要靶基因是调节炎症反应、细胞凋亡和 DNA 损伤/修复途径的基因。
miRNA 可能通过动态调节调节炎症反应、细胞凋亡和 DNA 损伤/修复途径的靶基因参与 sTBI 的发病机制。