Department of Anaesthesiology, Resuscitation, Emergency and Intensive Care Medicine, Faculty of Medicine, University of Rijeka, 51000 Rijeka, Croatia.
Anaesthesiology, Intensive Medicine and Pain Treatment Clinic, Clinical Hospital Centre Rijeka, 51000 Rijeka, Croatia.
Int J Mol Sci. 2023 Mar 1;24(5):4751. doi: 10.3390/ijms24054751.
Severe traumatic brain injury (sTBI) is an intracranial damage triggered by external force, most commonly due to falls and traffic accidents. The initial brain injury can progress into a secondary injury involving numerous pathophysiological processes. The resulting sTBI dynamics makes the treatment challenging and prompts the improved understanding of underlying intracranial processes. Here, we analysed how extracellular microRNAs (miRNAs) are affected by sTBI. We collected thirty-five cerebrospinal fluids (CSF) from five sTBI patients during twelve days (d) after the injury and combined them into d1-2, d3-4, d5-6 and d7-12 CSF pools. After miRNA isolation and cDNA synthesis with added quantification spike-ins, we applied a real-time PCR-array targeting 87 miRNAs. We detected all of the targeted miRNAs, with totals ranging from several nanograms to less than a femtogram, with the highest levels found at d1-2 followed by decreasing levels in later CSF pools. The most abundant miRNAs were miR-451a, miR-16-5p, miR-144-3p, miR-20a-5p, let-7b-5p, miR-15a-5p, and miR-21-5p. After separating CSF by size-exclusion chromatography, most miRNAs were associated with free proteins, while miR-142-3p, miR-204-5p, and miR-223-3p were identified as the cargo of CD81-enriched extracellular vesicles, as characterised by immunodetection and tunable resistive pulse sensing. Our results indicate that miRNAs might be informative about both brain tissue damage and recovery after sTBI.
严重创伤性脑损伤(sTBI)是由外力引起的颅内损伤,最常见的原因是跌倒和交通事故。最初的脑损伤可进展为涉及多种病理生理过程的继发性损伤。由此产生的 sTBI 动力学使得治疗具有挑战性,并促使人们更好地了解颅内过程。在这里,我们分析了细胞外 microRNAs(miRNAs)如何受到 sTBI 的影响。我们从五名 sTBI 患者中收集了 35 份脑脊液(CSF),并在损伤后 12 天(d)内将其分为 d1-2、d3-4、d5-6 和 d7-12 CSF 池。在 miRNA 分离和 cDNA 合成后,加入定量内标,我们应用了针对 87 个 miRNAs 的实时 PCR 阵列。我们检测到了所有靶向的 miRNAs,总浓度从几纳克到不到飞克不等,d1-2 时浓度最高,随后 CSF 池中的浓度逐渐降低。最丰富的 miRNAs 是 miR-451a、miR-16-5p、miR-144-3p、miR-20a-5p、let-7b-5p、miR-15a-5p 和 miR-21-5p。通过大小排阻色谱法分离 CSF 后,大多数 miRNAs 与游离蛋白相关,而 miR-142-3p、miR-204-5p 和 miR-223-3p 被鉴定为富含 CD81 的细胞外囊泡的货物,这是通过免疫检测和可调电阻脉冲感应来确定的。我们的结果表明,miRNAs 可能对 sTBI 后的脑组织损伤和恢复具有信息性。