Department of Genetics, Physical Anthropology and Animal Physiology, Faculty of Medicine and Nursing, University of The Basque Country (UPV/EHU), 48940, Leioa, Bizkaia, Spain.
BioCruces Bizkaia Health Research Institute, 48903, Barakaldo, Bizkaia, Spain.
Mol Neurobiol. 2020 Oct;57(10):4134-4142. doi: 10.1007/s12035-020-02011-3. Epub 2020 Jul 16.
The development of the human brain starts in the first weeks of embryo differentiation. However, there are many relevant neurodevelopmental processes that take place after birth and during lifespan. Such a fine and changing scenario requires the coordinated expression of thousands of genes to achieve the proper specialization and inter-connectivity. In this context, microRNAs (miRNAs), which can modulate mRNA stability and translation, are gaining recognition for their involvement in both brain development and neurodevelopmental disorders. Therefore, cerebrospinal fluid (CSF) miRNAs should be perfectly differentiated in relevant age periods. In this study, we aimed to highlight the biological variability of miRNA expression in the CSF throughout life, which is also crucial for biomarker discovery in CNS pathologies, especially in children, where they are desperately needed. We analyzed the CSF microRNAome of 14 healthy children (aged 0-7.4 years) by smallRNA-Seq and compared it with previously published data in adults (N = 7) and elders (N = 11). miR-423-5p and miR-22-3p were overexpressed in the < 1 and > 3 years groups, respectively. Additionally, we detected 18 miRNAs that reached their highest peak of expression at different time-points during the lifespan and sets of miRNAs that were exclusively expressed in a specific age group. On the contrary, miR-191-5p showed stable expression in CSF from the first year of life. Our results remark the complex differential miRNA expression profile that can be observed through life, which underlines the need for including appropriate age-matched controls when the expression of CSF miRNAs is analyzed in different pathological contexts. Graphical abstract.
人类大脑的发育始于胚胎分化的第一周。然而,有许多相关的神经发育过程发生在出生后和整个生命周期中。这种精细而不断变化的情况需要数千个基因的协调表达,以实现适当的专业化和相互连接。在这种情况下,microRNAs(miRNAs)可以调节 mRNA 的稳定性和翻译,它们在大脑发育和神经发育障碍中的作用越来越受到重视。因此,脑脊液(CSF)miRNAs应该在相关的年龄阶段得到完美区分。在这项研究中,我们旨在强调 miRNA 在整个生命周期中在 CSF 中的表达的生物学变异性,这对于中枢神经系统疾病的生物标志物发现也至关重要,特别是在儿童中,这些标志物非常需要。我们通过 smallRNA-Seq 分析了 14 名健康儿童(年龄 0-7.4 岁)的 CSF 微小 RNA 组,并将其与先前发表的成人(N=7)和老年人(N=11)的数据进行了比较。miR-423-5p 和 miR-22-3p 在<1 岁和>3 岁组中分别过表达。此外,我们还检测到了 18 种在生命过程中的不同时间点达到表达高峰的 miRNA,以及在特定年龄组中特异性表达的 miRNA 组。相反,miR-191-5p 在生命第一年的 CSF 中表达稳定。我们的研究结果表明,在整个生命周期中可以观察到复杂的差异表达 miRNA 谱,这强调了在不同病理情况下分析 CSF miRNAs 时需要包括适当的年龄匹配对照。