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dc.contributor.authorPrieto Fernández, Endika
dc.contributor.authorLópez López, Elixabet ORCID
dc.contributor.authorMartín Guerrero, Idoia
dc.contributor.authorBárcena, Laura
dc.contributor.authorGonzález López, Monika
dc.contributor.authorAransay Bañares, Ana María
dc.contributor.authorLozano, Juan José
dc.contributor.authorBenito Fernández, Francisco Javier
dc.contributor.authorFalcón Pérez, Juan Manuel
dc.contributor.authorGarcía-Orad Carles, África ORCID
dc.date.accessioned2024-02-05T17:04:41Z
dc.date.available2024-02-05T17:04:41Z
dc.date.issued2020-07-16
dc.identifier.citationMolecular Neurobiology 57 : 4134-4142 (2020)es_ES
dc.identifier.issn1559-1182
dc.identifier.issn0893-7648
dc.identifier.urihttp://hdl.handle.net/10810/64652
dc.description.abstractThe development of 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 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. METHODS: 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). RESULTS: miR-423-5p and miR-22-3p were overexpressed in the <1 and >3 year groups, respectively. Additionally, we detected 18 miRNAs that reached their highest peak of expression at different time-points during 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. CONCLUSION: 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.es_ES
dc.description.sponsorshipThis work was supported by the Basque Government [IT989-16], the Spanish Ministry of Economy and Competitiveness MINECO [SAF2015-66312], and the Ramon Areces Foundation [FRA-17-JMF]. We thank MINECO for the TenTaCles (Spanish Excellence Network in Exosomes) and the Severo Ochoa Excellence Accreditation (SEV-2016-0644). Funding for open access charge: Severo Ochoa Excellence Accreditation (SEV-2016-0644).es_ES
dc.language.isoenges_ES
dc.publisherSpringeres_ES
dc.relationinfo:eu-repo/grantAgreement/MINECO/SAF2015-66312
dc.rightsinfo:eu-repo/semantics/openAccesses_ES
dc.subjectcerebrospinal fluides_ES
dc.subjectMicroRNAs
dc.subjectchildren
dc.subjectbiomarkers
dc.subjectbiological variability
dc.titleVariability in cerebrospinal fluid microRNAs through lifees_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.rights.holder© 2020, Springer Science Business Media, LLC, part of Springer Naturees_ES
dc.identifier.doi10.1007/s12035-020-02011-3
dc.departamentoesGenética, antropología física y fisiología animales_ES
dc.departamentoeuGenetika,antropologia fisikoa eta animalien fisiologiaes_ES


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