Cargando…

Dynamic Activity of miR-125b and miR-93 during Murine Neural Stem Cell Differentiation In Vitro and in the Subventricular Zone Neurogenic Niche

Several microRNAs (miRNAs) that are either specifically enriched or highly expressed in neurons and glia have been described, but the identification of miRNAs modulating neural stem cell (NSC) biology remains elusive. In this study, we exploited high throughput miRNA expression profiling to identify...

Descripción completa

Detalles Bibliográficos
Autores principales: Lattanzi, Annalisa, Gentner, Bernhard, Corno, Daniela, Di Tomaso, Tiziano, Mestdagh, Pieter, Speleman, Frank, Naldini, Luigi, Gritti, Angela
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3694868/
https://www.ncbi.nlm.nih.gov/pubmed/23826292
http://dx.doi.org/10.1371/journal.pone.0067411
_version_ 1782274904584880128
author Lattanzi, Annalisa
Gentner, Bernhard
Corno, Daniela
Di Tomaso, Tiziano
Mestdagh, Pieter
Speleman, Frank
Naldini, Luigi
Gritti, Angela
author_facet Lattanzi, Annalisa
Gentner, Bernhard
Corno, Daniela
Di Tomaso, Tiziano
Mestdagh, Pieter
Speleman, Frank
Naldini, Luigi
Gritti, Angela
author_sort Lattanzi, Annalisa
collection PubMed
description Several microRNAs (miRNAs) that are either specifically enriched or highly expressed in neurons and glia have been described, but the identification of miRNAs modulating neural stem cell (NSC) biology remains elusive. In this study, we exploited high throughput miRNA expression profiling to identify candidate miRNAs enriched in NSC/early progenitors derived from the murine subventricular zone (SVZ). Then, we used lentiviral miRNA sensor vectors (LV.miRT) to monitor the activity of shortlisted miRNAs with cellular and temporal resolution during NSC differentiation, taking advantage of in vitro and in vivo models that recapitulate physiological neurogenesis and gliogenesis and using known neuronal- and glial-specific miRNAs as reference. The LV.miRT platform allowed us monitoring endogenous miRNA activity in low represented cell populations within a bulk culture or within the complexity of CNS tissue, with high sensitivity and specificity. In this way we validated and extended previous results on the neuronal-specific miR-124 and the astroglial-specific miR-23a. Importantly, we describe for the first time a cell type- and differentiation stage-specific modulation of miR-93 and miR-125b in SVZ-derived NSC cultures and in the SVZ neurogenic niche in vivo, suggesting key roles of these miRNAs in regulating NSC function.
format Online
Article
Text
id pubmed-3694868
institution National Center for Biotechnology Information
language English
publishDate 2013
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-36948682013-07-03 Dynamic Activity of miR-125b and miR-93 during Murine Neural Stem Cell Differentiation In Vitro and in the Subventricular Zone Neurogenic Niche Lattanzi, Annalisa Gentner, Bernhard Corno, Daniela Di Tomaso, Tiziano Mestdagh, Pieter Speleman, Frank Naldini, Luigi Gritti, Angela PLoS One Research Article Several microRNAs (miRNAs) that are either specifically enriched or highly expressed in neurons and glia have been described, but the identification of miRNAs modulating neural stem cell (NSC) biology remains elusive. In this study, we exploited high throughput miRNA expression profiling to identify candidate miRNAs enriched in NSC/early progenitors derived from the murine subventricular zone (SVZ). Then, we used lentiviral miRNA sensor vectors (LV.miRT) to monitor the activity of shortlisted miRNAs with cellular and temporal resolution during NSC differentiation, taking advantage of in vitro and in vivo models that recapitulate physiological neurogenesis and gliogenesis and using known neuronal- and glial-specific miRNAs as reference. The LV.miRT platform allowed us monitoring endogenous miRNA activity in low represented cell populations within a bulk culture or within the complexity of CNS tissue, with high sensitivity and specificity. In this way we validated and extended previous results on the neuronal-specific miR-124 and the astroglial-specific miR-23a. Importantly, we describe for the first time a cell type- and differentiation stage-specific modulation of miR-93 and miR-125b in SVZ-derived NSC cultures and in the SVZ neurogenic niche in vivo, suggesting key roles of these miRNAs in regulating NSC function. Public Library of Science 2013-06-27 /pmc/articles/PMC3694868/ /pubmed/23826292 http://dx.doi.org/10.1371/journal.pone.0067411 Text en © 2013 Lattanzi et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Lattanzi, Annalisa
Gentner, Bernhard
Corno, Daniela
Di Tomaso, Tiziano
Mestdagh, Pieter
Speleman, Frank
Naldini, Luigi
Gritti, Angela
Dynamic Activity of miR-125b and miR-93 during Murine Neural Stem Cell Differentiation In Vitro and in the Subventricular Zone Neurogenic Niche
title Dynamic Activity of miR-125b and miR-93 during Murine Neural Stem Cell Differentiation In Vitro and in the Subventricular Zone Neurogenic Niche
title_full Dynamic Activity of miR-125b and miR-93 during Murine Neural Stem Cell Differentiation In Vitro and in the Subventricular Zone Neurogenic Niche
title_fullStr Dynamic Activity of miR-125b and miR-93 during Murine Neural Stem Cell Differentiation In Vitro and in the Subventricular Zone Neurogenic Niche
title_full_unstemmed Dynamic Activity of miR-125b and miR-93 during Murine Neural Stem Cell Differentiation In Vitro and in the Subventricular Zone Neurogenic Niche
title_short Dynamic Activity of miR-125b and miR-93 during Murine Neural Stem Cell Differentiation In Vitro and in the Subventricular Zone Neurogenic Niche
title_sort dynamic activity of mir-125b and mir-93 during murine neural stem cell differentiation in vitro and in the subventricular zone neurogenic niche
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3694868/
https://www.ncbi.nlm.nih.gov/pubmed/23826292
http://dx.doi.org/10.1371/journal.pone.0067411
work_keys_str_mv AT lattanziannalisa dynamicactivityofmir125bandmir93duringmurineneuralstemcelldifferentiationinvitroandinthesubventricularzoneneurogenicniche
AT gentnerbernhard dynamicactivityofmir125bandmir93duringmurineneuralstemcelldifferentiationinvitroandinthesubventricularzoneneurogenicniche
AT cornodaniela dynamicactivityofmir125bandmir93duringmurineneuralstemcelldifferentiationinvitroandinthesubventricularzoneneurogenicniche
AT ditomasotiziano dynamicactivityofmir125bandmir93duringmurineneuralstemcelldifferentiationinvitroandinthesubventricularzoneneurogenicniche
AT mestdaghpieter dynamicactivityofmir125bandmir93duringmurineneuralstemcelldifferentiationinvitroandinthesubventricularzoneneurogenicniche
AT spelemanfrank dynamicactivityofmir125bandmir93duringmurineneuralstemcelldifferentiationinvitroandinthesubventricularzoneneurogenicniche
AT naldiniluigi dynamicactivityofmir125bandmir93duringmurineneuralstemcelldifferentiationinvitroandinthesubventricularzoneneurogenicniche
AT grittiangela dynamicactivityofmir125bandmir93duringmurineneuralstemcelldifferentiationinvitroandinthesubventricularzoneneurogenicniche