Visualization and quantitation of the expression of microRNAs and their target genes in neuroblastoma single cells using imaging cytometry

<p>Abstract</p> <p>Background</p> <p>MicroRNAs (miRNAs) are regulatory molecules that play an important role in many physiological processes, including cell growth, differentiation, and apoptosis. In addition to modulating normal cellular functions, it has also been rep...

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Main Authors: Ponomarev Eugene D, Veremeyko Tatiana, Barteneva Natasha S
Format: Article
Language:English
Published: BMC 2011-11-01
Series:BMC Research Notes
Subjects:
Online Access:http://www.biomedcentral.com/1756-0500/4/517
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spelling doaj-95fcfeaa7dec4e0181a7adf1b3f935d82020-11-25T01:46:26ZengBMCBMC Research Notes1756-05002011-11-014151710.1186/1756-0500-4-517Visualization and quantitation of the expression of microRNAs and their target genes in neuroblastoma single cells using imaging cytometryPonomarev Eugene DVeremeyko TatianaBarteneva Natasha S<p>Abstract</p> <p>Background</p> <p>MicroRNAs (miRNAs) are regulatory molecules that play an important role in many physiological processes, including cell growth, differentiation, and apoptosis. In addition to modulating normal cellular functions, it has also been reported that miRNAs are involved in the development of many pathologies, including cardiovascular diseases, cancer, inflammation, and neurodegeneration. Methods for the sensitive detection and measurement of specific miRNAs and their cellular targets are essential for both basic research endeavours, as well as diagnostic efforts aimed at understanding the role of miRNAs in disease processes.</p> <p>Findings</p> <p>In this study, we describe a novel, imaging cytometry-based protocol that allows for simultaneous visualisation and quantification of miRNAs and their putative targets. We validated this methodology in a neuronal cell line by examining the relationship of the miRNA miR-124 and its known target, cyclin dependent kinase 6 (CDK6). We found that ectopic overexpression of miR-124 resulted in the downregulation of CDK6, decreased cellular proliferation, and induced cellular morphological changes.</p> <p>Conclusions</p> <p>This method is suitable for analysing the expression and cellular localisation of miRNAs and target proteins in small cell subsets within a heterogeneous cell suspension. We believe that our cytometry-based methodology will be easily adaptable to miRNA studies in many areas of biomedical research including neuroscience, stem cell biology, immunology, and oncology.</p> http://www.biomedcentral.com/1756-0500/4/517MicroRNATarget geneImaging cytometryNeuroblastomaMiR-124CDK6
collection DOAJ
language English
format Article
sources DOAJ
author Ponomarev Eugene D
Veremeyko Tatiana
Barteneva Natasha S
spellingShingle Ponomarev Eugene D
Veremeyko Tatiana
Barteneva Natasha S
Visualization and quantitation of the expression of microRNAs and their target genes in neuroblastoma single cells using imaging cytometry
BMC Research Notes
MicroRNA
Target gene
Imaging cytometry
Neuroblastoma
MiR-124
CDK6
author_facet Ponomarev Eugene D
Veremeyko Tatiana
Barteneva Natasha S
author_sort Ponomarev Eugene D
title Visualization and quantitation of the expression of microRNAs and their target genes in neuroblastoma single cells using imaging cytometry
title_short Visualization and quantitation of the expression of microRNAs and their target genes in neuroblastoma single cells using imaging cytometry
title_full Visualization and quantitation of the expression of microRNAs and their target genes in neuroblastoma single cells using imaging cytometry
title_fullStr Visualization and quantitation of the expression of microRNAs and their target genes in neuroblastoma single cells using imaging cytometry
title_full_unstemmed Visualization and quantitation of the expression of microRNAs and their target genes in neuroblastoma single cells using imaging cytometry
title_sort visualization and quantitation of the expression of micrornas and their target genes in neuroblastoma single cells using imaging cytometry
publisher BMC
series BMC Research Notes
issn 1756-0500
publishDate 2011-11-01
description <p>Abstract</p> <p>Background</p> <p>MicroRNAs (miRNAs) are regulatory molecules that play an important role in many physiological processes, including cell growth, differentiation, and apoptosis. In addition to modulating normal cellular functions, it has also been reported that miRNAs are involved in the development of many pathologies, including cardiovascular diseases, cancer, inflammation, and neurodegeneration. Methods for the sensitive detection and measurement of specific miRNAs and their cellular targets are essential for both basic research endeavours, as well as diagnostic efforts aimed at understanding the role of miRNAs in disease processes.</p> <p>Findings</p> <p>In this study, we describe a novel, imaging cytometry-based protocol that allows for simultaneous visualisation and quantification of miRNAs and their putative targets. We validated this methodology in a neuronal cell line by examining the relationship of the miRNA miR-124 and its known target, cyclin dependent kinase 6 (CDK6). We found that ectopic overexpression of miR-124 resulted in the downregulation of CDK6, decreased cellular proliferation, and induced cellular morphological changes.</p> <p>Conclusions</p> <p>This method is suitable for analysing the expression and cellular localisation of miRNAs and target proteins in small cell subsets within a heterogeneous cell suspension. We believe that our cytometry-based methodology will be easily adaptable to miRNA studies in many areas of biomedical research including neuroscience, stem cell biology, immunology, and oncology.</p>
topic MicroRNA
Target gene
Imaging cytometry
Neuroblastoma
MiR-124
CDK6
url http://www.biomedcentral.com/1756-0500/4/517
work_keys_str_mv AT ponomareveugened visualizationandquantitationoftheexpressionofmicrornasandtheirtargetgenesinneuroblastomasinglecellsusingimagingcytometry
AT veremeykotatiana visualizationandquantitationoftheexpressionofmicrornasandtheirtargetgenesinneuroblastomasinglecellsusingimagingcytometry
AT bartenevanatashas visualizationandquantitationoftheexpressionofmicrornasandtheirtargetgenesinneuroblastomasinglecellsusingimagingcytometry
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