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

BACKGROUND: 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 ma...

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Autores principales: Ponomarev, Eugene D, Veremeyko, Tatiana, Barteneva, Natasha S
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3250958/
https://www.ncbi.nlm.nih.gov/pubmed/22123030
http://dx.doi.org/10.1186/1756-0500-4-517
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author Ponomarev, Eugene D
Veremeyko, Tatiana
Barteneva, Natasha S
author_facet Ponomarev, Eugene D
Veremeyko, Tatiana
Barteneva, Natasha S
author_sort Ponomarev, Eugene D
collection PubMed
description BACKGROUND: 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. FINDINGS: 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. CONCLUSIONS: 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.
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spelling pubmed-32509582012-01-05 Visualization and quantitation of the expression of microRNAs and their target genes in neuroblastoma single cells using imaging cytometry Ponomarev, Eugene D Veremeyko, Tatiana Barteneva, Natasha S BMC Res Notes Short Report BACKGROUND: 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. FINDINGS: 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. CONCLUSIONS: 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. BioMed Central 2011-11-28 /pmc/articles/PMC3250958/ /pubmed/22123030 http://dx.doi.org/10.1186/1756-0500-4-517 Text en Copyright ©2011 Ponomarev et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Short Report
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
title 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_short 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
topic Short Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3250958/
https://www.ncbi.nlm.nih.gov/pubmed/22123030
http://dx.doi.org/10.1186/1756-0500-4-517
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