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MicroRNA profiling of diverse endothelial cell types
BACKGROUND: MicroRNAs are ~22-nt long regulatory RNAs that serve as critical modulators of post-transcriptional gene regulation. The diversity of miRNAs in endothelial cells (ECs) and the relationship of this diversity to epithelial and hematologic cells is unknown. We investigated the baseline miRN...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3223144/ https://www.ncbi.nlm.nih.gov/pubmed/22047531 http://dx.doi.org/10.1186/1755-8794-4-78 |
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author | McCall, Matthew N Kent, Oliver A Yu, Jianshi Fox-Talbot, Karen Zaiman, Ari L Halushka, Marc K |
author_facet | McCall, Matthew N Kent, Oliver A Yu, Jianshi Fox-Talbot, Karen Zaiman, Ari L Halushka, Marc K |
author_sort | McCall, Matthew N |
collection | PubMed |
description | BACKGROUND: MicroRNAs are ~22-nt long regulatory RNAs that serve as critical modulators of post-transcriptional gene regulation. The diversity of miRNAs in endothelial cells (ECs) and the relationship of this diversity to epithelial and hematologic cells is unknown. We investigated the baseline miRNA signature of human ECs cultured from the aorta (HAEC), coronary artery (HCEC), umbilical vein (HUVEC), pulmonary artery (HPAEC), pulmonary microvasculature (HPMVEC), dermal microvasculature (HDMVEC), and brain microvasculature (HBMVEC) to understand the diversity of miRNA expression in ECs. RESULTS: We identified 166 expressed miRNAs, of which 3 miRNAs (miR-99b, miR-20b and let-7b) differed significantly between EC types and predicted EC clustering. We confirmed the significance of these miRNAs by RT-PCR analysis and in a second data set by Sylamer analysis. We found wide diversity of miRNAs between endothelial, epithelial and hematologic cells with 99 miRNAs shared across cell types and 31 miRNAs unique to ECs. We show polycistronic miRNA chromosomal clusters have common expression levels within a given cell type. CONCLUSIONS: EC miRNA expression levels are generally consistent across EC types. Three microRNAs were variable within the dataset indicating potential regulatory changes that could impact on EC phenotypic differences. MiRNA expression in endothelial, epithelial and hematologic cells differentiate these cell types. This data establishes a valuable resource characterizing the diverse miRNA signature of ECs. |
format | Online Article Text |
id | pubmed-3223144 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-32231442011-11-24 MicroRNA profiling of diverse endothelial cell types McCall, Matthew N Kent, Oliver A Yu, Jianshi Fox-Talbot, Karen Zaiman, Ari L Halushka, Marc K BMC Med Genomics Research Article BACKGROUND: MicroRNAs are ~22-nt long regulatory RNAs that serve as critical modulators of post-transcriptional gene regulation. The diversity of miRNAs in endothelial cells (ECs) and the relationship of this diversity to epithelial and hematologic cells is unknown. We investigated the baseline miRNA signature of human ECs cultured from the aorta (HAEC), coronary artery (HCEC), umbilical vein (HUVEC), pulmonary artery (HPAEC), pulmonary microvasculature (HPMVEC), dermal microvasculature (HDMVEC), and brain microvasculature (HBMVEC) to understand the diversity of miRNA expression in ECs. RESULTS: We identified 166 expressed miRNAs, of which 3 miRNAs (miR-99b, miR-20b and let-7b) differed significantly between EC types and predicted EC clustering. We confirmed the significance of these miRNAs by RT-PCR analysis and in a second data set by Sylamer analysis. We found wide diversity of miRNAs between endothelial, epithelial and hematologic cells with 99 miRNAs shared across cell types and 31 miRNAs unique to ECs. We show polycistronic miRNA chromosomal clusters have common expression levels within a given cell type. CONCLUSIONS: EC miRNA expression levels are generally consistent across EC types. Three microRNAs were variable within the dataset indicating potential regulatory changes that could impact on EC phenotypic differences. MiRNA expression in endothelial, epithelial and hematologic cells differentiate these cell types. This data establishes a valuable resource characterizing the diverse miRNA signature of ECs. BioMed Central 2011-11-02 /pmc/articles/PMC3223144/ /pubmed/22047531 http://dx.doi.org/10.1186/1755-8794-4-78 Text en Copyright ©2011 McCall 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 | Research Article McCall, Matthew N Kent, Oliver A Yu, Jianshi Fox-Talbot, Karen Zaiman, Ari L Halushka, Marc K MicroRNA profiling of diverse endothelial cell types |
title | MicroRNA profiling of diverse endothelial cell types |
title_full | MicroRNA profiling of diverse endothelial cell types |
title_fullStr | MicroRNA profiling of diverse endothelial cell types |
title_full_unstemmed | MicroRNA profiling of diverse endothelial cell types |
title_short | MicroRNA profiling of diverse endothelial cell types |
title_sort | microrna profiling of diverse endothelial cell types |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3223144/ https://www.ncbi.nlm.nih.gov/pubmed/22047531 http://dx.doi.org/10.1186/1755-8794-4-78 |
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