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Identification of the microRNA networks contributing to macrophage differentiation and function
Limited evidence is available about the specific miRNA networks that regulate differentiation of specific immune cells. In this study, we characterized miRNA expression and associated alterations in expression with putative mRNA targets that are critical during differentiation of macrophages. In an...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5045358/ https://www.ncbi.nlm.nih.gov/pubmed/27119502 http://dx.doi.org/10.18632/oncotarget.8933 |
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author | Zhou, Hong Zhang, Jie Eyers, Fiona Xiang, Yang Herbert, Cristan Tay, Hock L. Foster, Paul S. Yang, Ming |
author_facet | Zhou, Hong Zhang, Jie Eyers, Fiona Xiang, Yang Herbert, Cristan Tay, Hock L. Foster, Paul S. Yang, Ming |
author_sort | Zhou, Hong |
collection | PubMed |
description | Limited evidence is available about the specific miRNA networks that regulate differentiation of specific immune cells. In this study, we characterized miRNA expression and associated alterations in expression with putative mRNA targets that are critical during differentiation of macrophages. In an effort to map the dynamic changes in the bone marrow (BM), we profiled whole BM cultures during differentiation into macrophages. We identified 112 miRNAs with expression patterns that were differentially regulated 5-fold or more during BMDM development. With TargetScan and MeSH databases, we identified 1267 transcripts involved in 30 canonical pathways linked to macrophage biology as potentially regulated by these specific 112 miRNAs. Furthermore, by employing miRanda and Ingenuity Pathways Analysis (IPA) analysis systems, we identified 18 miRNAs that are temporally linked to the expression of CSF1R, CD36, MSR1 and SCARB1; 7 miRNAs linked to the regulation of the transcription factors RUNX1 and PU.1, and 14 miRNAs target the nuclear receptor PPARα and PPARγ. This novel information provides an important reference resource for further study of the functional links between miRNAs and their target mRNAs for the regulation of differentiation and function of macrophages. |
format | Online Article Text |
id | pubmed-5045358 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-50453582016-10-13 Identification of the microRNA networks contributing to macrophage differentiation and function Zhou, Hong Zhang, Jie Eyers, Fiona Xiang, Yang Herbert, Cristan Tay, Hock L. Foster, Paul S. Yang, Ming Oncotarget Research Paper: Immunology Limited evidence is available about the specific miRNA networks that regulate differentiation of specific immune cells. In this study, we characterized miRNA expression and associated alterations in expression with putative mRNA targets that are critical during differentiation of macrophages. In an effort to map the dynamic changes in the bone marrow (BM), we profiled whole BM cultures during differentiation into macrophages. We identified 112 miRNAs with expression patterns that were differentially regulated 5-fold or more during BMDM development. With TargetScan and MeSH databases, we identified 1267 transcripts involved in 30 canonical pathways linked to macrophage biology as potentially regulated by these specific 112 miRNAs. Furthermore, by employing miRanda and Ingenuity Pathways Analysis (IPA) analysis systems, we identified 18 miRNAs that are temporally linked to the expression of CSF1R, CD36, MSR1 and SCARB1; 7 miRNAs linked to the regulation of the transcription factors RUNX1 and PU.1, and 14 miRNAs target the nuclear receptor PPARα and PPARγ. This novel information provides an important reference resource for further study of the functional links between miRNAs and their target mRNAs for the regulation of differentiation and function of macrophages. Impact Journals LLC 2016-04-22 /pmc/articles/PMC5045358/ /pubmed/27119502 http://dx.doi.org/10.18632/oncotarget.8933 Text en Copyright: © 2016 Zhou et al. http://creativecommons.org/licenses/by/2.5/ 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 credited. |
spellingShingle | Research Paper: Immunology Zhou, Hong Zhang, Jie Eyers, Fiona Xiang, Yang Herbert, Cristan Tay, Hock L. Foster, Paul S. Yang, Ming Identification of the microRNA networks contributing to macrophage differentiation and function |
title | Identification of the microRNA networks contributing to macrophage differentiation and function |
title_full | Identification of the microRNA networks contributing to macrophage differentiation and function |
title_fullStr | Identification of the microRNA networks contributing to macrophage differentiation and function |
title_full_unstemmed | Identification of the microRNA networks contributing to macrophage differentiation and function |
title_short | Identification of the microRNA networks contributing to macrophage differentiation and function |
title_sort | identification of the microrna networks contributing to macrophage differentiation and function |
topic | Research Paper: Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5045358/ https://www.ncbi.nlm.nih.gov/pubmed/27119502 http://dx.doi.org/10.18632/oncotarget.8933 |
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